Enzyme Initiated Radical Polymerizations

Biocatalysis is propagating into practically every area of organic chemistry, amongst them radical polymerizations. A review of the recent developments of this dynamic and quickly evolving area of research is presented together with a critical evaluation of its potential to yield novel polymers and/or environmentally more benign synthetic procedures OA-fund TU Delft


Introduction
Great aspirations have been put on biocatalysts to make the chemical industry environmentally more benign and sustainable [1][2][3].Indeed, more and more examples impressively demonstrate the potential of White Biotechnology to reduce resource consumption and waste generation [1,[4][5][6].However, most of the ‗landmark' examples deal with the synthesis of small, chiral molecules useful for pharmaceuticals etc. Traditionally, the wastes generated in this industry are enormous, leaving room for significant improvements [7].The global impact, however, is limited by the comparably low production volumes.
In contrast, polymers are bulk products produced in huge annual quantities.Here, though the saving potential might be lower due to highly optimized ‗traditional' production schemes, even comparably small improvements may have a dramatic global impact.Hence, it is not astonishing that biocatalysis is also enjoying growing interest in the field of polymers [8].One field that has expanded tremendously in the past two decades is the enzyme-initiated radical polymerization of aromatic and vinyl monomers [8][9][10][11][12].In this contribution, we summarize and critically evaluate the past and recent developments in this field also giving an outlook of the future perspectives.

Mechanism(s) of Enzyme Initiated Radical Polymerizations
Two enzyme classes dominate the field of biocatalytic radical polymerization: peroxidases (EC 1.11.1) and laccases (EC 1.10.3.2).Though quite different with respect to catalytic mechanism and active site structure, both enzyme classes predominantly catalyze hydrogen abstraction reactions yielding radical species to initiate the polymerization reaction.Other enzyme classes such as oxidases or lipoxygenases play only a minor role [13][14][15].

Peroxidase-Initiated Polymerizations
By far the most popular catalysts for the enzymatic initiation of radical polymerization (both of aromatic and vinyl monomers) are the so-called heme peroxidases.Particularly, the peroxidases from horseradish (HRP) and soybean (SBP) have been used most frequently.
These peroxidases contain protoporphyrin IX (heme, Figure 1) as prosthetic group with low-spin Fe III in the resting state [16,17].During the catalytic mechanism (Figure 2) the water ligand (intermediate 1) is substituted by hydrogen peroxide (or other organic hydroperoxides) resulting in a peroxo complex (intermediate 2).Upon heterolytic cleavage of the O-O bond the so-called compound I (Cpd-I) is formed.Cpd-I returns into the resting state by two individual hydrogen abstractions from the reducing substrates (In-H) resulting in the formation of two radical species (In• ) which then initiate the polymerization process.Overall, peroxidases function as ‗electron relays' coupling a two electron transfer step (reduction of peroxides to water or alcohols, respectively) to two subsequent single electron transfer steps.
H 2 O 2 plays an ambivalent role in the peroxidase-initiated polymerization reaction.On the one hand, it serves as oxidant and therefore is essential for the catalytic action.On the other hand, if [H 2 O 2 ] is too high, polymerization is inhibited twofold: (1) H 2 O 2 is a known inactivator of heme [18,19].It was proposed that in the presence of an excess of H 2 O 2 Cpd-II reacts with another equivalent of H 2 O 2 instead of returning to the resting state.The resulting Cpd-III decomposes along various pathways leading to irreversible enzyme inactivation [19].(2) A catalase-like activity of peroxidases [20] at high [H 2 O 2 ] results in the generation of O 2 thereby inhibiting the chemical polymerization reaction.This effect has been reported especially for the polymerization of vinyl monomers in form of a lag-phase.During this lag phase, remaining O 2 is consumed, probably by reaction with In.The resulting superoxide anion (O 2

• −
) disproportionates quickly thereby overall accounting for a futile consumption of H 2 O 2 and radical quenching.It should, however, be emphasized that the exact mechanism remains to be elucidated.Polymerization only proceeds if O 2 formed by the catalase-activity has been consumed [21].

