Metal–Organic Frameworks (MOFs) and Covalent Organic Frameworks (COFs) Applied to Photocatalytic Organic Transformations

Among the different alternatives for catalysis using metal–organic frameworks (MOFs) or covalent organic frameworks (COFs), photocatalysis has remarkably evolved during the last decade. Photocatalytic reticular materials allowed recyclability and easy separation of catalyst from the product, also reaching the activity and selectivity commonly observed for molecular systems. Recently, photocatalytic MOFs and COFs have been applied to synthetic applications in order to obtain organic molecules of different complexity. However, although a good number of works have been devoted to this issue, an updated comprehensive revision on this field is still needed. The aim of this review was to fill this gap covering the following three general aspects: (1) common strategies on the design of reticular photocatalytic materials, (2) a comprehensive discussion of the photocatalytic organic reactions achieved by the use of COFs and MOFs, and (3) some critical considerations highlighting directions that should be considered in order to make advances in the study of photocatalytic COFs and MOFs.


Introduction
Chemistry has classically addressed questions related to how atoms are linked into molecules and how molecules interact and/or react with each other. Thus, remarkable achievements have been done in the study of molecules and polymers, but extended 2D and 3D structures remained underexplored until the beginning of this century. In order to fill this gap, over the last 20 years, a large effort has been devoted to applying concepts learned at the molecular level to the design of 2D and 3D materials. First, linkage of organic molecules and metal ions resulted in the formation of metal-organic frameworks (MOFs) [1]. Later, condensation of organic molecules allowed the isolation of covalent organic frameworks (COFs) [2]. Therefore, these developments offered an unprecedented research playground that can be described as the "chemistry beyond the molecule" and is nowadays known as reticular chemistry [3].
The opportunities that reticular chemistry offers are related to the following common features in this family of materials: (a) predesign of building blocks enables control over the frameworks geometries and chemical properties; (b) structural, thermal, and chemical stabilities can be tuned by modulating the strength of bonds that result in the propagation of frameworks, and (c) crystallinity makes possible      Among the applications of reticular materials, catalysis stands out for being fundamental in organic synthesis and commonly used for obtaining a wide variety of chemical products such as pharmaceutical or agrochemical compounds. From a practical point of view, heterogeneous catalysis is always a desirable approach, because it leads to recyclability and easy separation of the catalyst from the product [11]. In fact, the activity and selectivity achieved through homogeneous catalysis are not always feasible through heterogeneous systems. In this context, reticular chemistry offers new opportunities, because it allows the incorporation of complex molecular fragments into extended porous materials. So, design of molecular catalysts can boost the development of catalytic materials based on the reticular chemistry principles that put together the best of both homogeneous and heterogeneous worlds. A particularly interesting kind of catalysis, initially developed from a molecular perspective, is photocatalysis [12][13][14][15]. In this area, photocatalysts are structures able to harvest light energy to overcome kinetic and/or thermodynamic barriers, triggering, directing and accelerating reactions in presence of light that otherwise would be prohibitive. This approach is highly interesting, because of the potential use of sunlight as a clean and free source of energy. Therefore, visible-light photocatalysis using low energy/power irradiation systems is preferable to ultraviolet photocatalysis. In addition, photocatalysis can result on obtaining products with high economic relevance such as H 2 production to be used as fuel, CO 2 revalorization or the synthesis of complex organic molecules.
In some pathways commonly observed in photocatalysis, the light is absorbed by the photocatalyst, which in the excited state becomes a powerful oxidant or reducing agent or, in some cases, both [16]. Then, electron transfer processes result in the formation of transient radical species that eventually evolve towards the desired products or otherwise are involved in undesired side reactions ( Figure 3). Alternatively, the energy absorbed by the photocatalyst is directly transferred to a reagent (instead of promoting an electron transfer), resulting in its activation and then triggering the corresponding chemical process. Although the relationship between structure and photoactivity is not an obvious issue, two main requirements should be achieved: absorption of light at the appropriate wavelength and relaxation processes slower than activation of the desired reactions. A common way to reach these goals is the use of rigid highly conjugated organic structures [12]. Moieties with these characteristics can be readily incorporated into reticular materials. In particular, MOFs and COFs have allowed the inclusion of suitable π-units into their well-ordered extended structures that confer photocatalytic activity.
Catalysts 2020, 10, x FOR PEER REVIEW 4 of 44 Among the applications of reticular materials, catalysis stands out for being fundamental in organic synthesis and commonly used for obtaining a wide variety of chemical products such as pharmaceutical or agrochemical compounds. From a practical point of view, heterogeneous catalysis is always a desirable approach, because it leads to recyclability and easy separation of the catalyst from the product [11]. In fact, the activity and selectivity achieved through homogeneous catalysis are not always feasible through heterogeneous systems. In this context, reticular chemistry offers new opportunities, because it allows the incorporation of complex molecular fragments into extended porous materials. So, design of molecular catalysts can boost the development of catalytic materials based on the reticular chemistry principles that put together the best of both homogeneous and heterogeneous worlds. A particularly interesting kind of catalysis, initially developed from a molecular perspective, is photocatalysis [12][13][14][15]. In this area, photocatalysts are structures able to harvest light energy to overcome kinetic and/or thermodynamic barriers, triggering, directing and accelerating reactions in presence of light that otherwise would be prohibitive. This approach is highly interesting, because of the potential use of sunlight as a clean and free source of energy. Therefore, visible-light photocatalysis using low energy/power irradiation systems is preferable to ultraviolet photocatalysis. In addition, photocatalysis can result on obtaining products with high economic relevance such as H2 production to be used as fuel, CO2 revalorization or the synthesis of complex organic molecules.
In some pathways commonly observed in photocatalysis, the light is absorbed by the photocatalyst, which in the excited state becomes a powerful oxidant or reducing agent or, in some cases, both [16]. Then, electron transfer processes result in the formation of transient radical species that eventually evolve towards the desired products or otherwise are involved in undesired side reactions ( Figure 3). Alternatively, the energy absorbed by the photocatalyst is directly transferred to a reagent (instead of promoting an electron transfer), resulting in its activation and then triggering the corresponding chemical process. Although the relationship between structure and photoactivity is not an obvious issue, two main requirements should be achieved: absorption of light at the appropriate wavelength and relaxation processes slower than activation of the desired reactions. A common way to reach these goals is the use of rigid highly conjugated organic structures [12]. Moieties with these characteristics can be readily incorporated into reticular materials. In particular, MOFs and COFs have allowed the inclusion of suitable π-units into their well-ordered extended structures that confer photocatalytic activity.  From the reasons presented above, it can be inferred that MOFs and COFs represent a promising sustainable alternative to mediate photocatalytic processes. The possibility of fine tuning of their physicochemical properties through the design at the molecular level transferred to materials science open a wide range of opportunities in the design of light-harvesting antennae and photocatalytic systems. Photocatalytic applications of MOFs and COFs have been initially explored for artificial photosynthesis Catalysts 2020, 10, 720 5 of 45 and CO 2 reduction [17,18] or pollutant degradation processes [19]. These transformations are of undoubtable interest, owing to their environmental implications and, thus, is easy to understand why they attracted much attention during the last few years. As a consequence of this interest, some excellent reviews have been recently published overviewing the current state of the art of this field, in artificial photosynthesis and CO 2 reduction [18][19][20]. However, a more recent approach to the use of MOFs and COFs as photocatalytic materials consists of synthetic applications to achieve different organic transformations in order to obtain molecules of different complexity. Our exploration of the available literature revealed that a good number of reports have been devoted to this issue in the recent years. In contrast, there is a lack of an updated comprehensive review addressing the application of reticular chemistry to the photocatalytic synthesis of organic compounds. Thus, this review in intended to fill this gap presenting, first, the common strategies on the design of reticular photocatalytic materials related with their use in organic synthesis. Later, a comprehensive discussion of the reactions reported will be presented. Finally, some critical comparative considerations will be made, highlighting some factors that should be carefully taken into account on the study of such systems.

Strategies Applied on the Design of Photocatalytic MOFs and COFs
Metal-Organic Frameworks can combine the physicochemical properties of their organic and inorganic constituting parts because of their intrinsic hybrid nature. Both linkers and SBUs can act as isolated catalytic centers or, in the case of this review, as photosensitizer entities, enabling a wide range of photocatalytic organic transformations. Design of MOFs consist of the adequate combination of polytopic ligands and metal centers [1]. The most used kind of ligands are carboxylates. Typically, di-and tri-carboxylic ligands can adapt to a variety of coordination environments and materials topologies. Imidazolates are used to construct MOFs with zeolitic structures known as zeolitic imidazolate frameworks (ZIFs) [21]. Other nitrogen containing ligands, such as pyridinic compounds, are often used as pillar ligands, conferring an extra-stabilization to the 3D porous frameworks. The choice of metal center determines not only the structure but also the stability of the resulting MOF. Many metal centers have been employed in the field of MOFs, being very common the use of, for instance, zinc, zirconium, titanium, iron, and copper which are most representative of MOFs shown in this review. The different structural motifs of all the MOFs that have been employed as photocatalysts for organic reactions are represented in Figure 4.
In contrast with the straightforward strategies found for MOFs, more complex methodological issues should be considered in the design of photoactive COFs. Despite boron-containing COFs being initially reported by Yaghi et al. [2] in 2005 and representing the first successful isolation of this class of reticular materials, they did not present high stability because of their sensitivity towards the hydrolysis processes. This inconvenient has caused that photocatalytic applications of boroxineand boronate-based COFs to remain very scarce up to now. Thus, more stable-types of linkages, most of them devoted to the formation of C-N bonds, were lately employed in the construction of photoactive COFs. Among them, imines have a leading role [22]. They are synthesized through the condensation between amines and aldehydes (which are both readily accessible) in presence of a Bronsted or Lewis acid catalyst. Although their stability towards hydrolysis is higher, the presence of strong nucleophiles is still dangerous for the maintenance of their integrity. Therefore, different strategies have been developed in order to overcome this drawback such as the oxidation into amide bonds [23] or the formation of fully conjugated COFs [24]. β-Ketoenamine-based COFs, a special type derived from imine-based COFs, are also relevant since hydroxyl groups present in the aldehyde building block facilitate the condensation reaction, and the stability of the corresponding material is increased. Moreover, in regard to the field of photochemistry, this type of linkage results are quite interesting, because the lifetime of the triplet excited state is enhanced by the presence on keto-functionalities [25]. However, the first example where a COF was employed as heterogeneous photocatalyst consisted on the photoactivated hydrogen evolution reaction (HER) mediated by a hydrazone-based COF [26]. This type of linkage, formed by the condensation between hydrazides and Once these general considerations about MOFs and COFs are established, this review has categorized the following three different strategies that comprise the set of available reports devoted to the design of photocatalytically active reticular materials: (a) Pristine materials: are those MOFs or COFs composed solely by one structural backbone which does not contain attached functional molecules. The activity of these materials can be due to the intrinsic properties of the employed building blocks or can be the result of the combination of inactive building blocks that generates a photoactive framework.

Pristine Reticular Materials
First of all, the employment of pristine materials stands out for its simplicity: there is no need of functionalization protocols or incubation processes. In turn, several sub-strategies are recurrent in the design of this pristine frameworks.
On the one hand, for MOFs, the photocatalytic activity can be triggered by the SBUs or the metal nodes. In particular, the structural modification of the linker by the introduction of -NH2 groups is quite typical, because it enables the visible-light absorption in a wide variety of MOFs and allows the

