Dendritic Macrosurfactant Assembly for Physical Functionalization of HIPE-Templated Polymers

High-internal-phase emulsion-templated macroporous polymers (polyHIPEs) have attracted much interest, but their surface functionalization remains a primary concern. Thus, competitive surface functionalization via physical self-assembly of macrosurfactants was reviewed. Dendritic and diblock-copolymer macrosurfactants were tested, and the former appeared to be more topologically competitive in terms of solubility, viscosity, and versatility. In particular, hyperbranched polyethyleneimine (PEI) was transformed into dendritic PEI macrosurfactants through click-like N-alkylation with epoxy compounds. Free-standing PEI macrosurfactants were used as molecular nanocapsules for charge-selective guest encapsulation and robustly dictated the surface of a macroporous polymer through the HIPE technique, in which the macroporous polymer could act as a well-recoverable adsorbent. Metal nanoparticle-loaded PEI macrosurfactants could similarly lead to polyHIPE, whose surface was dictated by its catalytic component. Unlike conventional Pickering stabilizer, PEI macrosurfactant-based metal nanocomposite resulted in open-cellular polyHIPE, rendering the catalytic sites well accessible. The active amino groups on the polyHIPE could also be transformed into functional groups of aminopolycarboxylic acids, which could efficiently eliminate trace and heavy metal species in water.


Introduction
Given the potential of high-internal-phase emulsion (HIPE)-templated macroporous polymers (polyHIPEs) in adsorption [1][2][3][4], catalysis [5][6][7][8], bioapplication [9], and separation [10] due to its invention [11], these polymers have been well reviewed by a number of researchers [12][13][14][15][16][17]. HIPE is defined as an emulsion whose internal phase makes up over 74% of the total system volume. HIPE can be prepared by either dispersing water in oil (W/O), oil in water (O/W), air in oil, or supercritical carbon dioxide in oil. Among these techniques, W/O emulsion is the most widely studied, partly because of easy access to green water. In the present study, HIPE was prepared via W/O unless stated otherwise. PolyHIPEs are widely explored due to their cost-effective preparation, relatively large specific surface area, interconnected pores, and wide range of potential applications. These applications are largely determined by their surface functions. Surface functionalization of polyHIPEs can be performed using intrinsic functional monomers, through chemical postmodification of the matrix, or using functional surfactants, where the last method is less explored. Small surfactants are not recommended for surface functionalization, because they can be readily washed away, but reactive surfactants cannot [18,19]. Surface functionalization of polyHIPE can be performed via self-assembly of macrosurfactants, especially of dendritic macrosurfactants, which are less studied and have not been

Synthesis of PEI Macrosurfactants
PEI contains dense primary, secondary, and tertiary amino groups ( Figure 1). Amino groups from small molecules are reactive and readily modified by chemical reactions, but PEIs are not. Upon encountering reactants such as fatty acid chlorides or fatty acid anhydrides, PEIs tend to immediately form precipitants in conventional media, where the reaction becomes inefficient, and tedious purification of the product is necessary. The insolubility typically results from salt formation in PEI. The degree of N-alkylation in PEI is also critical to its solubility. If the PEI core is sufficiently alkylated with apolar cetyl chains, the resulting macrosurfactant typically demonstrates good solubility in organic solvents. However, if limited cetyl chains are introduced to one PEI, the resulting product appears to be poorly soluble in either polar or apolar media, possibly because of the strong complementary interactions among the polar cores. Several methods, including well-defined ones [33], have been developed for the synthesis of PEI macrosurfactants [25][26][27][28][29][30][31][32][33][34]. The reaction between epoxy compounds and primary or secondary amino groups is mild, efficient, and does not release side products. When the epoxy-amine reaction is applied to PEI modification, quantitative PEI macrosurfactants with designed N-alkylation degrees can be obtained [33], even if the epoxy compound is a macromolecule [33]. PEI macrosurfactants have numerous residual active amines in the core (Figure 1).