Figure 2.
Simplified catalytic mechanism of peroxidase-catalyzed radical formation.In the majority of cases L is a histidine ligand but can also be cysteine.
The usual way of avoiding excess H 2 O 2 is to add H 2 O 2 in several portions, which turns out to be tedious and also bears the danger of leading to a certain degree of irreproducibility.Therefore, a range of in situ H 2 O 2 generation methods have been proposed, [22][23][24] which might be useful also for peroxidase-initiated polymerizations.Indeed Uyama et al. and others reported a bienzymatic system for the polymerization of phenols comprising peroxidase as the initiation catalyst and glucose oxidase as in situ H 2 O 2 generation catalyst (Figure 3) [25,26].Interestingly, this system, despite its simplicity, has not found broad proliferation.Possibly, inhibitory effects of O 2 are quite severe in practice.
A rather unusual in situ generation of peroxo species was found accidentally by Samuelson and coworkers [27].They found that a dioxane stabilizer (acetyl acetal) spontaneously hydrolyzed under the reaction conditions and was oxidized to peracetic acid, which then served as oxidant to initiate the polymerization of aniline (Figure 4).Nevertheless, portionwise addition of H 2 O 2 remains the most popular procedure to promote peroxidase-initiated polymerizations.

Laccase-Initiated Polymerization
Laccases (E.C. 1.10.3.2) belong to the so-called blue-copper oxidases predominantly found in fungi but also in plants and insects [28][29][30][31].Laccases catalyze hydrogen abstraction reactions from phenolic and related substrates resulting in corresponding phenoxy radicals.They contain four copper ions classified in one T1 copper ion and a T2/T3 cluster.It has been shown that the T1 site is the primary redox center accepting electrons from the electron donors.Thus, the fully oxidized laccase is transformed via four successive, fast single electron transfer (SET) steps into the fully reduced laccase.Molecular oxygen interacts with the fully reduced (T2/T3) cluster via a fast 2-electron-transfer process.The resulting peroxide is tightly bound so that release of H 2 O 2 prior to the second 2-electron-transfer is efficiently prevented.As a result, the fully oxidized form of laccases comprising a μ 3 -oxo-bridged trinuclear (T2/T3) site is formed.This structure is thermodynamically relatively stable and provides the driving force for the overall process and also provides an efficient electron transfer bridge to re-generate the fully reduced state (Figure 5).
Interestingly enough, the number of publications dealing with laccase-initiated polymerization falls back significantly behind peroxidase-initiated polymerization studies.This is astonishing insofar as the laccase-based systems appear to be significantly easier.One apparent advantage is that laccases utilize molecular oxygen instead of hydrogen peroxide as oxidant, but inhibition may prevent widespread use.

Laccase-/Peroxidase-Mediator-Systems (LMS/PMS)
Often direct oxidation of the monomers is not possible due to unfavorable steric interaction with the enzymes' active sites and/or due to unfavorable redox potentials.In such cases, initiation of the polymerization reaction may take place by so-called laccase-or peroxidase mediator systems (LMS or PMS, respectively).Here, enzymatic chain initiation does not proceed directly on a monomer molecule but indirectly via a small, oxidizable mediator (Figure 6).Two mechanisms can be distinguished: First, the mediator can serve as radical transfer catalyst without being incorporated into the final product.Phenothiazenes, for example, have been used to initiate the polymerization of sterically demanding phenols, [32,33] or ABTS to facilitate pyrrole polymerization [34,35].Also transition metals (e.g., Mn 2+/3+ ) [36] or polyoxometallates [37] have been reported.Second, the mediator radical itself can initiate chain growth thereby being incorporated into the polymer (see Section 2.4).This mechanism is the predominant pathway for the polymerization of vinyl monomers with β-diketones representing the mediators of choice (vide infra) but may also be applicable for the polymerization of non-phenolic aromatics such as thiophenes [38].Figure 6.Schematic representation of laccase mediator systems (LMSs) and peroxidase mediator systems (PMSs) initiated polymerization reactions.Upper: the mediator is used as true catalyst transferring the radical to a monomer; Lower: the oxidized mediator radical itself initiates the polymerization process and hence is incorporated into the polymer.