Pristine Reticular Materials
First of all, the employment of pristine materials stands out for its simplicity: there is no need of functionalization protocols or incubation processes. In turn, several sub-strategies are recurrent in the design of this pristine frameworks.
On the one hand, for MOFs, the photocatalytic activity can be triggered by the SBUs or the metal nodes. In particular, the structural modification of the linker by the introduction of -NH 2 groups is Catalysts 2020, 10, 720 8 of 45 quite typical, because it enables the visible-light absorption in a wide variety of MOFs and allows the transference of electrons from the linkers to the metallic clusters [47]. In other cases, for example, Fe-O or Ti IV -O clusters present intrinsic photocatalytic activity towards the formation of reactive oxygen species, which can be used in energy transfer and electron transfer reactions [53,54]. Moreover, predesign and synthesis of intrinsically photoactive linkers (such as anthracene [36], triphenylamine [52], triazine [55], porphyrin [29], tetraphenylethylene [56], perylendiimide [57], benzoselenadiazole [58], and Ir/Ru-metal complexes [59]) are also important ( Figure 5).
Catalysts 2020, 10, x FOR PEER REVIEW  8 of 44 transference of electrons from the linkers to the metallic clusters [47]. In other cases, for example, Fe-O or Ti IV -O clusters present intrinsic photocatalytic activity towards the formation of reactive oxygen species, which can be used in energy transfer and electron transfer reactions [53,54]. Moreover, predesign and synthesis of intrinsically photoactive linkers (such as anthracene [36], triphenylamine [52], triazine [55], porphyrin [29], tetraphenylethylene [56], perylendiimide [57], benzoselenadiazole [58], and Ir/Ru-metal complexes [59]) are also important ( Figure 5). On the other hand, in the field of COFs, the use of pristine heterogeneous catalysts represents the most employed strategy for the design of this photocatalytically active materials. The same substrategies are observed in comparison with the field of MOFs. In this case, the enhanced electronic delocalization on conjugated organic frameworks has allowed the isolation of pristine materials with adequate photophysical properties for photocatalytic organic reactions.
A special type of conjugated porous organic polymers that present very similar characteristics to COFs are covalent triazine frameworks (CTFs). These polymeric materials are usually obtained from cyclotrimerization of aromatic nitriles under different specific conditions: using ionothermal synthesis, under the presence of strong acids, through Friedel-Crafts reaction or by amidinemediated procedures [60]. They present a long-term stability and are considered as an important family of heterogeneous catalysts for industrial purposes. Although most of the reported CTFs are generally amorphous, some crystalline and porous samples have been isolated, combining the necessary conditions to be considered as COFs. Therefore, CTFs are also included in this review. In addition, the contribution of CTFs to the field of organic photochemistry is quite important. In fact, some theoretical studies predicted the behavior of pristine CTFs as organic semiconductors, which, in combination with their structural versatility allows the fine tuning of their photophysical properties. Thus, CTFs are excellent candidates to be applied on the heterogeneous photocatalysis field [61]. However, it is important to differentiate between CTFs and triazine-containing COFs. While in CTFs, the triazine unit is formed during the solvothermal treatment, using as starting materials aromatic nitriles ( Figure 6, left), in triazine-containing COFs the triazine unit is preincorporated in the design of one of the constituting building blocks of the material, which will be formed by the condensation through one of the linkage types explained above (Figure 6, right). On the other hand, in the field of COFs, the use of pristine heterogeneous catalysts represents the most employed strategy for the design of this photocatalytically active materials. The same sub-strategies are observed in comparison with the field of MOFs. In this case, the enhanced electronic delocalization on conjugated organic frameworks has allowed the isolation of pristine materials with adequate photophysical properties for photocatalytic organic reactions.
A special type of conjugated porous organic polymers that present very similar characteristics to COFs are covalent triazine frameworks (CTFs). These polymeric materials are usually obtained from cyclotrimerization of aromatic nitriles under different specific conditions: using ionothermal synthesis, under the presence of strong acids, through Friedel-Crafts reaction or by amidine-mediated procedures [60]. They present a long-term stability and are considered as an important family of heterogeneous catalysts for industrial purposes. Although most of the reported CTFs are generally amorphous, some crystalline and porous samples have been isolated, combining the necessary conditions to be considered as COFs. Therefore, CTFs are also included in this review. In addition, the contribution of CTFs to the field of organic photochemistry is quite important. In fact, some theoretical studies predicted the behavior of pristine CTFs as organic semiconductors, which, in combination with their structural versatility allows the fine tuning of their photophysical properties. Thus, CTFs are excellent candidates to be applied on the heterogeneous photocatalysis field [61]. However, it is important to differentiate between CTFs and triazine-containing COFs. While in CTFs, the triazine unit is formed during the solvothermal treatment, using as starting materials aromatic nitriles (Figure 6, left), in triazine-containing COFs the triazine unit is pre-incorporated in the design of one of the constituting building blocks of the material, which will be formed by the condensation through one of the linkage types explained above (Figure 6, right).
Other organic materials that have been proven to be useful as photocatalysts are imine- [62], βketoenamine [25], and hydrazone [27] pristine COFs [24]. This sub-strategy would be equivalent to the observed intrinsic photocatalytic activity of SBUs or metal nodes in MOFs: the resultant photoactivity is caused by the combination of linkers and metal centers (in MOFs) or the condensation of building blocks (for COFs). Namely, the separated components of these reticular materials are not able to perform photocatalytic transformations. In other cases, a judicious predesign of photoactive building blocks has been also carried out, consisting on porphyrin [63], thiophene [64], triazine [65], benzoxazole [66], and triphenylamine units [67], among others ( Figure 7).

Functionalized Materials
The porous structure of reticular materials, in combination with the presence of electron-rich heteroatoms (such as O and N) and long π-conjugated surfaces has allowed the entrapment and functionalization of such organic frameworks with different photocatalysts by means of covalent bonds or supramolecular interactions.
In this sense, for MOFs, the covalent anchorage of different photosensitizers (Vitamin B2 [68], BODIPY [69], Eosin Y [70] or subphtalocyanine [71]) has allowed the obtaining of heterogeneous photocatalysts that generally present higher stability and photocatalytic activity than their homogeneous versions ( Figure 8). This enhancement can be due to the immobilization and isolation of photocatalytically active species, hampering unproductive encounters between photoexcited intermediates and, sometimes, leading to a change on the reaction mechanism.  Structural differences between covalent triazine frameworks (CTFs) and triazine-containing COFs.
Other organic materials that have been proven to be useful as photocatalysts are imine- [62], β-ketoenamine [25], and hydrazone [27] pristine COFs [24]. This sub-strategy would be equivalent to the observed intrinsic photocatalytic activity of SBUs or metal nodes in MOFs: the resultant photoactivity is caused by the combination of linkers and metal centers (in MOFs) or the condensation of building blocks (for COFs). Namely, the separated components of these reticular materials are not able to perform photocatalytic transformations. In other cases, a judicious predesign of photoactive building blocks has been also carried out, consisting on porphyrin [63], thiophene [64], triazine [65], benzoxazole [66], and triphenylamine units [67], among others ( Figure 7). Other organic materials that have been proven to be useful as photocatalysts are imine- [62], βketoenamine [25], and hydrazone [27] pristine COFs [24]. This sub-strategy would be equivalent to the observed intrinsic photocatalytic activity of SBUs or metal nodes in MOFs: the resultant photoactivity is caused by the combination of linkers and metal centers (in MOFs) or the condensation of building blocks (for COFs). Namely, the separated components of these reticular materials are not able to perform photocatalytic transformations. In other cases, a judicious predesign of photoactive building blocks has been also carried out, consisting on porphyrin [63], thiophene [64], triazine [65], benzoxazole [66], and triphenylamine units [67], among others ( Figure 7).

Functionalized Materials
The porous structure of reticular materials, in combination with the presence of electron-rich heteroatoms (such as O and N) and long π-conjugated surfaces has allowed the entrapment and functionalization of such organic frameworks with different photocatalysts by means of covalent bonds or supramolecular interactions.
In this sense, for MOFs, the covalent anchorage of different photosensitizers (Vitamin B2 [68], BODIPY [69], Eosin Y [70] or subphtalocyanine [71]) has allowed the obtaining of heterogeneous photocatalysts that generally present higher stability and photocatalytic activity than their homogeneous versions ( Figure 8). This enhancement can be due to the immobilization and isolation of photocatalytically active species, hampering unproductive encounters between photoexcited intermediates and, sometimes, leading to a change on the reaction mechanism.

Functionalized Materials
The porous structure of reticular materials, in combination with the presence of electron-rich heteroatoms (such as O and N) and long π-conjugated surfaces has allowed the entrapment and functionalization of such organic frameworks with different photocatalysts by means of covalent bonds or supramolecular interactions.
In this sense, for MOFs, the covalent anchorage of different photosensitizers (Vitamin B2 [68], BODIPY [69], Eosin Y [70] or subphtalocyanine [71]) has allowed the obtaining of heterogeneous photocatalysts that generally present higher stability and photocatalytic activity than their homogeneous versions ( Figure 8). This enhancement can be due to the immobilization and isolation of photocatalytically active species, hampering unproductive encounters between photoexcited intermediates and, sometimes, leading to a change on the reaction mechanism.
In this sense, for MOFs, the covalent anchorage of different photosensitizers (Vitamin B2 [68], BODIPY [69], Eosin Y [70] or subphtalocyanine [71]) has allowed the obtaining of heterogeneous photocatalysts that generally present higher stability and photocatalytic activity than their homogeneous versions ( Figure 8). This enhancement can be due to the immobilization and isolation of photocatalytically active species, hampering unproductive encounters between photoexcited intermediates and, sometimes, leading to a change on the reaction mechanism.  In the case of COFs, this strategy has only been explored in one case by our group, where Pt II -hydroxyquinoline complexes were immobilized and isolated as defects into the porous structure of an imine-based layered COF through monomer truncation strategy (Scheme 2) [72]. In the case of COFs, this strategy has only been explored in one case by our group, where Pt IIhydroxyquinoline complexes were immobilized and isolated as defects into the porous structure of an imine-based layered COF through monomer truncation strategy (Scheme 2) [72]. On another level, the encapsulation of both organic and inorganic homogeneous photocatalysts has also been explored for MOFs, as a result of different supramolecular interactions. For example, taking benefit from the adequate size of the pores and possible π-stacking interactions, Ru II and Au III complexes were occluded into ZIF and MOF structures, by Zhang [34] and Su [73], respectively ( Figure 9). In other case, Zhou [42] reported that the cationic [Ru(bpy)3] 2+ complex was entrapped in the anionic porous structure of PCN-99 MOF through ionic interactions.This sub-strategy has not been evaluated yet in obtaining photocatalytic COFs for organic transformations.

Hybrid Materials
The integration between reticular organic frameworks and different functional materials can give rise to new opportunities in the synthesis of interesting high-performance composites. These new hybrid materials can combine the abilities and properties of the different components, reaching different reactivity modes and interesting photophysical properties.
In particular, the combination between porous organic frameworks and metal-nanoparticles On another level, the encapsulation of both organic and inorganic homogeneous photocatalysts has also been explored for MOFs, as a result of different supramolecular interactions. For example, taking benefit from the adequate size of the pores and possible π-stacking interactions, Ru II and Au III complexes were occluded into ZIF and MOF structures, by Zhang [34] and Su [73], respectively ( Figure 9). In other case, Zhou [42] reported that the cationic [Ru(bpy) 3 ] 2+ complex was entrapped in the anionic porous structure of PCN-99 MOF through ionic interactions.This sub-strategy has not been evaluated yet in obtaining photocatalytic COFs for organic transformations. In the case of COFs, this strategy has only been explored in one case by our group, where Pt IIhydroxyquinoline complexes were immobilized and isolated as defects into the porous structure of an imine-based layered COF through monomer truncation strategy (Scheme 2) [72]. On another level, the encapsulation of both organic and inorganic homogeneous photocatalysts has also been explored for MOFs, as a result of different supramolecular interactions. For example, taking benefit from the adequate size of the pores and possible π-stacking interactions, Ru II and Au III complexes were occluded into ZIF and MOF structures, by Zhang [34] and Su [73], respectively ( Figure 9). In other case, Zhou [42] reported that the cationic [Ru(bpy)3] 2+ complex was entrapped in the anionic porous structure of PCN-99 MOF through ionic interactions.This sub-strategy has not been evaluated yet in obtaining photocatalytic COFs for organic transformations.

Hybrid Materials
The integration between reticular organic frameworks and different functional materials can give rise to new opportunities in the synthesis of interesting high-performance composites. These new hybrid materials can combine the abilities and properties of the different components, reaching different reactivity modes and interesting photophysical properties.

Hybrid Materials
The integration between reticular organic frameworks and different functional materials can give rise to new opportunities in the synthesis of interesting high-performance composites. These new hybrid materials can combine the abilities and properties of the different components, reaching different reactivity modes and interesting photophysical properties.
In particular, the combination between porous organic frameworks and metal-nanoparticles (NPs) is highly versatile. The variation of the nanoparticle composition, size, shape or environment implies a change on its absorption and emission properties, due to localized surface plasmon resonance (LSPR) phenomena [2]. The deposition of NPs on MOF or COFs surface can improve charge separation, driving electrons from the porous material to the nanoparticles, and increasing the photocatalytic efficiency. The obtaining of this type of hybrid materials can be performed through three different processes: (a) an in situ synthesis, where the material grows in presence of the NP-source; (b) an impregnation methodology, where the bulk material is immersed in a well-dispersed source of NPs; or (c) a controlled-reduction process, where molecular metal precursors are deposited and furtherly reduced to afford the desired NPs hybrid framework ( Figure 10).  On the one hand, in the field of MOFs, different examples of NPs-MOF as photocatalysts for organic transformations can be found, using various metal precursors: Au [74], Ni [75], Pd [76], Pt [77], Pd-Au [78], and Pd-Cu [79]. Most of them are devoted to their use as photocatalysts in the selective oxidation of benzylic alcohol and other oxidation processes (see in more detail below). Apart from MOF-NPs, other hybrid materials have been obtained in this field by using CdS quantum dots [80], bismuth ferrite [81], graphene oxide [82], fullerene C60 [83], and polyoxometalates [48] as composite partners.
On the other hand, in the field of COFs, only two hybrid materials have been evaluated as photocatalysts for organic transformations: MOF-COF and TiO2-COF composites, both reported by Wang's group [84,85]. In both cases, the strategy consists on using a NH2-functionalized material, in order to facilitate the covalent linkage between the MOF/TiO2 and the growing imine-based COF. Otherwise, no contributions of NPs-COF composites as photocatalyst for organic transformations have been reported up to now, but other applications, such as hydrogen production, CO2photoreduction or degradation of organic pollutants have been evaluated [9]. On the one hand, in the field of MOFs, different examples of NPs-MOF as photocatalysts for organic transformations can be found, using various metal precursors: Au [74], Ni [75], Pd [76], Pt [77], Pd-Au [78], and Pd-Cu [79]. Most of them are devoted to their use as photocatalysts in the selective oxidation of benzylic alcohol and other oxidation processes (see in more detail below). Apart from MOF-NPs, other hybrid materials have been obtained in this field by using CdS quantum dots [80], bismuth ferrite [81], graphene oxide [82], fullerene C 60 [83], and polyoxometalates [48] as composite partners.
On the other hand, in the field of COFs, only two hybrid materials have been evaluated as photocatalysts for organic transformations: MOF-COF and TiO 2 -COF composites, both reported by Wang's group [84,85]. In both cases, the strategy consists on using a NH 2 -functionalized material, in order to facilitate the covalent linkage between the MOF/TiO 2 and the growing imine-based COF. Otherwise, no contributions of NPs-COF composites as photocatalyst for organic transformations have been reported up to now, but other applications, such as hydrogen production, CO 2 -photoreduction or degradation of organic pollutants have been evaluated [9].

Oxidation Reactions
Photocatalytic oxidation reactions are chosen for the synthesis of a large number of molecules such as alcohols, epoxides, aldehydes, and ketones. Hazardous oxidizing reagents such as potassium permanganate and dichromate have traditionally been employed in the oxidation of different substrates, producing harmful byproducts. In contrast, aerobic oxidations are presented as an alternative. The development of heterogeneous photocatalytic systems using molecular oxygen as final oxidant leads to greener and more sustainable processes [11]. There are many examples of organic oxidation transformations carried out by MOFs or COFs, as we explain below.