PEI Macrosurfactants as Free Molecular Nanocapsules
PEI can be quantitatively alkylated with glycidyl cetyl (1a-1f, Figure 2), and up to 90% of the amino protons can be replaced with cetyl groups [33]. A high degree of N-alkylation leads to a high possibility of PEI macrosurfactants existing as free molecular nanocapsules [33]. Any of the PEI macrosurfactants in 1a-1f could undergo highly charge-selective guest encapsulation and be used for separating anionic-cationic organic mixtures. The multifunctional core could also be further engineered (1d-4d, Figure 2) for guest selectivity. Quaternization of the PEI core (4d) did not favor charge selectivity and even decreased it, which can be attributed to the van de Waals complement. Evidence showed that the guest selectivity in 1d-4d is related to H-bonding, dipolar-dipolar interactions, and dispersion forces with a guest molecule. For example, 2d showed higher affinity to methyl orange than 3d, because methyl orange is both anionic and largely apolar, which is preferred for complementing with less-polar 2d. Tailoring the core of a molecular nanocapsule can lead to fine differentiation of very similar guests of rose bengal/erythrosine B/eosin Y [35,36]. Deprotonation of PEI leads to the considerable release of encapsulated guests after increasing the pH level [32]. Moreover, molecular nanocapsules are durable and well pH-recyclable, because no acid-or base-labile bonds are present. Chen et al. [30] found that dendritic topology is critical to the guest encapsulation of dendritic molecular nanocapsules, because the linear counterpart cannot efficiently encapsulate similar guests. Alkylated PEI has charge-selective guest encapsulation. Figure 3 shows 100% separated anionic-cationic guests and that the encapsulated dye could be released by pH adjustment, as monitored with a Uv/vis spectrometer [32]. In case the dye is of small size, the encapsulation or releasing equilibration takes seconds to hours; if the dye is of large size, it takes days.

PEI Macrosurfactants as Free Molecular Nanocapsules
PEI can be quantitatively alkylated with glycidyl cetyl (1a-1f, Figure 2), and up to 90% of the amino protons can be replaced with cetyl groups [33]. A high degree of N-alkylation leads to a high possibility of PEI macrosurfactants existing as free molecular nanocapsules [33]. Any of the PEI macrosurfactants in 1a-1f could undergo highly charge-selective guest encapsulation and be used for separating anionic-cationic organic mixtures. The multifunctional core could also be further engineered (1d-4d, Figure 2) for guest selectivity. Quaternization of the PEI core (4d) did not favor charge selectivity and even decreased it, which can be attributed to the van de Waals complement. Evidence showed that the guest selectivity in 1d-4d is related to H-bonding, dipolar-dipolar interactions, and dispersion forces with a guest molecule. For example, 2d showed higher affinity to methyl orange than 3d, because methyl orange is both anionic and largely apolar, which is preferred for complementing with less-polar 2d. Tailoring the core of a molecular nanocapsule can lead to fine differentiation of very similar guests of rose bengal/erythrosine B/eosin Y [35,36]. Deprotonation of PEI leads to the considerable release of encapsulated guests after increasing the pH level [32]. Moreover, molecular nanocapsules are durable and well pH-recyclable, because no acid-or base-labile bonds are present. Chen et al. [30] found that dendritic topology is critical to the guest encapsulation of dendritic molecular nanocapsules, because the linear counterpart cannot efficiently encapsulate similar guests. Alkylated PEI has charge-selective guest encapsulation. Figure 3 shows 100% separated anionic-cationic guests and that the encapsulated dye could be released by pH adjustment, as monitored with a Uv/vis spectrometer [32]. In case the dye is of small size, the encapsulation or releasing equilibration takes seconds to hours; if the dye is of large size, it takes days.