Other Enzyme Systems/Miscellaneous
Very recently the groups around Bruns [39] and di Lena [40,41] independently reported on biocatalytic atom transfer radical polymerizations.
Using laccases or heme-enzymes such as catalase of HRP, an ATRP-like polymerization was achieved with ascorbic acid as reductant and α-bromoesters as initiators.Despite the very early stage of development (particularly further mechanistic studies clarifying the initiation reaction are needed), this approach represents already now a very promising biocatalytic alternative to the existing toolbox [42].Exciting further developments are expected here in the near future.Noteworthy, this approach also represents the first example(s) of a reductively initiated radical polymerization.
Ximenes and coworkers reported on the H 2 O 2 -independent Acac oxidation by HRP in the presence of molecular oxygen [43].Intermediate formation of Acac .and superoxide was postulated, which might potentially be exploited for the initiation of radical polymerizations.If feasible, such a pathway might open up new possibilities while circumventing the limitations of H 2 O 2 -promoted chain initiation reactions mentioned above.It remains to be shown whether such a mechanism might be fruitfully exploited for peroxidase-initiated polymerization reactions.

Controlling the Structure of the Polymers
Unlike most enzymatic transformations, oxidoreductase-initiated radical polymerizations lack any influence of the biocatalyst on the structure of the final product.Hence, if control over the structure and morphology of the polymer formed is desired, this has to be achieved with a mechanism which does not directly involve the enzyme.In the following some of the strategies generally applied are discussed.

Controlling Vinyl Polymerization
The major concern in vinyl polymerization is to control the polymer weight and polydispersity of the final product.In this respect, most studies have focused on the influence of biocatalyst-, mediator-, and oxidant concentration.
The biocatalyst concentration directly correlates with the chain initiation rate and thereby influences the number of growing chains in the reaction mixture and competing for the remaining monomers.As a rule of thumb, the higher the biocatalyst concentration the lower the average polymer weight, as demonstrated for peroxidases [44] and laccases [45].At very high enzyme concentration, the initiation rate can be so dominant that only oligomers are formed.Under denaturizing conditions, too low enzyme concentrations manifest in low conversions due to enzyme inactivation [46].
Like enzyme concentration, choice and concentration of the mediator can have a major impact on the polymer properties.This was demonstrated by Kaplan and coworkers on the HRP-initiated polymerization of styrene and by Marechal and coworkers for the polymerization of acrylamide (Table 1) [47,48].So far, detailed studies clarifying the influence of ß-diketone structure on enzyme activity are missing.Most likely, both steric and electronic effects influence the rate of the enzymatic initiation reaction as well as the rate of the chain growth (at least at an early stage of the chain growth).
It is generally assumed that the enol form represents the actual substrate for the enzymatic radical formation reaction (Figure 7) [49].The state of the keto-enol equilibrium should determine the actual substrate concentration.Hence, high pH values should be beneficial as well as using elevated substrate concentrations.However, these measures may also be counteracted by a decreasing activity of the biocatalyst under these conditions.Principally, electron withdrawing substituents should increase the enzyme rate by shifting the keto-enol equilibrium and lowering the redox potential on the one hand.On the other hand, the resulting radical might be too stable due to very low lying SOMO energy.
Obviously, the ratio of monomer to initiator has a strong influence on the average size of the resulting polymer.The number of growing polymer chains, competing for the remaining monomer reservoir, increases with initial initiator concentration (Figure 8) [44].
There is an ongoing discussion about the necessity of ß-diketones to initiate the polymerization reaction.Earlier reports on ß-diketone-free polymerization of acrylamide [13,50] could not be reproduced by others [48,51].One potential solution of this apparent discrepancy may be found in the very high H 2 O 2 concentration in the mediator-free polymerizations resulting in ‗unusual' heme-iron species [19].Thus, highly reactive peroxidase-species might initiate the polymerization reaction by direct H-atom abstraction from the monomer.Alternatively, oxidative degradation of heme resulting of Fe-release into the reaction medium might account for catalytic, Fenton-like generation of reactive oxygen species (ROS) initiating the polymerization reaction.
Kobayashi and coworkers reported on the mediator-free direct polymerization of acryl amide using the laccase from Pycnoporus coccineus suggesting a simplified polymerization scheme [52].Using the laccase from Myceliophthora thermophilia, this was not achieved [14,45] and a follow-up study validating Kobayashi's initial study is still missing.
Particularly when using laccases, molecular oxygen plays an ambivalent role.On the one hand, O 2 serves as stoichiometric oxidant to initiate the polymerization reaction.On the other hand, excess O 2 can also efficiently quench the radical polymerization [45,53].
Recently, Nieto et al. reported on an interesting approach to balance the in situ O 2 concentration for laccase-initiated polymerization by co-application of glucose oxidase as additional O 2 -consuming reaction [54].