Selective Oxidation of Alcohols
In the selective oxidation of alcohols to aldehydes or ketones, a mechanism based on the generation of superoxide radical anion is commonly reported (Scheme 3). In this case, the photocatalyst absorbs light, and in its excited state, separation of charges is produced, promoting electrons to the conduction band and generating holes in the valance band. These electrons activate O 2 to generate superoxide radical anion (O 2 −· ), which deprotonates benzyl alcohol obtaining hydroperoxide radical species (·OOH). Photogenerated holes are quenched by the benzoxide anion to oxidize it to its radical form, which subsequently reacts with ·OOH, generating benzaldehyde as the final product. H 2 O 2 is also usually produced. Although singlet oxygen is rarely reported, an energy transfer mechanism is observed in some photocatalytic materials, such as Bi-based MOFs. In this case, the presence of Bi suppresses the generation of O 2 −· and H 2 O 2 , being singlet oxygen the only active oxygen species [55].
generation of superoxide radical anion is commonly reported (Scheme 3). In this case, the photocatalyst absorbs light, and in its excited state, separation of charges is produced, promoting electrons to the conduction band and generating holes in the valance band. These electrons activate O2 to generate superoxide radical anion (O2 −· ), which deprotonates benzyl alcohol obtaining hydroperoxide radical species (·OOH). Photogenerated holes are quenched by the benzoxide anion to oxidize it to its radical form, which subsequently reacts with ·OOH, generating benzaldehyde as the final product. H2O2 is also usually produced. Although singlet oxygen is rarely reported, an energy transfer mechanism is observed in some photocatalytic materials, such as Bi-based MOFs. In this case, the presence of Bi suppresses the generation of O2 −· and H2O2, being singlet oxygen the only active oxygen species [55].
Photocatalytic oxidation of alcohols mediated by MOFs (Table 1): the first example using the design of linkers or SBUs with photoactive fragments was reported in 2011 by Wu [29]. A Sn IV -porphyrinbased MOF was capable of oxidizing 1,5-dihydroxynaphthalene to the corresponding quinone with full conversion. In 2012, an outstanding versatile amine-functionalized zirconium MOF, UiO-66-NH2 was used as photocatalyst in various oxidation reactions by Wang and coworkers. Although high catalyst loadings were needed, this report represents the first example where the introduction of amino groups into the constituting linkers of a MOF allowed its use as heterogeneous photocatalyst for several oxidation reactions [86]. This approach was later employed on a series of UiO-66-NH2 derivatives (consisting on mixed-linker zirconium-based MOFs synthesized through a one-pot procedure) which afforded the carbonylic products with moderate conversions [87]. Two years later, the variation of the photocatalytic activity of MIL-125 as a model platform was studied as a function of the presence of relative amounts of bdc-NH2 linkers. The oxidation of different alcohols was carried out in order to demonstrate that the maximum photocatalytic activity was achieved with a 50% of bdc-NH2, being the amination of all linkers in the MOF not required [88]. In 2019, another three examples employing this strategy were reported. Two bismuth-based MOFs, Bi-TATB and Bi-BTC, afforded the product in moderate conversions after 5 h [55]. On the other hand, a series of Ce-UiO-66 MOFs were synthesized with a solvent-free route, achieving the oxidation of alcohols under oxygen flux and near-ultraviolet light irradiation [89]. In addition, a further report demonstrated that was also possible the use of visible-light irradiation in these photocatalytic systems [90].
Photocatalyst Light irradiation Solvent Scheme 3. Generally accepted mechanism for the oxidation of alcohols. The proposed system consists of benzylic alcohol oxidation which has been the most explored system in the literature.

Scheme 3.
Generally accepted mechanism for the oxidation of alcohols. The proposed system consists of benzylic alcohol oxidation which has been the most explored system in the literature. (Table 1): the first example using the design of linkers or SBUs with photoactive fragments was reported in 2011 by Wu [29]. A Sn IV -porphyrin-based MOF was capable of oxidizing 1,5-dihydroxynaphthalene to the corresponding quinone with full conversion. In 2012, an outstanding versatile amine-functionalized zirconium MOF, UiO-66-NH 2 was used as photocatalyst in various oxidation reactions by Wang and coworkers. Although high catalyst loadings were needed, this report represents the first example where the introduction of amino groups into the constituting linkers of a MOF allowed its use as heterogeneous photocatalyst for several oxidation reactions [86]. This approach was later employed on a series of UiO-66-NH 2 derivatives (consisting on mixed-linker zirconium-based MOFs synthesized through a one-pot procedure) which afforded the carbonylic products with moderate conversions [87]. Two years later, the variation of the photocatalytic activity of MIL-125 as a model platform was studied as a function of the presence of relative amounts of bdc-NH 2 linkers. The oxidation of different alcohols was carried out in order to demonstrate that the maximum photocatalytic activity was achieved with a 50% of bdc-NH 2 , being the amination of all linkers in the MOF not required [88]. In 2019, another three examples employing this strategy were reported. Two bismuth-based MOFs, Bi-TATB and Bi-BTC, afforded the product in moderate conversions after 5 h [55]. On the other hand, a series of Ce-UiO-66 MOFs were synthesized with a solvent-free route, achieving the oxidation of alcohols under oxygen flux and near-ultraviolet light irradiation [89]. In addition, a further report demonstrated that was also possible the use of visible-light irradiation in these photocatalytic systems [90]. 1 Hyphen indicates that this value is not found in the original report.

Photocatalytic oxidation of alcohols mediated by MOFs
Another strategy used to synthesize MOFs capable of oxidizing different type of alcohols consists on the design of functionalization protocols. In 2018, a series of MOFs were structurally altered via post-synthetic modification by the condensation of benzaldehyde molecules with the pending amino groups on NH 2 -MIL-125(Ti). Under visible light irradiation, an enhancement of the photocatalytic activity was achieved by extending the conjugation through this post-synthetic process, carrying out the oxidation of aromatic alcohols with good results [91]. In 2019, the encapsulation of the photoactive [Ru(bpy) 3 ] 2+ complex into MIL-125-NH 2 cavities improved its photocatalytic activity in the oxidation of alcohols [92]. Following a different approach, Huang's group carried out the covalent anchorage and isolation of vitamin B 2 into UiO-66. Instead of generating superoxide radical anion via photoredox pathway (as observed for the homogeneous system), VB 2 @UiO-66 MOF was able to uniquely give rise to singlet oxygen through an energy transfer process. This effect is due to the immobilization and isolation of VB 2 , hampering triplet-triplet annihilation and increasing the stability of the photocatalyst [68].
Finally, the first reported example of hybrid structures of MOFs capable of performing this oxidation reaction is from 2014. Thus, Duan and coworkers carried out the encapsulation of Au nanoparticles into the porous structure of ZIF-8. The application of epitaxial growth strategy led to single-core shell structures, while the coalescence methodology gave rise to multi-core shell structures ( Figure 11). Au@ZIF-8 composites were employed as heterogeneous photocatalysts for the selective oxidation of a variety of alcohols into the corresponding aldehydes or ketones [74]. One year later, the group of Zhu presented a series of CdS-MIL-100(Fe) nanocomposites, formed by the superficial decoration of CdS quantum dots into the corresponding MOFs. The hybrid material presented enhanced photocatalytic activity in comparison with their separated components, because of the increased light absorption efficiency, its superior surface area and the easy charge separation and slow recombination rate. They were capable of oxidizing several alcohols with moderate conversions, reaching up to five consecutive recycling cycles [80]. In 2016, the impregnation of NH 2 -MIL-125(Ti) with nickel chloride as a metal source was performed by Zhu [75]. After a reducing treatment with NaBH 4 , Ni nanoparticles were formed. The corresponding Ni-doped NH 2 -MIL-125(Ti) was employed as heterogeneous photocatalyst in the selective oxidation of several aromatic alcohols, presenting an enhanced photocatalytic activity as a result of the synergistic effect between Ti-O clusters and Ni-NPs. In 2017, a series of MIL-LIC-1(Eu) graphene oxide composites MIL@GO were reported, yielding the final products with good conversions and short reaction times upon visible light irradiation and aqueous media. In this case, according to the authors, the molecular oxygen necessary for the transformation was generated in situ from water [82]. In 2019, the encapsulation and the deposition of copper nanoparticles on a copper-based UiO-66, Cu/Cu@UiO-66, was reported. This hybrid material achieved the corresponding oxidized products after 3 h in moderate conversions [93]. Very recently, a very active photocatalytic material has been reported by Yin [81]. The etching and regrowth process on a 3D MIL-53(Fe), that generates bismuth ferrite (BFO) nanosheets on its surface, was used as a strategy in order to avoid fast electron-hole recombination. photocatalytic activity was achieved by extending the conjugation through this post-synthetic process, carrying out the oxidation of aromatic alcohols with good results [91]. In 2019, the encapsulation of the photoactive [Ru(bpy)3] 2+ complex into MIL-125-NH2 cavities improved its photocatalytic activity in the oxidation of alcohols [92]. Following a different approach, Huang's group carried out the covalent anchorage and isolation of vitamin B2 into UiO-66. Instead of generating superoxide radical anion via photoredox pathway (as observed for the homogeneous system), VB2@UiO-66 MOF was able to uniquely give rise to singlet oxygen through an energy transfer process. This effect is due to the immobilization and isolation of VB2, hampering triplettriplet annihilation and increasing the stability of the photocatalyst [68].
Finally, the first reported example of hybrid structures of MOFs capable of performing this oxidation reaction is from 2014. Thus, Duan and coworkers carried out the encapsulation of Au nanoparticles into the porous structure of ZIF-8. The application of epitaxial growth strategy led to single-core shell structures, while the coalescence methodology gave rise to multi-core shell structures ( Figure 11). Au@ZIF-8 composites were employed as heterogeneous photocatalysts for the selective oxidation of a variety of alcohols into the corresponding aldehydes or ketones [74]. One year later, the group of Zhu presented a series of CdS-MIL-100(Fe) nanocomposites, formed by the superficial decoration of CdS quantum dots into the corresponding MOFs. The hybrid material presented enhanced photocatalytic activity in comparison with their separated components, because of the increased light absorption efficiency, its superior surface area and the easy charge separation and slow recombination rate. They were capable of oxidizing several alcohols with moderate conversions, reaching up to five consecutive recycling cycles [80]. In 2016, the impregnation of NH2-MIL-125(Ti) with nickel chloride as a metal source was performed by Zhu [75]. After a reducing treatment with NaBH4, Ni nanoparticles were formed. The corresponding Ni-doped NH2-MIL-125(Ti) was employed as heterogeneous photocatalyst in the selective oxidation of several aromatic alcohols, presenting an enhanced photocatalytic activity as a result of the synergistic effect between Ti-O clusters and Ni-NPs. In 2017, a series of MIL-LIC-1(Eu) graphene oxide composites MIL@GO were reported, yielding the final products with good conversions and short reaction times upon visible light irradiation and aqueous media. In this case, according to the authors, the molecular oxygen necessary for the transformation was generated in situ from water [82]. In 2019, the encapsulation and the deposition of copper nanoparticles on a copper-based UiO-66, Cu/Cu@UiO-66, was reported. This hybrid material achieved the corresponding oxidized products after 3 h in moderate conversions [93]. Very recently, a very active photocatalytic material has been reported by Yin [81]. The etching and regrowth process on a 3D MIL-53(Fe), that generates bismuth ferrite (BFO) nanosheets on its surface, was used as a strategy in order to avoid fast electron-hole recombination.  Photocatalytic oxidation of alcohols mediated by COFs ( Table 2): The use of COFs as photocatalysts in organic oxidation reactions is still underexplored and most of the works are very recent. The first report is dated to 2017, where an undecorated pristine thiophene-containing CTF (CTF-Th@SBA-15) was constructed using mesoporous silica as template. In this work, the performance of this heterogeneous photocatalyst was comparable to the most used non-metal-based catalysts reported up to that date, reaching a similar turnover frequency [64]. The only two examples of hybrid COFs as heterogeneous photocatalysts for synthetic organic transformations using as model reaction the oxidation of alcohols were reported by Wang and coworkers [85]. The first of them was devoted to the coating of TiO 2 nanobelts, with an imine-based COF, obtaining the hybrid material TiO 2 @COF-3. This material presents an enhanced photocatalytic activity due to the improvement on photon absorption related to the possibility of charge transfer from COF to TiO 2 . Such effect makes possible to perform benzylic alcohol oxidation under visible light irradiation. On the other hand, in 2020, a hybrid MOF-COF, NH 2 -MIL-125@TAPB-PDA-3, shown similar photocatalytic properties. In this case, amino groups of the previously synthesized MOF served as linking points to the growth of the imine-based COF [84]. Sulfoxides are very interesting compounds since they are prevalent structures in agriculture and pharmaceutical industries [94]. Thus, the selective oxidation of sulfides to sulfoxides is a recurrent model reaction in organic synthesis, since it allows to simply evaluate the photocatalytic activity of the new materials synthesized. Sulfoxidation also allows easy determination of chemoselectivity and to differentiate between the two possible mechanisms involved: an electron transfer or an energy transfer [62] (Scheme 4). On the one hand, in an electron transfer mediated mechanism, charge separation is produced in the photocatalyst under light irradiation. The generated holes oxidize the sulfide to its corresponding cationic radical and the photogenerated electrons reduce O 2 to O 2 −· . Finally, this active oxygen species reacts with the cationic radical intermediate, generating the persulfoxide species which reacts with a second sulfide to form two molecules of the final sulfoxide. On the other hand, energy transfer process can also take place under visible light irradiation, converting 3 O 2 into 1 O 2 through triplet-triplet annihilation between the triplet excited state of the catalytic fragment and 3 O 2 . Then, singlet oxygen reacts with the organic sulfide generating the same persulfoxide intermediate, which account for the formation of the corresponding sulfoxide product. The occurrence of one or another pathway can be precluded using selective scavengers (e.g., DABCO for singlet oxygen [95], 1,4-dimethoxybenzene for superoxide radical anion [96]). Such mechanistic probes have also been essayed for other oxidation processes. Interestingly, in many cases, there is not an exclusive pathway, and both mechanisms can be simultaneously operative. In some reports, the question of which mechanism produces the sulfoxide product is not addressed.
catalytic fragment and O2. Then, singlet oxygen reacts with the organic sulfide generating the same persulfoxide intermediate, which account for the formation of the corresponding sulfoxide product. The occurrence of one or another pathway can be precluded using selective scavengers (e.g., DABCO for singlet oxygen [95], 1,4-dimethoxybenzene for superoxide radical anion [96]). Such mechanistic probes have also been essayed for other oxidation processes. Interestingly, in many cases, there is not an exclusive pathway, and both mechanisms can be simultaneously operative. In some reports, the question of which mechanism produces the sulfoxide product is not addressed.
Light irradiation Solvent Scheme 4. Mechanism of oxidation of sulfides. At left, energy transfer mechanism, where singlet oxygen is the reactive oxygen species. At right, electron transfer mechanism, where superoxide radical anion is the reactive oxygen species. (Table 3): Focusing on the field of MOFs, there are some examples in which the design of linkers or SBUs with photoactive fragments is the chosen strategy. In 2011, the versatile Sn IV -porphyrin-based MOF previously presented in the alcohol oxidation part was also able to oxidize sulfides to sulfoxides with good results. In addition, the process became more selective by the immobilization of porphyrinic fragment (that acts as photosensitizer) into the porous framework, without overoxidation into sulfone product. In contrast, sulfone is found when the analogous molecular porphyrin was employed [29]. In the same year, Lin and coworkers reached the obtaining of bimetallated MOFs, by doping of UiO-67 with Ir, Re and Ru centers through the combination of both pre-synthesized metal-coordinated and naked linkers with Zr nodes. These doped MOFs were used as photocatalyst in the selective photosulfoxidation reaction, among other model test reactions, proposing an energy transfer mechanism [59]. Three years later, an anionic indium porphyrin framework, UNLPF-10, was capable of selectively oxidizing sulfides Scheme 4. Mechanism of oxidation of sulfides. At left, energy transfer mechanism, where singlet oxygen is the reactive oxygen species. At right, electron transfer mechanism, where superoxide radical anion is the reactive oxygen species.