Direct Dictation of PolyHIPE Surface with PEI Macrosurfactants
Chemical functionalization of a preformed inert polyHIPE is tedious and costly. Physical functionalization has been recently performed using HIPE. Ye et al. [3] directly prepared a functional polyHIPE with a polystyrene (PS)-alkylated PEI (PEI@PS) as macrosurfactant ( Figure 4). PEI@PS acted as a HIPE stabilizer and subsequently dictated the surface of the as-prepared polyHIPE. The PS of PEI@PS was responsible for adhering to the polyHIPE matrix, whereas the functional PEI was responsible for guest adsorption. PEI@PS carried no pH-labile bond, indicating that the polyHIPE is chemically durable and has good recyclability properties. Dendritic PEI@PS also showed lower viscosity than its linear counterpart, which is favorable for HIPE [2]. In addition, polyHIPE with a patchy surface was obtained when two kinds of dendritic macrosurfactants were simultaneously charged in a HIPE system [4]. The polyHIPE could simultaneously remove distinctly different guest species from water because of this patchy surface.

Direct Dictation of PolyHIPE Surface with PEI Macrosurfactants
Chemical functionalization of a preformed inert polyHIPE is tedious and costly. Physical functionalization has been recently performed using HIPE. Ye et al. [3] directly prepared a functional polyHIPE with a polystyrene (PS)-alkylated PEI (PEI@PS) as macrosurfactant (Figure 4). PEI@PS acted as a HIPE stabilizer and subsequently dictated the surface of the as-prepared polyHIPE. The PS of PEI@PS was responsible for adhering to the polyHIPE matrix, whereas the functional PEI was responsible for guest adsorption. PEI@PS carried no pH-labile bond, indicating that the polyHIPE is chemically durable and has good recyclability properties. Dendritic PEI@PS also showed lower viscosity than its linear counterpart, which is favorable for HIPE [2]. In addition, polyHIPE with a patchy surface was obtained when two kinds of dendritic macrosurfactants were simultaneously charged in a HIPE system [4]. The polyHIPE could simultaneously remove distinctly different guest species from water because of this patchy surface. PEI@PS had a much higher molecular weight than small or diblock copolymer surfactants and did not leave the matrix ( Figure 5). For quantitative understanding, one can refer to the dependence of the life span (L) of an assembly on the molecular weight (Mn) of its building blocks through the relationship L = e Mn [46]. Considering that PEI@PS has a Mn = 10 5 Dalton, which is much larger than that of a small surfactant (Mn = 10 2 Dalton) or a block copolymer (Mn = 10 4 Dalton), the stability of a dendritic macrosurfactant can be exponentially improved. This finding was supported by the results of experiments, which showed good recyclability and the absence of any deterioration in the corresponding adsorbents. PEI@PS had a much higher molecular weight than small or diblock copolymer surfactants and did not leave the matrix ( Figure 5). For quantitative understanding, one can refer to the dependence of the life span (L) of an assembly on the molecular weight (M n ) of its building blocks through the relationship L = e Mn [46]. Considering that PEI@PS has a M n = 10 5 Dalton, which is much larger than that of a small surfactant (M n = 10 2 Dalton) or a block copolymer (M n = 10 4 Dalton), the stability of a dendritic macrosurfactant can be exponentially improved. This finding was supported by the results of experiments, which showed good recyclability and the absence of any deterioration in the corresponding adsorbents.