Controlling Polymerization of Aromatics
In contrast to the above-mentioned polymerization of vinyl monomers, regioselectivity also plays an important role in the polymerization of phenols and anilines.Hence, many efforts have been directed towards gaining control over the chemo-and regioselectivity of the enzymatic polymerization of phenols and anilines.

Cosolvents
Also due to the poor aqueous solubility of most aromatic substrates, the influence of co-solvents is frequently addressed [55,56].In some cases significant control over the polymer size and polydispersity has been achieved with organic solvents.For example, Dordick et al. observed changes in the average polymer weight of poly(phenol) from 1,000 to over 26,000 g• mol −1 upon varying the 1,4-dioxane content in the polymerization reactions [57].Oguchi et al. reported on the HRP-initiated polymerization of phenol in aqueous methanol solutions yielding number average molecular weights up to 5200 g• mol −1 [58].Mita et al. have investigated various polar solvents and their influence on the chemoselectivity of the peroxidase-initiated polymerization of phenols (Figure 9) [59,60].Also the hydrophobicity of the starting material had an influence on the C-C vs. C-O selectivity: the higher the hydrophobicity, the higher was the C-C-selectivity.Later on the same authors substantiated these results also using laccase as catalyst [61,62].In addition to classical organic solvents, also ionic liquids have received some attention as cosolvents to increase the solubility of the phenolic monomers.Interestingly, while Sgalla et al. [63].reported the exclusive formation of dimers using HRP in [BMIM][BF 4 ], Eker et al. later on reported on the generation of comparably large polymers using the same IL as cosolvent [64].Obviously, more research will be necessary to fully understand the effect of ILs as cosolvents to support enzymatic polymerizations [65].
Ionic liquids can also be used as liquid support for enzyme immobilization as demonstrated by Rumbau et al. [66].HRP immobilized in [BMIM][PF 6 ] was applied in an emulsion polymerization of aniline (using dodecylbenzensulfonate as anionic template, vide infra).After the reaction, the aqueous product phase was separated from the enzyme-containing IL which could be reused at least 5 times without significant changes in the product properties (Figure 10).Cyclodextrines have been evaluated as alternatives to organic cosolvents to increase the solubility of hydrophobic phenols [67][68][69].Of course, (almost) non-aqueous reaction media would solve the solubility issue of phenols.Furthermore, anhydrous conditions can significantly alter the outcome of a given enzyme reaction.For example, as early as 1986, Dordick et al. reported that HRP catalyzes the depolymerization of lignin model compounds in 95% dioxane whereas under aqueous conditions no depolymerization activity was detectable [57,70].Of course the solubility of native polypeptides in non-aqueous reaction media is practically zero, leading to severe diffusion limitations when using immobilized biocatalysts.However, under certain conditions enzymes can be made organosoluble e.g., by chemical modification (acetylation), [57,70] or ion pairing with anionic surfactants [71] or calixarenes [72].For example, Li and coworkers could make HRP soluble in isooctane by ion pairing it with the anionic surfactant aerosol OT (AOT) (Figure 11).The resulting organosoluble HRP was used in the tBuOOH-driven polymerization of hexylphenol [71].