Photocatalytic selective oxidation of sulfides mediated by MOFs
Photocatalytic selective oxidation of sulfides mediated by MOFs (Table 3): Focusing on the field of MOFs, there are some examples in which the design of linkers or SBUs with photoactive fragments is the chosen strategy. In 2011, the versatile Sn IV -porphyrin-based MOF previously presented in the alcohol oxidation part was also able to oxidize sulfides to sulfoxides with good results. In addition, the process became more selective by the immobilization of porphyrinic fragment (that acts as photosensitizer) into the porous framework, without overoxidation into sulfone product. In contrast, sulfone is found when the analogous molecular porphyrin was employed [29]. In the same year, Lin and coworkers reached the obtaining of bimetallated MOFs, by doping of UiO-67 with Ir, Re and Ru centers through the combination of both pre-synthesized metal-coordinated and naked linkers with Zr nodes. These doped MOFs were used as photocatalyst in the selective photosulfoxidation reaction, among other model test reactions, proposing an energy transfer mechanism [59]. Three years later, an anionic indium porphyrin framework, UNLPF-10, was capable of selectively oxidizing sulfides under low power visible light irradiation [31]. In 2019, three bimetallic Ir III -Zr IV MOFs were synthesized (Zr 6 -Irbpy, Zr 6 -IrbpyOMe, and Zr 6 -Irphen) by the combination of predesigned Ir-phenylpyridine complexes as ancillary linkers and Zr as metal nodes. Their extreme stability allowed the use of water as solvent in the sulfoxidation tests, observing a photoredox pathway as the preferred reaction mechanism. In addition, the Zr 6 -Irphen catalyst was recycled up to 10 times without losing its effectivity, neither its structural integrity ( Figure 12). [35]. The same exclusive photoredox activity was observed for an anthracene-based MOF, NNU-45, that was lately reported [36].  [83] synthesized (Zr6-Irbpy, Zr6-IrbpyOMe, and Zr6-Irphen) by the combination of predesigned Irphenylpyridine complexes as ancillary linkers and Zr as metal nodes. Their extreme stability allowed the use of water as solvent in the sulfoxidation tests, observing a photoredox pathway as the preferred reaction mechanism. In addition, the Zr6-Irphen catalyst was recycled up to 10 times without losing its effectivity, neither its structural integrity ( Figure 12). [35]. The same exclusive photoredox activity was observed for an anthracene-based MOF, NNU-45, that was lately reported [36]. The last example consists on a hybrid MOF obtained by the integration of guest C60 molecules and a porous porphyrin-based MOF, C60@PCN-222, which selectively achieved sulfoxides [83]. This composite takes advantage of the special properties of fullerene C60, due to the fact of its highly delocalized conjugated structure that accounts for the generation of reactive oxygen species. In particular, the high electron affinity of C60 is a key factor to enhance photoinduced charge separation with slow recombination. Thus, the combination of fullerenes with semiconductor MOFs resulted in an increased photocatalytic activity.  The last example consists on a hybrid MOF obtained by the integration of guest C 60 molecules and a porous porphyrin-based MOF, C 60 @PCN-222, which selectively achieved sulfoxides [83]. This composite takes advantage of the special properties of fullerene C 60 , due to the fact of its highly delocalized conjugated structure that accounts for the generation of reactive oxygen species. In particular, the high electron affinity of C 60 is a key factor to enhance photoinduced charge separation with slow recombination. Thus, the combination of fullerenes with semiconductor MOFs resulted in an increased photocatalytic activity.
Photocatalytic selective oxidation of sulfides mediated by COFs (Table 4): Our research group published in 2019 three different undecorated imine-based pristine materials: a layered-COF, a spherical-COF, and a 3D-COF that demonstrated photocatalytic activity in oxidation reactions. In particular, the oxidation of sulfides to sulfoxides efficiently proceeded using an ecofriendly mixture of solvents (ethanol and water) [62]. Remarkably, despite the use of water as a solvent, imine-based COFs were stable enough to perform several consecutive catalytic runs without losing activity. In the same year, two N,N'-bicarbazole-based CTFs, BC-CTF and Ph-BC-CTF, carried out the same oxidation reactions [97]. Very recently, a 2D and a 3D Pd-containing porphyrinic COFs, 2D-PdPor-COF and 3D-PdPor-COF, were capable of oxidizing the sulfides in very short reaction times (25 min), using low power visible light irradiation [98]. Also, a nanostructured COF, h-LZU1, which was obtained by using nanocrystals of ZIF-8 as template to yield capsule structures was obtained. This material was reported as photocatalytically active towards sulfoxidation under high power light UV-Visible irradiation with low recyclability and not complete selectivity [99]. Finally, our group reported the covalent in situ anchorage of photoactive Pt II -hydroxyquinoline complexes as defects into imine-based COFs, presenting TON up to 8000 and good stability and recyclability in comparison with molecular complex and pristine material [72].

Photocatalytic Dehydrogenation of Secondary Amines
The selective oxidative dehydrogenation of secondary amines to imines is feasible, due to the stability of the products and the impossibility of the substrates to generate nitriles. However, the substrate conversion is influenced by the steric hindrance around the N−H bond. In addition, the chemoselectivity for the oxidation of asymmetric dibenzylamines is often hampered because two different α-CH bonds can lead to distinct products. Therefore, examples of oxidation of symmetric dibenzylamines are common, while the selective oxidation of asymmetric dibenzylamines still remains challenging. The mechanism of the reaction has been reported for both reactive oxygen species, O 2 −· and 1 O 2 [46,73] (Scheme 5). In the first case, superoxide radical anion is concomitantly formed to the amine radical cation species. Such activated intermediates furtherly react triggering heterolytic cleavage, generating a mixture of benzaldehyde and benzylamine, which ultimately condensate to the corresponding imine. For the energy transfer mechanism, the singlet oxygen species directly reacts with the amine, provoking the subsequent heterolytic cleavage.  Photocatalytic oxidation of amines into imines mediated by COFs (Table 6): A very stable 2D porphyrin-containing COF, Por-sp 2 c-COF, was synthesized by Wang and collaborators [63] through Photocatalytic oxidation of amines into imines mediated by MOFs (Table 5): A pristine zinc-based MOF containing anthracene linkers as photosensitizers was reported in 2019, carrying out the photooxidation of secondary amines to the corresponding imines in short reaction times and great yields [46]. A different strategy, which is related to the encapsulation of photoactive Au complexes into the porous structure of two MOFs, was achieved by Su and collaborators. The isolation and immobilization of emissive Au Catalysts 2020, 10, 720 19 of 45 complexes into Au III @MOF1 and Au III @ZJU-28 resulted on the improvement of emission intensity, quantum yield, life-time of the excited state, and selective photocatalytic activity with respect to the complex in solution [73]. Table 5. Photooxidation reactions of secondary amines mediated by MOFs.

MOF Strategy Light Power (W) Reference
Secondary amines Anthracene 3D-MOF(Zn) Pristine >420 nm 300 [46] Secondary amines Au III @ZJU-28 Functionalization >300 nm 300 [73] Photocatalytic oxidation of amines into imines mediated by COFs (Table 6): A very stable 2D porphyrin-containing COF, Por-sp 2 c-COF, was synthesized by Wang and collaborators [63] through the Knoevenagel condensation, giving rise to a cyanovinylene-based COF. This material was firstly used to generate the imine products in only 30 min under low power visible light irradiation. In 2020, they also reported that the same Por-sp 2 c-COF was also capable of oxidizing secondary amines in combination with TEMPO as co-catalyst in 18 min using low-power red light source through a two-photon absorption mechanism [28].

Oxidation of Arylboronic Acids
The oxidation of arylboronic acids to phenols is known to proceed exclusively via superoxide radical anion [100]. Charge separation occurs in the photocatalyst under light irradiation, generating holes that oxidize a tertiary amine as sacrificial electron donor to its corresponding cationic radical and the photogenerated electrons reduce O 2 to O 2 −· . The transient reactive oxygen species directly reacts with arylboronic acid, forming an anionic radical intermediate. This radical species abstracts one hydrogen atom from the cationic oxidized amine. Finally, an irreversible rearrangement ion migration (OH − ) is subsequently followed by a hydrolysis affording the final phenol (see Scheme 6). Photocatalytic oxidation of arylboronic acids mediated by MOFs (Table 7): In 2015, two research groups, Matsuoka and Zhang, reported two different porphyrin-containing MOFs able to oxidize arylboronic acids to phenols. Zr-MOF-TCPP (also known as MOF-525) achieved the final phenol product under green LEDs irradiation using triethylamine as sacrificial electron donor [101]. In the other case, a family of UNLPF-MOFs were synthesized by variating the amount and the nature of the coordinated metal (Sn II , Sn IV or In III ). The photophysical properties of the materials synthesized were evaluated, and further translated into their application as photocatalyst in different organic transformations. As a result of this analysis, it was found that UNLPF-12 (which contains Sn IV coordinated to the porphyrin and In III as metal node) was the optimal photocatalyst for the oxidative hydroxylation of different substituted arylboronic acids [32].
other case, a family of UNLPF-MOFs were synthesized by variating the amount and the nature of the coordinated metal (Sn II , Sn IV or In III ). The photophysical properties of the materials synthesized were evaluated, and further translated into their application as photocatalyst in different organic transformations. As a result of this analysis, it was found that UNLPF-12 (which contains Sn IV coordinated to the porphyrin and In III as metal node) was the optimal photocatalyst for the oxidative hydroxylation of different substituted arylboronic acids [32].  [102]. In this case, the complex is covalently bonded to the material, since the linker contain bipyridine ligands. One year later, a different strategy was applied by Zhou [42], consisting on the occlusion of molecular [Ru(bpy)3] 2+ that stablished coulombic interactions with the anionic indium-based MOF, PCN-99. This functionalized framework was able to catalyze the oxidation of arylboronic acids, using also diisopropylethylamine (DIPEA) as sacrificial electron donor. Scheme 6. Mechanism of the photooxidation of arylboronic acids. Functionalization processes related to the different incorporation of [Ru(bpy) 3 ] 2+ complexes are also described in this reaction. In 2015, Cohen reported a UiO-67-based MOF with coordinated Ru centers (UiO-67-Ru(bpy) 3 ). This material was capable of oxidizing arylboronic acids under near-UV and visible light irradiation with DIPEA as sacrificial electron donor [102]. In this case, the complex is covalently bonded to the material, since the linker contain bipyridine ligands. One year later, a different strategy was applied by Zhou [42], consisting on the occlusion of molecular [Ru(bpy) 3 ] 2+ that stablished coulombic interactions with the anionic indium-based MOF, PCN-99. This functionalized framework was able to catalyze the oxidation of arylboronic acids, using also diisopropylethylamine (DIPEA) as sacrificial electron donor.
Photocatalytic oxidation of arylboronic acids mediated by COFs (Table 8): in 2018, three new benzoxazole-linked COFs, (LZU-190 to 192), were obtained by Wang and coworkers [66] through cascade-type reactions (see Figure 13). The initially imine-based formed COF evolved to the corresponding benzoxazole linkage thanks to the hydroxyl groups present in the amine-containing building block, conferring an outstanding stability to the material. This stability was confirmed by running until 20 photocatalytic cycles in the oxidation of phenylboronic acids to phenols with full conversion in each cycle. A different approach was employed in 2019, where an imine-linked COF was obtained through the self-condensation of a tetratopic building block, which contains both aldehydes and amino groups into its structure. The BBO-COF achieved the corresponding phenolic product with quite long reaction times [97]. Finally, three imine-based undecorated COFs with different architectures and morphologies carried out the oxidation of phenylboronic acid to phenol using a household white bulb as irradiating system with moderate yields, confirming the photoredox activity of these materials [62]. Photocatalytic oxidation of arylboronic acids mediated by COFs (Table 8): in 2018, three new benzoxazole-linked COFs, (LZU-190 to 192), were obtained by Wang and coworkers [66] through cascade-type reactions (see Figure 13). The initially imine-based formed COF evolved to the corresponding benzoxazole linkage thanks to the hydroxyl groups present in the amine-containing building block, conferring an outstanding stability to the material. This stability was confirmed by running until 20 photocatalytic cycles in the oxidation of phenylboronic acids to phenols with full conversion in each cycle. A different approach was employed in 2019, where an imine-linked COF was obtained through the self-condensation of a tetratopic building block, which contains both aldehydes and amino groups into its structure. The BBO-COF achieved the corresponding phenolic product with quite long reaction times [97]. Finally, three imine-based undecorated COFs with different architectures and morphologies carried out the oxidation of phenylboronic acid to phenol using a household white bulb as irradiating system with moderate yields, confirming the photoredox activity of these materials [62].  Other photocatalytic oxidation reactions mediated by MOFs (Table 9): In addition, there are some examples of oxidation reactions that have only been carried out using MOFs, remaining unexplored in the field of COFs. The first example dates from 2012, where large catalytic loadings of UiO-66-NH 2 were employed to achieve the oxidation of cyclohexane to cyclohexanone and epoxidation of cyclooctene and styrene derivatives. They described the mechanism of these transformations as an electron transfer process through the oxidation of the hydrocarbon concomitantly with superoxide radical anion formation. Such mixture of transient species eventually evolved to the corresponding products [86]. 1 Hyphen indicates that this value is not found in the original report.
In 2015, two pristine Fe-based MOFs, MIL-100(Fe) and MIL-68(Fe), were capable of oxidizing benzene to phenol using a mixture of acetonitrile and water as solvent and H 2 O 2 as reagent [54]. These MOFs produce the homolytic cleavage of hydrogen peroxide to generate active hydroxyl radicals (·OH) and the oxidation of Fe II centers, forming Fe III -OH species via photo-Fenton-like reaction. The hydroxyl radical attacks the benzene ring to form the hydroxycyclohexadienyl radical, that finally evolves to the phenol product through a hydrogen atom abstraction. This process also leads to the reduction of Fe III -OH into Fe II and the release of a water molecule, regenerating the original catalytic species (see Figure 14). 1 Hyphen indicates that this value was not found in the original report. (Table 9): In addition, there are some examples of oxidation reactions that have only been carried out using MOFs, remaining unexplored in the field of COFs. The first example dates from 2012, where large catalytic loadings of UiO-66-NH2 were employed to achieve the oxidation of cyclohexane to cyclohexanone and epoxidation of cyclooctene and styrene derivatives. They described the mechanism of these transformations as an electron transfer process through the oxidation of the hydrocarbon concomitantly with superoxide radical anion formation. Such mixture of transient species eventually evolved to the corresponding products [86].