PEI Macrosurfactant-Aided Metal Nanoparticle-Dictated PolyHIPE
PEI can act as a multiligand of noble metal nanoparticles, which are well-known catalysts. Ye et al. [5] adopted the PEI@PS-mediated HIPE process to prepare gold nanoparticle-dictated polyHIPE by charging gold ion species during the water phase. Upon polyHIPE formation, the gold ions were simultaneously reduced to gold nanoparticles, with PEI acting as the ligand and reducer ( Figure 6). Alternatively, PEI@PS was loaded with gold nanoparticles in advance, and the resulting product was used as HIPE surfactant to similarly prepare polyHIPE. In both cases, open-cellular polyHIPEs were obtained, and both showed good catalytic and recyclability properties. Liu et al. [6] found that if the polyHIPE matrix was made of flexible polymers rather than brittle PS, no chalky fragment would form during catalytic application, which favors the recovery of platinum nanoparticle-dictated catalytic materials. Wan et al. [7] showed that when trace and optimized amounts of thiol groups are covalently introduced onto PEI, highly durable platinum nanoparticles can be obtained, and the catalytic activity is only slightly reduced by the thiol groups.
The open-cellular structure of a polyHIPE is critical to the accessibility of the surface and the catalytic sites. PolyHIPEs mediated with small molecular surfactant generally yield an open-cellular macroporous polymer, but the mechanism remains unclear. Block copolymer and dendritic macrosurfactants also typically lead to open-cellular polyHIPEs. One study attributed the mechanism to volume contraction upon gel formation [47]. Other studies suggested the role of phase separation and vacuum induction [48]. Li et al. [49] suggested that pore formation is not related to vacuum and attributed it to the combination of volume contraction and surfactant migration upon gelation. Closed cellular polyHIPE is typically obtained when nanoparticles are used as the stabilizer of a HIPE system (called Pickering emulsion). Ye et al. [5] and Liu et al. [6] obtained gold (or platinum) nanoparticle-mediated polyHIPEs with an open-cellular structure (which is critical to accessing catalytic sites). The free PEI macrosurfactants in the system possibly played a critical role, because when minor small surfactants are present in a Pickering emulsion system, open-cellular rather than closed-cellular polyHIPE is obtained [50][51][52][53][54][55].

PEI Macrosurfactant-Aided Metal Nanoparticle-Dictated PolyHIPE
PEI can act as a multiligand of noble metal nanoparticles, which are well-known catalysts. Ye et al. [5] adopted the PEI@PS-mediated HIPE process to prepare gold nanoparticle-dictated polyHIPE by charging gold ion species during the water phase. Upon polyHIPE formation, the gold ions were simultaneously reduced to gold nanoparticles, with PEI acting as the ligand and reducer ( Figure 6). Alternatively, PEI@PS was loaded with gold nanoparticles in advance, and the resulting product was used as HIPE surfactant to similarly prepare polyHIPE. In both cases, open-cellular polyHIPEs were obtained, and both showed good catalytic and recyclability properties. Liu et al. [6] found that if the polyHIPE matrix was made of flexible polymers rather than brittle PS, no chalky fragment would form during catalytic application, which favors the recovery of platinum nanoparticle-dictated catalytic materials. Wan et al. [7] showed that when trace and optimized amounts of thiol groups are covalently introduced onto PEI, highly durable platinum nanoparticles can be obtained, and the catalytic activity is only slightly reduced by the thiol groups.
The open-cellular structure of a polyHIPE is critical to the accessibility of the surface and the catalytic sites. PolyHIPEs mediated with small molecular surfactant generally yield an open-cellular macroporous polymer, but the mechanism remains unclear. Block copolymer and dendritic macrosurfactants also typically lead to open-cellular polyHIPEs. One study attributed the mechanism to volume contraction upon gel formation [47]. Other studies suggested the role of phase separation and vacuum induction [48]. Li et al. [49] suggested that pore formation is not related to vacuum and attributed it to the combination of volume contraction and surfactant migration upon gelation. Closed cellular polyHIPE is typically obtained when nanoparticles are used as the stabilizer of a HIPE system (called Pickering emulsion). Ye et al. [5] and Liu et al. [6] obtained gold (or platinum) nanoparticle-mediated polyHIPEs with an open-cellular structure (which is critical to accessing catalytic sites). The free PEI macrosurfactants in the system possibly played a critical role, because when minor small surfactants are present in a Pickering emulsion system, open-cellular rather than closed-cellular polyHIPE is obtained [50][51][52][53][54][55].