Templates
There are a number of investigations in which templates have been used for controlling the chemical structure of polymers synthesized by oxidoreductase-initiated polymerization.Very recently, Walde and Gou gave an excellent overview over the present state of the art [73], which is why here only a few representative examples are discussed.
Poly(styrenesulfonate) (PSS) represents one of the first an most widely applied templates to control polymerizations.Special interest has been paid to the polymerization of aniline to the conducting polymer form (emeraldine).In the absence of a suitable template aniline polymerizes with poor regioselectivity yielding complex, insoluble and non conducting polymers.However, e.g., in the presence of negatively charged PSS (and in the presence of protonated aniline, i.e., at suitable pHs) formation of the conducting emeraldine form is strongly favored (Figure 12) [27,[73][74][75][76][77][78][79].

Figure 12.
Reaction products obtained by radical polymerization (e.g., in the system HRP/H 2 O 2 ) of aniline.In the absence of templates (upper) and e.g., using PSS as template.
Other negatively charged polymers [80] such as poly(vinylphosphonic acid) [81]or DNA [82][83][84] have been reported as templates.The templates promote the formation of the electrically conducting emeraldine form of poly(aniline) and significant branching (as in case of in the absence of the templating agent) does not occur.The template is thought to at least partially lead to a proper alignment of the monomers and the growing chain; another role of the negatively charged template is to serve as counter ion (dopant) influencing the charge and conformation of the polyaniline and thereby its electronic properties.In addition, anionic surfactants under emulsion conditions have been reported as templates [85,86].Using PSS as template also proved to be suitable to produce poly(pyrroles) with improved conductiveness [87].
Another very interesting templating effect was reported by Xu et al. who caffeic acid onto a p-aminothiophenol-modified gold surface [94].Oriented adsorption of the phenolic monomer was achieved via inonic and H-bond interactions of the substrate with the amino-modified surface.As a result, the laccase-or HRP-initiated polymerization proceeded with very high phenylene selectivity whereas under ‗normal aqueous' polymerization conditions a mix of phenylene and oxyphenylene connections was observed (Figure 13).

Substrate Engineering
Also the structure of the monomers themselves can significantly influence the selectivity of the polymerization reaction.For example Mita et al. [60] showed that the phenylene content of poly(p-substituted phenols) increased with the hydrophobicity of the substituent.Blocking the o-position of aniline enabled selective polymerization of anilines yielding conductive emeraldines without the need for a template [27].
Another interesting example is the polymerization of p-hydroxy benzoic acid (derivates), which proceeds highly regioselectively producing oxyphenylene connections exclusively (Figure 14) [95].Polymerization of catechols and hydroquinones can be tedious due to facile oxidation to the corresponding quinones.This can be overcome by blocking of one of the OH-functionalities as demonstrated by Dordick and coworkers (Figure 15) [96].As a result, not only was quinine formation efficiently suppressed but also a high level of o-phenylene selectivity achieved.In a similar approach 4-amino phenol was selectively polymerized by reversible blocking of the amino group via imine formation [97].

Selected Examples
There is an enormous amount of structurally diverse phenols, anilines and other aromatic monomers, which have been subjected to enzyme-initiated radical polymerization.A representative, but by far not exhaustive selection of the different monomers is given in Figures 16 and 17.For a detailed discussion about polymer properties and potential uses, the interested reader is referred to some excellent previous overviews [8][9][10][11][12].