Other photocatalytic oxidation reactions mediated by MOFs
In 2015, two pristine Fe-based MOFs, MIL-100(Fe) and MIL-68(Fe), were capable of oxidizing benzene to phenol using a mixture of acetonitrile and water as solvent and H2O2 as reagent [54]. These MOFs produce the homolytic cleavage of hydrogen peroxide to generate active hydroxyl radicals (·OH) and the oxidation of Fe II centers, forming Fe III -OH species via photo-Fenton-like reaction. The hydroxyl radical attacks the benzene ring to form the hydroxycyclohexadienyl radical, that finally evolves to the phenol product through a hydrogen atom abstraction. This process also leads to the reduction of Fe III -OH into Fe II and the release of a water molecule, regenerating the original catalytic species (see Figure 14). In 2019, the encapsulation of [Ru(bpy)3] 2+ into the porous structure of a ZIF was performed by Zhang [34]. It was achieved by the in-situ construction of the framework in presence of the mentioned complex, allowing the isolation of Ru(bpy)3@NKMOF-4. The photocatalytic activity of this functionalized material was evaluated using the oxidation of benzyl halides to the corresponding acetophenones as a model reaction (Scheme 7). As co-catalyst, 4-methoxypyridine was used, and Li2CO3 was added as a base under white light irradiation, resulting in the full conversion of various In 2019, the encapsulation of [Ru(bpy) 3 ] 2+ into the porous structure of a ZIF was performed by Zhang [34]. It was achieved by the in-situ construction of the framework in presence of the mentioned complex, allowing the isolation of Ru(bpy) 3 @NKMOF-4. The photocatalytic activity of this functionalized material was evaluated using the oxidation of benzyl halides to the corresponding acetophenones as a model reaction (Scheme 7). As co-catalyst, 4-methoxypyridine was used, and Li 2 CO 3 was added as a base under white light irradiation, resulting in the full conversion of various benzyl halides. They proposed a complex mechanistic landscape, in which the superoxide radical anion is involved, and the 4-methoxypyridine acts as electron transfer mediator.  Very recently, the generation of Pt nanoclusters supported on the surface of PCN-221 through photoreduction was achieved. This hybrid material was employed as photocatalyst for the oxidation of different N-alkyl(iso)quinolinium halides into the corresponding N-alkyl(iso)quinolones via singlet oxygen generation (Scheme 8) [77].

Scheme 7. Photooxidation of benzyl halides mediated by Ru(bpy)3@NKMOF-4.
Very recently, the generation of Pt nanoclusters supported on the surface of PCN-221 through photoreduction was achieved. This hybrid material was employed as photocatalyst for the oxidation of different N-alkyl(iso)quinolinium halides into the corresponding N-alkyl(iso)quinolones via singlet oxygen generation (Scheme 8) [77].  1 Hyphen indicates that this value is not found in the original report.

Oxidative Coupling
Oxidative couplings are classically catalyzed by a transition metal complex, like in typical crosscoupling reactions, although the mechanism changes because the oxidation process requires an oxidant to keep the entire process electroneutral [103]. In this sense, photocatalytic oxidative coupling reactions emerge as an alternative to make more sustainable processes than classical cross-coupling reactions. The two nucleophilic centers are often bound to hydrogen atoms, which makes possible hydrogen atom abstraction/transfer processes that are crucial in the general mechanism. The oxidative process transforms one of the nucleophiles into an electrophile, enabling the coupling between two molecules that were initially both of nucleophilic nature. The most common oxidant is O2 and the energy source consists on visible light in many cases, which fulfills the requirements of green chemistry. In particular, the selective oxidative coupling of amines to imine derivatives as important building blocks for the synthesis of fine chemicals and pharmaceuticals is highly desired. Photoinduced aerobic oxidation is the most sustainable and effective alternative under moderate conditions, avoiding high temperatures (~373 K) and high oxygen pressures (~5 atm) [104]. In almost all the reported works using reticular materials as photocatalysts, the reaction mechanism runs via electron transfer. However, there are a few published examples that proceed via energy transfer [33]. The electron transfer mechanism (Scheme 9, right) is initially triggered by the electrons promoted to Scheme 8. Photooxidation of N-alkyl(iso)quinolinium halides by Pt 0.9 @PCN-221.

Oxidative Coupling
Oxidative couplings are classically catalyzed by a transition metal complex, like in typical cross-coupling reactions, although the mechanism changes because the oxidation process requires an oxidant to keep the entire process electroneutral [103]. In this sense, photocatalytic oxidative coupling reactions emerge as an alternative to make more sustainable processes than classical cross-coupling reactions. The two nucleophilic centers are often bound to hydrogen atoms, which makes possible hydrogen atom abstraction/transfer processes that are crucial in the general mechanism. The oxidative process transforms one of the nucleophiles into an electrophile, enabling the coupling between two molecules that were initially both of nucleophilic nature. The most common oxidant is O 2 and the energy source consists on visible light in many cases, which fulfills the requirements of green chemistry. In particular, the selective oxidative coupling of amines to imine derivatives as important building blocks for the synthesis of fine chemicals and pharmaceuticals is highly desired. Photoinduced aerobic oxidation is the most sustainable and effective alternative under moderate conditions, avoiding high temperatures (~373 K) and high oxygen pressures (~5 atm) [104]. In almost all the reported works using reticular materials as photocatalysts, the reaction mechanism runs via electron transfer. However, there are a few published examples that proceed via energy transfer [33]. The electron transfer mechanism (Scheme 9, right) is initially triggered by the electrons promoted to the valence band of the photocatalyst, that are transferred to O 2 , generating superoxide radical anion (O 2 −· ).
Such process involves the generation of electron holes, that trigger the formation of the amine radical cation (regenerating the original form of the catalyst). Further evolution of this reactive species consists on a hydrogen atom abstraction from the amine radical cation, generating the iminium cation and HO 2 observed byproducts are the same, regardless of the mechanism. Some research has even reached the anaerobic version (Scheme 9, bottom), where protons act as oxidants, generating hydrogen as byproduct [105]. As a result of this electron transfer, electron holes are generated, which also trigger the formation of the amine radical cation transient species.  (Table 10): the most recurrent strategy consists in the design of linkers with photoactive fragments such as anthracene or porphyrin. In 2011, as previously presented in the sulfoxidation section, the doping of UiO-67-like MOFs was performed by Lin and coworkers, allowing the obtaining of bimetallated materials, which were used as photocatalyst in the oxidative coupling of primary benzylamines, among other oxidative transformations [59]. In 2015, a family of different metallated porphyrinic MOFs (see section about oxidation of arylboronic acids for further details) was described. In this case, UNLPF-12 provides a highly oxidative photoexcited state that efficiently performed the oxidative coupling of benzylamines [32]. In 2018, another porphyrinic MOF with Zr-oxo clusters (PCN-222) was reported, presenting comparable photocatalytic activity to the previous published works [104]. Later, two MOFs containing anthracene units as photosensitizers were obtained by Xing's group [36,46], and their photocatalytic activity was evaluated using the oxidative coupling of amines as a model reaction. In the first case, a 3D indium-based MOF (NNU-45) was employed [36], while in the other case, a zinc-based MOF was the chosen one [46]. In the same year, Duan and coworkers [33] obtained a family of Zn-based MOFs that contains different ratios of pyridine and methylpyridinium linkers, ZJU-56, capable of achieving C-N and C-C oxidative coupling reactions through two-photon absorption processes (see in CDC section). Otherwise, a ligand functionalization protocol of UiO-66 allowed the obtaining of different UiO-66-NH 2 MOFs, that enabled the isolation of the corresponding imine products under both aerobic and anaerobic conditions. [105]. There are also two recent examples of hybrid structures of MOFs capable of performing this organic transformation. In 2019, a MOF decorated with CdS quantum dots was reported (CdS@MIL-101). They obtained imine products from the oxidative coupling of primary amines. In addition, the same product was also obtained by the reaction of phenols with anilines, generating water instead of ammonia as byproduct [106]. Finally, very recently, a hybrid material with an optimal Pd nanocrystals loading, Pd/MIL-125-NH 2 , improved the benzylamine conversion rate of pristine MIL-125-NH 2 [76]. 1 Hyphen indicates that this value was not found in the original report.

Oxidative coupling reactions mediated by MOFs
Oxidative coupling reactions mediated by COFs (Table 11): only two very recent examples have been reported, related to the incorporation of photoactive building blocks into the COF structure in order to be used in this transformation. In the first case, a porphyrin-containing COF (Por-sp 2 c-COF) was obtained through the Knoevenagel condensation. It was employed as photocatalyst in combination with TEMPO as co-catalyst and oxygen as the terminal oxidant species, generating the coupling product in less than 30 min and using low power red light source [28]. On the other hand, a hydrazone-based COF (TFPT-BMTH) was reported for the oxidative coupling of benzylamine using water as solvent. It is an environmentally friendly process that has shown good recyclability of the catalyst to synthesize imines in good conversions after 24 h of irradiation [65]. It should be noticed that, for this reaction, the use of more stable materials is needed, especially in the field of COFs, since amines are employed as reagents. Apart from their basicity, they are well-known because of their nucleophilicity, which can lead to the destruction of the structural integrity of the material [107]. Thus, leaching and recyclability tests should be mandatory in this type of transformations, in order to ensure and reaffirm the heterogeneity of the catalyst and its stability.

Cross-Dehydrogenative Coupling
An important method to generate new C-C or C-Heteroatom bonds under mild conditions consists on the C-H bond cross-dehydrogenative coupling (CDC). Between all the possible CDC reactions, the functionalization of N-aryltetrahydroisoquinolines (THIQs) and other tertiary amines with different nucleophiles represents one of the most employed photocatalytic tests in order to evaluate the photoredox activity of a high variety of catalytic systems [108]. As coupling partners, a large variety of nucleophiles has been employed, such as malonates, nitriles, phosphites, and nitro-derivatives. The mechanism of this type of transformations has been widely studied [108]. In the case that the reaction proceeds under oxygen atmosphere, the oxygen will act as the terminal oxidant (Scheme 10). In general, the photoexcited catalytic material triggers the reduction of oxygen to superoxide radical anion species, generating the corresponding electron holes which are responsible of oxidation of THIQ into the amine radical cation. This superoxide radical anion can react with the previously generated amine radical cation in order to generate an iminium ion, which is highly electrophilic and reacts with a variety of nucleophiles. In some of the cases, the reaction proceeds in the absence of oxygen, but a super-stoichiometric amount of nitro-derivative as the terminal oxidant (which is also the nucleophile) is needed.