PEI Macrosurfactant-Aided AminopolycarboxylicAcid-Dictated PolyHIPE for Metal Ion Adsorption
Aminopolycarboxy acids (APAs) are known for their extremely high affinity for a wide spectrum of toxic and cationic metal species. Ethylenediaminetetraacetic acid and diethylenetriaminepentaacetic acid are typical members of the APA family. Many researchers have tried to attach APAs on a supported porous matrix [56], mainly via solid-phase reactions. After dictation on the polyHIPE surface, the active amino groups of PEI macrosurfactants represent a useful engineering platform. Weng et al. [57] very recently developed a physically aided and one-pot HIPE process for APA-dictated polyHIPE (Figure 7). The self-assembly of PEI macrosurfactant stabilized the HIPE and rendered the active amino groups arrayed along the oil/water interface, thereby leading to their transformation into APAs. The resulting polyHIPE can eliminate various heavy metal species at trace amounts in water. This adsorbent has the advantages of cost-effective preparation, high durability, and good metal-eliminating ability. However, the

PEI Macrosurfactant-Aided AminopolycarboxylicAcid-Dictated PolyHIPE for Metal Ion Adsorption
Aminopolycarboxy acids (APAs) are known for their extremely high affinity for a wide spectrum of toxic and cationic metal species. Ethylenediaminetetraacetic acid and diethylenetriaminepentaacetic acid are typical members of the APA family. Many researchers have tried to attach APAs on a supported porous matrix [56], mainly via solid-phase reactions. After dictation on the polyHIPE surface, the active amino groups of PEI macrosurfactants represent a useful engineering platform. Weng et al. [57] very recently developed a physically aided and one-pot HIPE process for APA-dictated polyHIPE (Figure 7). The self-assembly of PEI macrosurfactant stabilized the HIPE and rendered the active amino groups arrayed along the oil/water interface, thereby leading to their transformation into APAs. The resulting polyHIPE can eliminate various heavy metal species at trace amounts in water. This adsorbent has the advantages of cost-effective preparation, high durability, and good metal-eliminating ability. However, the linear counterpart of dendritic PEI macrosurfactant cannot be applied to the same process due to its very poor solubility, which stems from intermolecular complementary interaction-induced aggregation.
In the case of dendritic macrosurfactants, the intramolecular complement is predominant because of its globular molecular topology. linear counterpart of dendritic PEI macrosurfactant cannot be applied to the same process due to its very poor solubility, which stems from intermolecular complementary interaction-induced aggregation. In the case of dendritic macrosurfactants, the intramolecular complement is predominant because of its globular molecular topology.

Conclusions and Outlook
Dendritic PEI macrosurfactants could dictate the surface of an in-situ-prepared open-cellular polyHIPE, a typical kind of macroporous polymer, by using a HIPE templating technique. The dendritic macrosurfactants showed lower viscosity and better solubility than their linear counterparts, indicating their enhanced performance in a HIPE process. They robustly attached to the polyHIPE matrix regardless of the physical adhesion nature. PolyHIPEs with surfaces dictated

Conclusions and Outlook
Dendritic PEI macrosurfactants could dictate the surface of an in-situ-prepared open-cellular polyHIPE, a typical kind of macroporous polymer, by using a HIPE templating technique. The dendritic macrosurfactants showed lower viscosity and better solubility than their linear counterparts, indicating their enhanced performance in a HIPE process. They robustly attached to the polyHIPE matrix regardless of the physical adhesion nature. PolyHIPEs with surfaces dictated by functional PEI macrosurfactants could act as a well-recyclable adsorbent. Catalytic metal nanoparticles could be facilely introduced onto the surface of a polyHIPE through the help of PEI macrosurfactants, thereby making these nanoparticles readily recyclable catalysts. With the residual active amino groups on the polyHIPE surface, the polyHIPE was transformed into aminopolycarboxylic acid, capable of eliminating various heavy metal species from water.
The application of most polyHIPEs is related to their open-cellular structure and surface functions when adsorption and catalysis are involved. In this respect, dendritic macrosurfactants generally lead to an open-cellular structure and a designable functional surface. Moreover, dendritic macrosurfactants demonstrate a good open-cellular structure after being partly loaded with metal nanoparticles. Most functional inorganic-organic nanocomposite particles are amphiphilic; they possibly could be similarly immobilized on a polyHIPE surface.

Conflicts of Interest:
The authors declare no conflict of interest.