Polyphenols
Flavonoids represent a class of natural secondary metabolites that have found numerous applications in human health products.Especially their antioxidant and radical scavenging activity but also anti microbial properties make this product class interesting.The group around Kobayashi has investigated the production and properties of polymerized polyphenols [11].Interestingly, in the majority of these examples, the antioxidant activity (and quite frequently also other health properties) are significantly increased as compared to the monomers.A unifying explanation for this observation is missing so far.
Early reports dealing with modified flavonids concern the direct laccase-and/or peroxidase-mediated polymerization of the monomers.More recently, oxidative conjugation to other polymers has gained considerable interest (Figure 18).Table 2 gives an overview over the polymeric products reported.
As mentioned above, the oxidative grafting of flavonoids to polymers is enjoying increased attention especially aiming at functionalized textiles or food applications [130].
One of the first examples for this was reported by Kobayashi and coworkers who oxidatively grafted poly(allylamine) with catechin (Figure 19) [131], which was followed up more recently by Rao and coworkers [132,133].Instead of poly(allylamine) also natural polymeric support can be used resulting in a composite with similarly superior antioxidant activity as compared to the catechin monomer.For example gelatin was grafted with catechin [134].Wool can also be grafted e.g., with gallates resulting in composites with antioxidant and antimicrobial activity [135].When using gallic acid esters, increased water repellence was achieved.Chitosan-composites with gallic acid (derivates) [136][137][138][139], ferulic acid [140], flavonoids [141] exhibit increased antioxidant activity.An interesting extension of this concept is to use amine-functionalized inorganic supports [142].
A practical application of this grafting technology may be in the textile and food industry yielding products with antimicrobial activity and modified rheological properties [130,138,139,[143][144][145][146].

Polymer Modification
Oxidoreductase-initiated covalent linkage of phenols has also received considerable interest for the cross-linking of polymers to form biocompatible hydrogels.For example, proteins presenting tyrosine moieties at their surface can be gelled in the presence of laccases or peroxidases/H 2 O 2 (Figure 20) [147][148][149][150]. Next to proteins also natural polymers exhibiting phenolic side chains can be gelled enzymatically.For example pectins contain some ferulic acid which can be used for oxidative crosslinking of the pectin chains for irreversible gellation [151][152][153].However, even if no phenolic side chain is present in the polymer, it may be introduced chemically.In that respect, tyramine has gained some popularity e.g., for the crosslinking of carboxymethyl cellulose [154], alginate [155], hyaluronic acid [156], dextran [157] or artificial polymers such as Tetronic [158].
For example, tyrosinases generate reactive quinones from phenols, which can react with chitosan [141,145,160,161].Similarly, reactive quinones can be generated using laccases [140,146] of peroxidases [136,139].A very creative application of the system HRP/H 2 O 2 /Acac for graft polymerization of acryl amide on starch was reported recently by Biswas and coworkers [114].A biocatalytic alternative route to the established cerium(IV)-based routes to poly(acrylate)-grafted starch with applications as superabsorbers or performance additives in paper making or textile sizing was reported.Under non-optimized conditions grafting efficiencies of up to 65% are reported.The authors suggest covalent attachment of the poly(acrylamide) chain to the starch backbone via H-abstraction at the glycosidic C-atom (Figure 22).Poly(acrylamide) grafting onto lignin has been reported in the presence of organic hydroperoxides [162,163].The proposed mechanism (Figure 23.) comprises laccase-catalyzed H-atom abstraction from phenolic lignin residues.The resulting phenoxy radicals interact with the peroxides generation alkoxy-and hydroperoxy-radicals, which are supposed to initiate the acrylamide polymerization process.Grafting of poly(acrylamide) onto lignin is proposed to occur through recombination of the respective radicals.

Artificial Urushi
Urushiols are a class of natural alkyl-substituted phenols and catechols (Figure 24), which in the presence of laccase can polymerize to form Urushi, a natural lacquer used e.g., in traditional Japanese artwork.