Cross-Dehydrogenative Coupling
An important method to generate new C-C or C-Heteroatom bonds under mild conditions consists on the C-H bond cross-dehydrogenative coupling (CDC). Between all the possible CDC reactions, the functionalization of N-aryltetrahydroisoquinolines (THIQs) and other tertiary amines with different nucleophiles represents one of the most employed photocatalytic tests in order to evaluate the photoredox activity of a high variety of catalytic systems [108]. As coupling partners, a large variety of nucleophiles has been employed, such as malonates, nitriles, phosphites, and nitroderivatives. The mechanism of this type of transformations has been widely studied [108]. In the case that the reaction proceeds under oxygen atmosphere, the oxygen will act as the terminal oxidant (Scheme 10). In general, the photoexcited catalytic material triggers the reduction of oxygen to superoxide radical anion species, generating the corresponding electron holes which are responsible of oxidation of THIQ into the amine radical cation. This superoxide radical anion can react with the previously generated amine radical cation in order to generate an iminium ion, which is highly electrophilic and reacts with a variety of nucleophiles. In some of the cases, the reaction proceeds in the absence of oxygen, but a super-stoichiometric amount of nitro-derivative as the terminal oxidant (which is also the nucleophile) is needed. Cross-dehydrogenative coupling reactions mediated by MOFs (Table 12): In the field of MOFs, there are various examples where this reaction has been employed in order to evaluate the photocatalytic activity of this type of materials. The preferred strategy consists on the design of photoactive linkers. For example, in 2011, Lin and coworkers [59] carried out the partial functionalization of UiO-67 constituted by dicarboxylic matching linkers containing Ir-phenylpyridine and Ru-bipyridine moieties. The UiO-67-doped presented high activity towards azaHenry reaction between N-aryl-THIQs and nitromethane as solvent. The different UiO-67-doped MOFs were also successfully employed as photocatalysts for CO 2 -photoreduction, and several oxidation reactions. Later, on 2015, Zhang et al. [32] reported the synthesis and photocatalytic applications of different UNLPF MOFs. In particular, UNLPF-12, which contains Sn IV -porphyrin as linker, was able to catalyze CDC between different N-aryl-THIQs and acetone as nucleophile. In 2016, Wang and collaborators reported the synthesis of UiO-68-mtpdc/etpdc, a MOF that contains tetraphenylethylene moieties as photosensitizers [56]. It was employed as photocatalyst for CDC reaction between N-aryl-THIQs and indole as nucleophilic coupling partner. Applying the same strategy, they also described the synthesis of UiO-68Se, which contains benzoselenadiazole units [58]. In this case, the nucleophile chosen was nitromethane, which was employed also as solvent. In 2019, He, Zhao and coworkers reported the synthesis of Cu-TPA MOF, which contains triphenylamine moieties as photosensitizers [52]. Cu-TPA presented moderated photocatalytic activity on aza-Henry reaction, being possible to recycle it up to 3 times. In the same year, Duan and collaborators presented ZJU-56 MOF [33] (Figure 15). It was constructed by mixing Zn II salts with dicarboxylic linkers containing different ratios of pyridine and hydroxypyridinium salts. Because of its cationic and N-atom rich structure, it resulted on a two-photon responsive MOF, which was employed as an efficient photocatalyst in the aza-Henry reaction, using nitromethane as nucleophile and solvent, and several N-aryl-THIQs with different substituents in the phenyl ring. Finally, very recently, Li Zhang and collaborators [109] reported the synthesis of two porphyrin-containing MOFs, Rh-and Ir-PCN224, and their application as photocatalysts for the construction of C-P bonds between N-aryl-THIQs and different phosphites through CDC reactions.
synthesis of UiO-68-mtpdc/etpdc, a MOF that contains tetraphenylethylene moieties as photosensitizers [56]. It was employed as photocatalyst for CDC reaction between N-aryl-THIQs and indole as nucleophilic coupling partner. Applying the same strategy, they also described the synthesis of UiO-68Se, which contains benzoselenadiazole units [58]. In this case, the nucleophile chosen was nitromethane, which was employed also as solvent. In 2019, He, Zhao and coworkers reported the synthesis of Cu-TPA MOF, which contains triphenylamine moieties as photosensitizers [52]. Cu-TPA presented moderated photocatalytic activity on aza-Henry reaction, being possible to recycle it up to 3 times. In the same year, Duan and collaborators presented ZJU-56 MOF [33] ( Figure  15). It was constructed by mixing Zn II salts with dicarboxylic linkers containing different ratios of pyridine and hydroxypyridinium salts. Because of its cationic and N-atom rich structure, it resulted on a two-photon responsive MOF, which was employed as an efficient photocatalyst in the aza-Henry reaction, using nitromethane as nucleophile and solvent, and several N-aryl-THIQs with different substituents in the phenyl ring. Finally, very recently, Li Zhang and collaborators [109] reported the synthesis of two porphyrin-containing MOFs, Rh-and Ir-PCN224, and their application as photocatalysts for the construction of C-P bonds between N-aryl-THIQs and different phosphites through CDC reactions. The functionalization strategy has also been applied in obtaining MOFs with photocatalytic activity for CDC reactions. Thus, a BODIPY photosensitizer was anchored to UiO-68 through pending amino groups present in the linkers [69]. The UiO-68-BP was employed as heterogeneous photocatalyst for CDC reactions among different N-aryl-THIQs and different nitroalkanes. The same strategy was later employed by Khan and collaborators [70], who anchored the organic photocatalyst The functionalization strategy has also been applied in obtaining MOFs with photocatalytic activity for CDC reactions. Thus, a BODIPY photosensitizer was anchored to UiO-68 through pending amino groups present in the linkers [69]. The UiO-68-BP was employed as heterogeneous photocatalyst for CDC reactions among different N-aryl-THIQs and different nitroalkanes. The same strategy was later employed by Khan and collaborators [70], who anchored the organic photocatalyst Eosin Y into UiO-66-NH 2 through amide bonds. The EY@UiO-66-NH 2 MOF was employed as photocatalyst in CDC reactions among different tertiary amines (not only THIQs) and various nucleophiles such as nitriles, phosphites, naphtols, malonates, and ketones. 1 Hyphen indicates that this value was not found in the original report.
Cross-dehydrogenative coupling reactions mediated by COFs (Table 13): In the field of COFs, this reaction has been scarcely explored. The two first examples of COFs as photocatalytic materials for organic transformations studied CDC as a proposed model reaction. Initially, at the end of 2016, Wu [27] employed a pristine acylhydrazone-based COF, TFB-COF, as photocatalyst for CDC reaction between different N-aryl-THIQs and various nucleophiles (i.e., ketones and nitro-derivatives). Almost at the same time, in 2017, Liu and collaborators [110] presented the applicability of COF-JLU5, an imine-based COF which contains triazine units, as heterogeneous photocatalyst in the same reaction, but with a wider scope of THIQs and nucleophiles (phosphite and malonates were added), and lower reaction times. Finally, two bidimensional imine-based COFs that contain triphenylamine and tetraphenylethylene units as photosensitizers were synthesized by Cui and coworkers [67]. They presented high photoredox activity for debromination and CDC reactions. Specifically, the CDC reaction between different N-aryl-THIQs and nitromethane as a coupling partner was efficiently catalyzed by both COFs. N-arylTHIQs/nitromethane COF-1, COF-2 (imine-based) Pristine (photoactive building blocks) White LEDs - [67] 1 Hyphen indicates that this value was not found in the original report.

Dehalogenation
Organic halides are commonly used on organic synthesis because they are readily accessible and useful for obtaining different high-added value products. For instance, they can account for radical formation under light irradiation, resulting on C-C coupling of different nature. However, most brominated compounds are also considered as persistent pollutants. For example, polybrominated diphenylethers (PBDEs), which are frequently used as flame retardants in polymers and plastics, are demanded worldwide, but they are bioaccumulative and toxic [111]. Photocatalysis has emerged as a possible way to the remediation of this type of compounds through radical-involved reactions, such as photoreductive dehalogenation, where the halogen atom is substituted by a hydrogen atom [112]. Another method consists on the α-alkylation of aldehydes where the formed radical is trapped by an enamine intermediate which after the catalytic cycle and hydrolysis allows the formation of the alkylated product. [113]. In both cases, a reductive quenching of the excited state of the photocatalyst by the organic halide is observed, that allows the formation of the desired radical (Scheme 11). This radical will capture a hydrogen atom from the reaction medium (in the case of the photoreductive dehalogenation) or will be trapped by a strong electrophile such as an iminium ion (in the case of the alkylation of aldehydes). diphenylethers (PBDEs), which are frequently used as flame retardants in polymers and plastics, are demanded worldwide, but they are bioaccumulative and toxic [111]. Photocatalysis has emerged as a possible way to the remediation of this type of compounds through radical-involved reactions, such as photoreductive dehalogenation, where the halogen atom is substituted by a hydrogen atom [112]. Another method consists on the α-alkylation of aldehydes where the formed radical is trapped by an enamine intermediate which after the catalytic cycle and hydrolysis allows the formation of the alkylated product. [113]. In both cases, a reductive quenching of the excited state of the photocatalyst by the organic halide is observed, that allows the formation of the desired radical (Scheme 11). This radical will capture a hydrogen atom from the reaction medium (in the case of the photoreductive dehalogenation) or will be trapped by a strong electrophile such as an iminium ion (in the case of the alkylation of aldehydes).  (Table 14): The most recurrent strategies in the construction of MOFs for dehalogenation processes consist not only on the design of photoactive linkers or clusters, but also on the functionalization and immobilization of organic and inorganic dyes through different interactions. The first example of dehalogenation in the field of MOFs was reported by Duan and coworkers in 2012, where Zn-PYI1 and Zn-PYI2 (enantiomers) were synthesized through the combination of a triphenylamine linker (the photosensitizer) with a chiral anchored amino-organocatalyst and Zn as the metal source [114] (Figure 16). These two MOFs were employed as bifunctional organo-photocatalyst in the asymmetric α-alkylation of aldehydes. As organic halide, diethylbromomalonate was employed, and it was combined with different aliphatic aldehydes in the presence of 2,6-lutidine as a base. Excellent enantiomeric excesses and yields were reached, being possible to isolate the two enantiomeric products by using one MOF or another. In addition, sizediscrimination studies were performed. Scheme 11. Generally accepted mechanism of dehalogenation reactions. (Table 14): The most recurrent strategies in the construction of MOFs for dehalogenation processes consist not only on the design of photoactive linkers or clusters, but also on the functionalization and immobilization of organic and inorganic dyes through different interactions. The first example of dehalogenation in the field of MOFs was reported by Duan and coworkers in 2012, where Zn-PYI1 and Zn-PYI2 (enantiomers) were synthesized through the combination of a triphenylamine linker (the photosensitizer) with a chiral anchored amino-organocatalyst and Zn as the metal source [114] (Figure 16). These two MOFs were employed as bifunctional organo-photocatalyst in the asymmetric α-alkylation of aldehydes. As organic halide, diethylbromomalonate was employed, and it was combined with different aliphatic aldehydes in the presence of 2,6-lutidine as a base. Excellent enantiomeric excesses and yields were reached, being possible to isolate the two enantiomeric products by using one MOF or another. In addition, size-discrimination studies were performed. PBDE-209 NH2-MIL-125(Ti) Pristine Xe lamp, >420 nm 300 [116] 1 Hyphen indicates that this value was not found in the original report. Later, in 2016, the same group reported the incorporation of perylene-diimide (PDI) as photosensitizing linker to afford Zn-PDI MOF [57]. This material was employed as heterogeneous photocatalyst in photoreductive dehalogenation processes, C-H aromatic substitution reactions, oxidation of benzylic alcohols and oxidative coupling of amines. In 2018, García and collaborators [115] reported the synthesis and spectroscopic properties of Rudcbpy-UiO-67, which contains Ru IIbipyridine moieties. This MOF was employed in the photoreductive debromination of phenacyl bromide. In 2019, the same group presented the anchorage of subphtalocyanines as photoredox units to MIL-101(Cr)-NH2 through B-N interactions [71]. The SubPc@MIL-101(Cr)-NH2 MOF was employed in the in-situ generation of phenacyl radical (from phenacyl bromide) coupled to the alkylation of styrene. Finally, very recently, Ma, Zhao, and coworkers [116] reported the application of NH2-MIL-125(Ti) as heterogeneous photocatalyst for the reductive debromination of decabromodiphenylether (PBDE-209) and studied the dependence of this reaction on the nature of the hole-scavenger employed. The best results were obtained when triethanolamine was used. Xe lamp, Later, in 2016, the same group reported the incorporation of perylene-diimide (PDI) as photosensitizing linker to afford Zn-PDI MOF [57]. This material was employed as heterogeneous photocatalyst in photoreductive dehalogenation processes, C-H aromatic substitution reactions, oxidation of benzylic alcohols and oxidative coupling of amines.

Dehalogenation reactions mediated by MOFs
In 2018, García and collaborators [115] reported the synthesis and spectroscopic properties of Rudcbpy-UiO-67, which contains Ru II -bipyridine moieties. This MOF was employed in the photoreductive debromination of phenacyl bromide. In 2019, the same group presented the anchorage of subphtalocyanines as photoredox units to MIL-101(Cr)-NH 2 through B-N interactions [71]. The SubPc@MIL-101(Cr)-NH 2 MOF was employed in the in-situ generation of phenacyl radical (from phenacyl bromide) coupled to the alkylation of styrene. Finally, very recently, Ma, Zhao, and coworkers [116] reported the application of NH 2 -MIL-125(Ti) as heterogeneous photocatalyst for the reductive debromination of decabromodiphenylether (PBDE-209) and studied the dependence of this reaction on the nature of the hole-scavenger employed. The best results were obtained when triethanolamine was used.
Dehalogenation reactions mediated by COFs (Table 15): In the field of COFs, three very recent contributions can be found in the literature. Two of them are devoted to the design of photoactive building blocks. On the one hand, Liu and collaborators [117] designed a benzothiadiazole-dialdehyde, able to condensate with a tetratopic-planar amine into a bidimensional imine-based COF, JLU-22. This COF was employed as photocatalyst for both photoreductive debromination and α-alkylation of aldehydes, using different phenacyl bromides and bromomalonates as starting materials. On the other hand, as previously explained in CDC section, two bidimensional imine-based COFs that contain triphenylamine and tetraphenylethylene units as photosensitizers were synthesized by Cui and coworkers [67] (Figure 17). They present high photoredox activity for debromination and CDC reactions. They performed the asymmetric α-alkylation of aldehydes using a chiral imidazolidinone as organocatalyst and 2,6-lutidine as additive. As starting materials, different bromomalonates and sterically hindered aliphatic aldehydes were used, obtaining from moderate-to-good yields and excellent enantioselectivities. Finally, our group presented the covalent incorporation of photocatalytically active Pt II -hydroxyquinoline complexes into an imine-based layered COF through monomer truncation strategy. Pt@COF is able to act both as an energy transfer and electron transfer photocatalyst, presenting very high turnover numbers (>8000 TON) towards sulfoxidation and photoreductive dehalogenation reactions. In particular, different malonate, benzylic, phenacyl, and aromatic bromides were efficiently reduced to the corresponding products under mild and green conditions [72]. 1 Hyphen indicates that this value was not found in the original report.
Catalysts 2020, 10, x FOR PEER REVIEW 30 of 44 materials. On the other hand, as previously explained in CDC section, two bidimensional iminebased COFs that contain triphenylamine and tetraphenylethylene units as photosensitizers were synthesized by Cui and coworkers [67] ( Figure 17). They present high photoredox activity for debromination and CDC reactions. They performed the asymmetric α-alkylation of aldehydes using a chiral imidazolidinone as organocatalyst and 2,6-lutidine as additive. As starting materials, different bromomalonates and sterically hindered aliphatic aldehydes were used, obtaining from moderate-to-good yields and excellent enantioselectivities. Finally, our group presented the covalent incorporation of photocatalytically active Pt II -hydroxyquinoline complexes into an imine-based layered COF through monomer truncation strategy. Pt@COF is able to act both as an energy transfer and electron transfer photocatalyst, presenting very high turnover numbers (>8000 TON) towards sulfoxidation and photoreductive dehalogenation reactions. In particular, different malonate, benzylic, phenacyl, and aromatic bromides were efficiently reduced to the corresponding products under mild and green conditions [72].  1 Hyphen indicates that this value was not found in the original report.

Other Reactions
Apart from oxidation processes, oxidative couplings, cross-dehydrogenative couplings, and dehalogenation reactions, some other organic transformations have been tested in order to evaluate and probe the photocatalytic activity of MOFs and COFs.
In the field of MOFs (Table 16), the three strategies presented in Section 2 have been applied in different reactions. For example, in 2018, Duan and coworkers [49] designed different linkers containing triphenylamine and thiophene moieties in order to synthesize the pristine Zn-BTCA MOF. This MOF presented high photocatalytic activity in a sulfonylation-cyclization tandem reaction of N-arylmethacrylamides and N-aroxyl-methacrylamides (Scheme 12), leading to the formation of the corresponding arylsulfonyl isoquinolinediones or oxindoles. Amine-alcohol condensation PdAu@MIL-100(Fe) Hybrid Xe lamp 420-800 nm 300 [78] 1 Hyphen indicates that this value was not found in the original report. Another pristine photocatalytic MOF was obtained by Xing and collaborators [46], containing anthracene units. This material ([Zn3(OH)2(ADBEB)2]•3DEF) was capable of performing not only the synthesis of imine compounds through oxidative reactions, but also reductive processes, such as the reduction of nitrophenols to the corresponding anilines, using EtOH and hydrazine hydrate as solvents. In the same year, Cheng, Zhang, and coworkers [34] synthesize Ru(bpy)3@NKMOFs by an in situ construction of the corresponding ZIF in presence of Ru(bpy)3. The occluded complex was capable of catalyzing oxidation of organic bromides to the corresponding carbonylic compounds (see above), and also the cyclization reaction between tertiary anilines and maleimides, affording the synthesis of ring-fused tetrahydroquinolines (Scheme 13).

Scheme 13. Photocyclization reaction between tertiary anilines and maleimides.
Post-functionalized MOFs played a key role in some examples of photocatalyzed organic transformations. In 2016, UiO-67 was post-functionalized with two organometallic Ir complexes by Cohen and Yu [118]. The two UiO-67-Ir MOFs were tested in the trifluoroethylation of styrene, observing a change of selectivity from the homogenously catalyzed reaction to the heterogeneous version (Scheme 14). When Ir-phenylpyridine homogenous complexes were tested, although full conversion was obtained, the major product was a dimeric species. However, when the complexes were immobilized and isolated into the porous framework, the reaction proceeded towards the mono-hydroxy-trifluoroethylated product. In addition, this change of selectivity was observed for 5 different substrates. Another pristine photocatalytic MOF was obtained by Xing and collaborators [46], containing anthracene units. This material ([Zn 3 (OH) 2 (ADBEB) 2 ]·3DEF) was capable of performing not only the synthesis of imine compounds through oxidative reactions, but also reductive processes, such as the reduction of nitrophenols to the corresponding anilines, using EtOH and hydrazine hydrate as solvents. In the same year, Cheng, Zhang, and coworkers [34] synthesize Ru(bpy) 3 @NKMOFs by an in situ construction of the corresponding ZIF in presence of Ru(bpy) 3 . The occluded complex was capable of catalyzing oxidation of organic bromides to the corresponding carbonylic compounds (see above), and also the cyclization reaction between tertiary anilines and maleimides, affording the synthesis of ring-fused tetrahydroquinolines (Scheme 13). Another pristine photocatalytic MOF was obtained by Xing and collaborators [46], containing anthracene units. This material ([Zn3(OH)2(ADBEB)2]•3DEF) was capable of performing not only the synthesis of imine compounds through oxidative reactions, but also reductive processes, such as the reduction of nitrophenols to the corresponding anilines, using EtOH and hydrazine hydrate as solvents. In the same year, Cheng, Zhang, and coworkers [34] synthesize Ru(bpy)3@NKMOFs by an in situ construction of the corresponding ZIF in presence of Ru(bpy)3. The occluded complex was capable of catalyzing oxidation of organic bromides to the corresponding carbonylic compounds (see above), and also the cyclization reaction between tertiary anilines and maleimides, affording the synthesis of ring-fused tetrahydroquinolines (Scheme 13).

Scheme 13. Photocyclization reaction between tertiary anilines and maleimides.
Post-functionalized MOFs played a key role in some examples of photocatalyzed organic transformations. In 2016, UiO-67 was post-functionalized with two organometallic Ir complexes by Cohen and Yu [118]. The two UiO-67-Ir MOFs were tested in the trifluoroethylation of styrene, observing a change of selectivity from the homogenously catalyzed reaction to the heterogeneous version (Scheme 14). When Ir-phenylpyridine homogenous complexes were tested, although full conversion was obtained, the major product was a dimeric species. However, when the complexes were immobilized and isolated into the porous framework, the reaction proceeded towards the mono-hydroxy-trifluoroethylated product. In addition, this change of selectivity was observed for 5 different substrates.

Scheme 13. Photocyclization reaction between tertiary anilines and maleimides.
Post-functionalized MOFs played a key role in some examples of photocatalyzed organic transformations. In 2016, UiO-67 was post-functionalized with two organometallic Ir complexes by Cohen and Yu [118]. The two UiO-67-Ir MOFs were tested in the trifluoroethylation of styrene, observing a change of selectivity from the homogenously catalyzed reaction to the heterogeneous version (Scheme 14). When Ir-phenylpyridine homogenous complexes were tested, although full conversion was obtained, the major product was a dimeric species. However, when the complexes were immobilized and isolated into the porous framework, the reaction proceeded towards the mono-hydroxy-trifluoroethylated product. In addition, this change of selectivity was observed for 5 different substrates. observing a change of selectivity from the homogenously catalyzed reaction to the heterogeneous version (Scheme 14). When Ir-phenylpyridine homogenous complexes were tested, although full conversion was obtained, the major product was a dimeric species. However, when the complexes were immobilized and isolated into the porous framework, the reaction proceeded towards the mono-hydroxy-trifluoroethylated product. In addition, this change of selectivity was observed for 5 different substrates.  Finally, some examples of hybrid MOFs can be found. For example, Duan and collaborators [48] synthesized the hybrid DT-BPY, which is formed by the combination of a photoactive decatungstate and a Cu-MOF, in order to perform the selective C-H alkylation of aliphatic nitriles under a high-power lamp (Scheme 16). In 2018, Li and coworkers [79] impregnated NH 2 -UiO-66(Zr) with Pd and Cu centers, that became Cu-Pd nanoclusters after a reductive treatment with NaBH 4 . The resulting hybrid CuPd@NH 2 -UiO-66(Zr) presented high photocatalytic activity and selectivity in light-induced Suzuki cross-coupling reactions between aryliodides and arylboronic acids, avoiding homocoupling unproductive pathways. The same group applied the mentioned strategy in obtaining PdAu@MIL-100(Fe), that is photocatalytically active in the tandem N-alkylation of amines with alcohols [78]. Finally, some examples of hybrid MOFs can be found. For example, Duan and collaborators [48] synthesized the hybrid DT-BPY, which is formed by the combination of a photoactive decatungstate and a Cu-MOF, in order to perform the selective C-H alkylation of aliphatic nitriles under a highpower lamp (Scheme 16). In 2018, Li and coworkers [79] impregnated NH2-UiO-66(Zr) with Pd and Cu centers, that became Cu-Pd nanoclusters after a reductive treatment with NaBH4. The resulting hybrid CuPd@NH2-UiO-66(Zr) presented high photocatalytic activity and selectivity in lightinduced Suzuki cross-coupling reactions between aryliodides and arylboronic acids, avoiding homocoupling unproductive pathways. The same group applied the mentioned strategy in obtaining PdAu@MIL-100(Fe), that is photocatalytically active in the tandem N-alkylation of amines with alcohols [78].  In the field of COFs (Table 17), many contributions in other organic transformations can be found, related to the employ of pristine materials. The first example where COFs were used as photocatalysts is from 2016, when Zhang and collaborators [120] designed a CTF containing benzothiadiazole moieties through cyclotrimerization of nitriles, using SiO 2 -NPs as template for the material growth. This nanostructured CTF was employed as catalyst in the photoreduction of nitrophenol to aminophenol under green conditions. Two asymmetric CTFs were synthesized in 2018 by the same group, containing thiophene units. CTF-Th and CTF-Th-Ph were used for the photocatalytic synthesis of benzophosphole oxides, in presence of an external oxidant (Scheme 17) [121].
Catalysts 2020, 10, x FOR PEER REVIEW 33 of 44 material growth. This nanostructured CTF was employed as catalyst in the photoreduction of nitrophenol to aminophenol under green conditions. Two asymmetric CTFs were synthesized in 2018 by the same group, containing thiophene units. CTF-Th and CTF-Th-Ph were used for the photocatalytic synthesis of benzophosphole oxides, in presence of an external oxidant (Scheme 17) [121]. In 2019 and 2020, Yang's group [122][123][124] employed 2D-COF-1, an acylhydrazone-based COF, as photocatalytic pristine material in three different organic transformations: radical additioncyclization of 2-arylphenylisocyanides [122], C3-arylation of quinoxalinones [123] and synthesis of 1,2,4-thiadiazoles [124] (Scheme 18). In the three cases, the catalyst was recycled up to 5 times without losing its photocatalytic activity under environmentally friendly conditions. In 2019, an interesting application of a pristine β-ketoenamine-based COF (TpTt) for the photoisomerization of double C-C bonds was reported by Banerjee and collaborators [25]. The TpTt-COF, formed by the condensation of the readily accessible melamine and triformylphloroglucinol, was employed in order to isomerize a variety of substituted olefins from trans to cis configuration under visible light irradiation. Parallelly, Thomas and coworkers constructed donor-acceptor iminebased COFs containing triazine and thiophene/dithiophene units (TTT-DTDA and TTT-BTDA) as heterogeneous photosensitizers for radical polymerization processes under visible light irradiation [125]. Very recently, Li, Zhao and collaborators synthesized fully conjugated COFs through postthermal treatment of imine-based COFs containing thiophene moieties. These materials were employed for the photoregeneration of NADH under visible light irradiation [24].
Apart from pristine COFs, only one example of hybrid material has been studied for other photocatalytic organic transformations by Kim and collaborators in 2018 [126]. In this work, they constructed COF-LZU-1 (an imine-based COF) over TiATA-MOF (which contains amino moieties), and then a Pd source was added to the hybrid. After the reduction of Pd centers, the multicomponent material Pd/TiATA@LZU1 was used for the selective photoreduction of styrene under visible light irradiation. The catalyst was recycled up to 8 times without losing its photocatalytic activity. In 2019 and 2020, Yang's group [122][123][124] employed 2D-COF-1, an acylhydrazone-based COF, as photocatalytic pristine material in three different organic transformations: radical addition-cyclization of 2-arylphenylisocyanides [122], C3-arylation of quinoxalinones [123] and synthesis of 1,2,4-thiadiazoles [124] (Scheme 18). In the three cases, the catalyst was recycled up to 5 times without losing its photocatalytic activity under environmentally friendly conditions. Catalysts 2020, 10, x FOR PEER REVIEW 33 of 44 material growth. This nanostructured CTF was employed as catalyst in the photoreduction of nitrophenol to aminophenol under green conditions. Two asymmetric CTFs were synthesized in 2018 by the same group, containing thiophene units. CTF-Th and CTF-Th-Ph were used for the photocatalytic synthesis of benzophosphole oxides, in presence of an external oxidant (Scheme 17) [121]. In 2019 and 2020, Yang's group [122][123][124] employed 2D-COF-1, an acylhydrazone-based COF, as photocatalytic pristine material in three different organic transformations: radical additioncyclization of 2-arylphenylisocyanides [122], C3-arylation of quinoxalinones [123] and synthesis of 1,2,4-thiadiazoles [124] (Scheme 18). In the three cases, the catalyst was recycled up to 5 times without losing its photocatalytic activity under environmentally friendly conditions. In 2019, an interesting application of a pristine β-ketoenamine-based COF (TpTt) for the photoisomerization of double C-C bonds was reported by Banerjee and collaborators [25]. The TpTt-COF, formed by the condensation of the readily accessible melamine and triformylphloroglucinol, was employed in order to isomerize a variety of substituted olefins from trans to cis configuration under visible light irradiation. Parallelly, Thomas and coworkers constructed donor-acceptor iminebased COFs containing triazine and thiophene/dithiophene units (TTT-DTDA and TTT-BTDA) as heterogeneous photosensitizers for radical polymerization processes under visible light irradiation [125]. Very recently, Li, Zhao and collaborators synthesized fully conjugated COFs through postthermal treatment of imine-based COFs containing thiophene moieties. These materials were employed for the photoregeneration of NADH under visible light irradiation [24].
Apart from pristine COFs, only one example of hybrid material has been studied for other photocatalytic organic transformations by Kim and collaborators in 2018 [126]. In this work, they constructed COF-LZU-1 (an imine-based COF) over TiATA-MOF (which contains amino moieties), and then a Pd source was added to the hybrid. After the reduction of Pd centers, the multicomponent material Pd/TiATA@LZU1 was used for the selective photoreduction of styrene under visible light irradiation. The catalyst was recycled up to 8 times without losing its photocatalytic activity. In 2019, an interesting application of a pristine β-ketoenamine-based COF (TpTt) for the photoisomerization of double C-C bonds was reported by Banerjee and collaborators [25]. The TpTt-COF, formed by the condensation of the readily accessible melamine and triformylphloroglucinol, was employed in order to isomerize a variety of substituted olefins from trans to cis configuration under visible light irradiation. Parallelly, Thomas and coworkers constructed donor-acceptor imine-based COFs containing triazine and thiophene/dithiophene units (TTT-DTDA and TTT-BTDA) as heterogeneous photosensitizers for radical polymerization processes under visible light irradiation [125]. Very recently, Li, Zhao and collaborators synthesized fully conjugated COFs through post-thermal treatment of imine-based COFs containing thiophene moieties. These materials were employed for the photoregeneration of NADH under visible light irradiation [24].
Apart from pristine COFs, only one example of hybrid material has been studied for other photocatalytic organic transformations by Kim and collaborators in 2018 [126]. In this work, they constructed COF-LZU-1 (an imine-based COF) over TiATA-MOF (which contains amino moieties), and then a Pd source was added to the hybrid. After the reduction of Pd centers, the multicomponent material Pd/TiATA@LZU1 was used for the selective photoreduction of styrene under visible light irradiation. The catalyst was recycled up to 8 times without losing its photocatalytic activity. 1 Hyphen indicates that this value was not found in the original report.