Selected Examples for Chemoselective Polymerization
One advantage of oxidoreductase-catalysis that is frequently mentioned is its high selectivity.As mentioned above, so far no examples of stereospecificity have been reported in enzyme initiated polymerization, and are not very likely to come up in the near future.However, there is a range of examples demonstrating chemoselective radical formation, which will be shortly outlined below.
The selective polymerization of bifunctional monomers containing vinyl and phenol moieties.Generally, laccases and peroxidases act on the phenol part selectively leading to vinyl-substituted poly(phenols) which then are available for further modification (Figure 26) [68,101,171].
A very nice example for the potential of biocatalysis as complementary tool to established chemocatalysis was reported using m-ethinylphenol as monomer [106].Subjecting this compound to HRP/H 2 O 2 , poly(phenol) formation was the only reaction observed wile leaving the ethinyl group untouched.In contrast, Cu I catalysts lead to dimerization via the ethinyl function (Figure 27).Another example for chemoselectivity of enzymatic polymerization was reported by Bilici et al. [172].
Here, an aldehyde-bearing catechols was polymerized enzymatically without oxidizing the aldehyde moiety.

Phenol Detoxification
A good portion of and peroxidase literature deals with bioremediation and pollutant control [130,[173][174][175].The removal of phenolics is rather straightforward as these compounds are generally oxidized by the laccases or peroxidases directly [176].In most of the cases, the detoxification mechanism is based on the formation of insoluble oligomeric or polymeric products which can then be removed by filtration.

Conclusions
Enzymatic reactions are enjoying increasing attention as alternatives to classical chemical routes.‗The hallmark of enzyme catalysis is its superior catalytic power and high selectivity under mild reaction conditions' [199].Furthermore, enzyme catalysis generally exhibits high chemo-, regio-, and enantioselectivity.In the context of oxidoreductase initiated radical polymerizations these advantages come into play only to a limited extent.Mostly the role of the enzyme is confined to the generation of a starter radical.Thus, enzyme-initiated polymerizations comprise all characteristics of a classical chemical polymerization.
Admittedly, enzymatic routes offer various handles to control polymer weight with enzyme concentration being the most efficient one.Furthermore, enzymes are derived from renewable feedstock and therefore can be considered more benign than many classical initiators.Overall, enzyme-initiated polymerization represents a promising alternative approach to the established chemical routes.Implementation on industrial scale will not occur on a short-term due to cost limitations but may eventually result in significantly greener production routes (though a full life cycle analysis will be necessary as enzymatic reactions are not per se greener than their chemical counterparts).Furthermore, it represents another example that enzyme catalysis is not confined to its traditional playgrounds such as chiral molecules.

Figure 1 .
Figure 1.Resting state of heme peroxidases.In the majority of cases L constitutes a histidine ligand.

Figure 3 .
Figure 3. Bienzymatic polymerization reaction.Glucose oxidase (GOx) catalyzes the reduction of O 2 to H 2 O 2 which then initiates the polymerization reaction.

Figure 4 .
Figure 4.In situ formation of peracetic acid from a solvent stabilizer to initiate horseradish (HRP)-catalyzed polymerizations.

Figure 8 .
Figure 8. Influence of the monomer-mediator ratio on the properties of poly(acrylamide).

Figure 9 .
Figure 9. Influence of cosolvent on the peroxidase-initiated polymerization of 4-butylphenol.left: influence of different logPs on the selectivity of the bond formation and polymer weight; right: chemoselectivity at different co-solvent concentrations.

Figure 16 .
Figure 16.Representative (and not exhaustive) selection of phenol monomers polymerized using oxidoreductases.

Figure 17 .
Figure 17.Representative selection of vinyl monomers polymerized by oxidoreductase catalysis.

Figure 27 .
Figure 27.Complementary conversion of m-ethinylphenol using HRP or Cu I .

Table 1 .
Influence of various β-diketone mediators in the polymer properties.