Comparative Critical Discussion on the Use of MOFs and COFs in Photocatalytic Organic Transformations
Up to this point, all available data in literature reporting the use of MOFs and COFs on photocatalytic organic transformations have been systematically presented in this review. This last section is intended to offer a brief comparative overview about the inherent features of one and another family of materials.
A detailed analysis of the presented examples revealed different tendencies on the use of both MOFs and COFs. First, it is worth to mention that the first report where MOFs were synthesized and characterized was published in 1999 [1]. Few years later, the first COF was published in 2005 [2]. Even though COFs have been object of study for fifteen years now, the quantity of works devoted to this family of materials is significantly lower than the studies invested in the use of MOFs. Although the time span between the invention of MOFs and the discovery of COFs could be one reason for the different attention that attracted both kind of materials, also it should be taken into account that crystalline MOFs (even single crystals) are easier to obtain. Therefore, the feasibility of structural insights on MOFs boosted the exploration of many applications of these materials. Consequently, applications of COFs are still underrepresented in the current literature in comparison with their metal-organic analogues. In particular, some distinct strategies have been used in the design of both photocatalytically active MOFs and COFs. While pristine MOFs represent the 60% of examples of photocatalytic synthetic applications, for COFs, this contribution reaches 90%. In addition, they differ in the applied sub-strategy (see Section 2.1 for further details): as far as MOFs are concerned, the design of intrinsically photoactive linkers is the dominant procedure, while for COFs, the use of imine-, β-ketoenamine-, hydrazone-or cyanovinylene-based undecorated materials is preferred. This difference can be attributed to the enhanced electronic delocalization that occurs in highly conjugated COFs but resulting difficult on MOFs, because of the presence of metal centers in a variety of coordination environments. Thus, the difficult conjugation and electron delocalization observed for MOFs, make necessary the predesign and introduction of photoactive linkers into the material backbone. Otherwise, functionalization protocols or obtaining hybrid photoactive materials have been extensively studied in MOFs but remains scarcely explored for COFs. In fact, the major part of examples found for functionalized or hybrid COFs are devoted to HER or carbon dioxide photoreduction, which are not part of this review [18]. In contrast, although some examples of MOF-hybrid materials are also applied to HER [127] and CO 2 photoreduction [128], many examples of photocatalytic applications of such kind of materials can be found. Among them, the selective oxidation of aromatic alcohols is the one that attracted more attention.
In this review, we considered four main photocatalytic organic transformations: oxidation, oxidative coupling, cross-dehydrogenative coupling, and dehalogenation reactions. These reactions imply that 85% of all the photocatalytic organic transformations are mediated by MOFs. However, this group of transformations only represent 70% of the photocatalytic organic processes catalyzed by COFs. This observation is suggesting that COFs seem to be more versatile as photocatalytic platforms for organic transformations. It can be attributed to the possibility of design and modulation of the photophysical properties of organic frameworks.
In this review, catalytic materials have been classified into three different synthetic strategies: pristine, functionalized, and hybrid materials. Each of them has its advantages and disadvantages. For example, the use of pristine materials requires a careful design of the building blocks taking into account length and orientations. In contrast, pristine materials have generally the advantage of obtaining homogeneous materials, being the porosity and pore size easily controllable. On the other hand, post-functionalized materials generally do not require such an exhaustive design of the building blocks, allowing easier synthetic procedures. However, the post-functionalization process makes it difficult to control the following factors: (1) the catalytic loading, (2) the homogeneity of the material, and (3) the porosity and pore size. Finally, hybrid materials make possible the combination of very diverse properties, which gives rise to synergistic phenomena. However, it is difficult to find the appropriate strategy to avoid the segregation of the different components. Furthermore, the interaction at the interfaces does not always allow interplay between materials of different nature.
Light source: Another important subject to discuss is the different type of employed light source. In photochemistry, light is crucial, since it brings with it the essential energy to excite the photocatalyst into its excited state, generating the corresponding charge separation. Thus, it is mandatory to control the power of the light source, as well as its energy. On the one hand, high-power lamps can lead to decomposition processes, such as photobleaching of the material [129]. On the other hand, the use of high energy sources (UV lamps) can lead to background or side reactions. These factors must be considered, taking into account that several examples presented in this review use high energy or high-power light sources, which can account for undesired side reactions or uncatalyzed background pathways. For example, results found in our laboratory demonstrated that in dehalogenation reactions high power and/or UV lamps can lead to the scission of C-Br or C-I bonds in the absence of photocatalyst. Therefore, background processes should always be considered and substrates that do not show background pathways (under specific reaction conditions) must be employed. In addition, it is important to adequate the wavelength of the employed radiation to the band gap of the corresponding heterogeneous photocatalyst, in order to maximize the photon transfer and to minimize the loss of energy [17]. In such a way, the use of visible light LEDs seems to be the best option, since they allow the exhaustive control over the wavelength and they present low power energy [62,72]. The design of materials with two-photon absorption capability results are quite interesting, inasmuch as low energies (such as red light or even infrared irradiation) are useful for these type of systems [28,33]. As an alternative, the use of UV-Visible Xe or Hg lamps equipped with cut-off filters frequently appears in some of the examples presented herein [75]. However, the major part of the energy of these irradiation systems is lost in the filter, so the overall conversion of light energy into the chemical transformation is scarce. Therefore, sunlight or more efficient LEDs should be used in future studies.
Catalyst loading: Catalyst loading or reaction scale are parameters that widely change from one example to another of those presented in this review. The different conditions found in the literature can account for different factors, such as the dispersibility of the material, the opacity of the system, the concentration of the solution or the nature of the light source. It is evident that low catalyst loadings are desired, since they allow to obtain high turnover numbers, and the opacity of the system is significantly decreased, which oppositely increase the efficiency of the photon absorption by the photocatalyst. In some reported cases, the catalyst loading implies the use of similar weights of photocatalytic material and reagents. Even though this does not seem to be an economically efficient strategy, the ratio between the moles of substrates transformed and the number of catalytically active sites is not obvious. This is because in many cases not all the material is equally active, being the surface the main responsible of the photocatalytic activity. Otherwise, scalability of heterogeneous photochemistry is quite difficult. In all the related examples, the scale is maintained below to 3 mmol scale [78], which is far from the requirements of fine chemicals industry. Resorting to flow photochemistry is therefore a remaining challenge on this field.
Solvent: The election of the solvent can also drastically change the catalytic outcome of the photocatalyzed reactions and their further applications. This is because some factors, such as suspension and stability of the heterogeneous photocatalyst, the solubility of the reagents and products and the photophysical properties of the solvated catalyst and substrates, can have a significant effect on the photocatalytic outcome. In addition, non-toxic solvents such as water are the most desired ones, which could fulfill the requirements of green chemistry. However, not all heterogeneous catalysts are stable enough against hydrolysis processes. For example, a variety of MOFs and boroxineor boronate-based COFs are readily disassembled in aqueous media, limiting their applications. Thus, some strategies have been developed in order to obtain hydrolysis-stable MOFs, such as the use of high-valent metal-containing MOFs with O-enriched linkers or low-valent metal-containing MOFs with N-enriched linkers, as well as the employ of hydrophobic ligands or post-synthetic modification protocols [130]. Otherwise, the development of different hydrolysis-stable types of linkages (see Section 2 for further details) was the key on the field of COFs. Due to the characteristics of MOF and COFs systems, in most cases polar organic solvents such as acetonitrile, aliphatic alcohols or ethers are employed.
Stability/Integrity: A final factor that should be taken into account regarding the stability of photocatalytic materials is the possible chemical erosion triggered by its reactivity with the organic substrates. In particular, it has been observed that imine-based COFs are sensitive to nucleophilic attack of reagents, such as amines or malononitriles, as a consequence of the reversible nature of the imine bond [107]. This decomposition can compete with catalyzed reactions, that uses this kind of reagents (e.g., oxidative coupling of amines). Therefore, leaching and recyclability experiments should be performed in order to discard the disassembly of the material under the specific reaction conditions.

Concluding Remarks and Perspectives
The extensive overview of the available literature devoted to organic synthetic applications of photocatalytic systems based on COFs and MOFs demonstrates the versatility of these materials and their potential for further findings. From a structural point of view, strategies for the design of reticular materials, with a variety of geometries and topologies, has reached a high degree of maturity. As a consequence, some of the most common photocatalytic transformations reported for molecular systems have already been reported for reticular materials, and this review has carefully compiled the recent literature in this respect. However, considering the volume of work published and the complexity of processes and products reported, it seems that this field is still in its infancy. In fact, the MOFs/COFs scientific community has a clear bias towards the detailed structural elucidation and physical characterization of such reticular materials. However, the study of their catalytic (and in particular photocatalytic) applications are still very limited. As a consequence, apart from punctual cases, the typical mentioned transformations are currently studied as model systems, without exploring the full catalytic potential of many MOFs and COFs. Many challenges addressed on molecular systems remain clearly underexplored for photocatalytic MOFs or COFs, such as synthesis of asymmetric products or cooperative multicomponent catalysis. In addition, the particular advantages that could be specifically derived from the use of reticular materials have not been fully explored. In this sense, the examples of size discrimination phenomena or confinement effects are underrepresented in literature. Thus, further significant developments could be related to these aspects.
Interestingly, a comparable number of works have been found using MOFs and COFs for photocatalytic organic synthetic applications. This fact is somehow surprising considering that the number of MOFs reported is approximately two orders of magnitude higher than the number of COFs. Further work will be needed to determine if this observation is related to the different intrinsic nature of both kind of materials or is just the result of the different focus that the MOF and COF communities apply to their research. However, it is worth to note that the wide range of possibilities that COFs offer for the incorporation of predesigned organic fragments makes this kind of materials especially appealing for advanced photocatalytic applications.
From a methodological perspective, the examination of the literature available should serve to stablish some principles that would allow to ensure the significance of the results and the future benchmarking of the published data. Up to now, a series of factors have not been systematically considered, making difficult the comparison between different systems. Some of these factors are wavelength and power of light source, checking of uncatalyzed photochemical background reactions, evaluation of recyclability and leaching phenomena, or the relative catalytic loading (which in some cases is stoichiometric or even superstoichiometric). Systematic incorporation of discussions on these factors in future works would be extremely useful.
Overall, the body of data compiled in this review confirms that the state of the art of photocatalytic applications of COFs and MOFs for organic transformations allows the laying of foundations of future developments. Therefore, much research is expected in the next few years that could fully explore all the potential of reticular chemistry to address the challenges that modern chemistry has ahead in the fields of energy conversion, design of environmentally benign processes or the production of high added value products.

Conflicts of Interest:
The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.