Metallopolymers for catalytic generation of hydrogen

Abstract

Metallopolymers composed of polymers and catalytically active diiron-disulfide ([2Fe-2S]) complexes are described herein. [FeFe]-hydrogenase mimics have been synthesized and used to initiate polymerization of various monomers to generate metallopolymers containing active [2Fe-2S] sites which serve as catalysts for a hydrogen evolution reaction (HER). Vinylic monomers with polar groups provided water solubility relevant for large scale hydrogen production, leveraging the supramolecular architecture to improve catalysis. Metallopolymeric electrocatalysts displayed high turnover frequency and low overpotential in aqueous media as well as aerobic stability. Metallopolymeric photocatalysts incorporated P3HT ligands to serve as a photosensitizer to promote photoinduced electron transfer to the active complex.

Claims

1. An electrocatalytic metallopolymer for generating hydrogen (H.sub.2), said metallopolymer comprising an electrocatalytically active complex bonded to a polymer, wherein the metallopolymer accepts electrons and generates H.sub.2; wherein the metallopolymer is according to the following: Complex-L.sub.1-(Polymer).sub.i, wherein i is 1 or 2; wherein the electrocatalytically active complex is the following: ##STR00018##

2. The metallopolymer of claim 1, wherein L.sub.1 is the following: ##STR00019## wherein a phenyl group of L.sub.1 is bonded to the complex.

3. The metallopolymer of claim 1, wherein the polymer is according to the following: ##STR00020## wherein X is I, Br or Cl, wherein m ranges from about 1-1,000, wherein n ranges from about 1-1,000, wherein A and B are each derived from an unsaturated monomer, and wherein A is identical to B or A is different from B.

4. The metallopolymer of claim 3, wherein the polymer imparts water solubility to the metallopolymer.

5. The metallopolymer of claim 1, wherein the metallopolymer complex is according to any one of the following: ##STR00021## wherein m ranges from about 1-100, wherein n ranges from about 1-1,000, and wherein p ranges from about 1-1,000.

6. The metallopolymer of claim 1, wherein the metallopolymer complex is soluble in organic or aqueous solutions.

7. The metallopolymer of claim 1, wherein the metallopolymer complex has an M.sub.w:M.sub.n ratio that is less than about 1.3.

8. The metallopolymer of claim 1, wherein the metallopolymer complex is capable of generating H.sub.2 from aqueous solutions.

9. The metallopolymer of claim 1, wherein the metallopolymer complex is stable when exposed to an aerobic environment.

10. The metallopolymer of claim 9, wherein the metallopolymer complex maintains stability when exposed to the aerobic environment during H.sub.2 generation.

11. The metallopolymer of claim 1, wherein the metallopolymer complex has a turn over frequency of at least about 10.sup.3 k(s.sup.−1) in water.

12. The metallopolymer of claim 1, wherein the metallopolymer complex has an overpotential of at most about 700 mV in water.

13. A method of generating molecular hydrogen (H.sub.2), said method comprising: a) providing the electrocatalytic metallopolymer according to claim 1; b) adding the electrocatalytic metallopolymer to an organic or aqueous electrolyte solution to form an electrocatalytic mixture; and c) performing electrolysis using the electrocatalytic mixture, wherein the electrocatalytic metallopolymer accepts electrons from a cathode, generating a reduced form of the electrocatalytic metallopolymer which is protonated by some protic species in solution, thereby reducing protons in the electrolyte solution to produce H.sub.2.

14. The method of claim 13, wherein the electrolyte solution comprises water, tetrahydrofuran, acetonitrile, alcohol, ammonium, alkyl ammoniums, sulfonic acids, carboxylic acids, or a combination thereof.

15. A method of producing the electrocatalytic metallopolymer according to claim 1, said method comprising: a) providing a metalloinitiator according to the following structure: ##STR00022## b) providing an unsaturated monomer; c) providing a transition metal catalyst; d) providing a ligand; e) mixing the transition metal catalyst and ligand to form a metal-ligand catalyst; and f) mixing and heating the metalloinitiator, unsaturated monomer, and metal-ligand catalyst to activate an atom-transfer radical-polymerization (ATRP) reaction, thereby forming the electrocatalytic metallopolymer.

16. The method of claim 15, wherein providing the metalloinitiator comprises: a. providing a hydroquinone complex according to the following structure: ##STR00023## b. providing α-bromoisobutyryl bromide (BIBB); and c. mixing the hydroquinone complex and BIBB, wherein the BIBB esterifies the hydroquinone complex to produce the metalloinitiator.

17. An electrocatalytic metallopolymer for generating hydrogen (H.sub.2), said metallopolymer comprising a metallopolymer complex according to Formula 1: ##STR00024## wherein X is I, Br or Cl, wherein m ranges from about 1-1,000, wherein n ranges from about 1-1,000, wherein A and B are each derived from an unsaturated monomer, and wherein A is identical to B or A is different from B.

18. An electrocatalytic metallopolymer for generating hydrogen (H.sub.2), said metallopolymer comprising an electrocatalytically active complex bonded to a polymer, wherein the metallopolymer accepts electrons and generates H.sub.2, wherein the metallopolymer is according to the following: Complex-L.sub.1-(Polymer).sub.i, wherein i is 1 or 2; wherein the polymer is according to the following: ##STR00025## wherein X is I, Br or Cl, wherein m ranges from about 1-1,000, wherein n ranges from about 1-1,000, wherein A and B are each derived from an unsaturated monomer, and wherein A is identical to B or A is different from B.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The features and advantages of the present invention will become apparent from a consideration of the following detailed description presented in connection with the accompanying drawings in which:

(2) FIG. 1 shows a non-limiting embodiment of a metallopolymer catalyst of the present invention.

(3) FIG. 2 shows [FeFe]-Hydrogenase, its active site and the elementary reaction for H.sub.2 generation.

(4) FIG. 3 shows a reaction scheme for synthesizing the metalloinitiator and the metallopolymer. Non-limiting examples of vinylic monomers to prepare the metallopolymer are also shown.

(5) FIG. 4 shows a reaction scheme for synthesizing the metallopolymer via ATRP. Non-limiting examples of ATRP ligands and vinylic monomers to prepare the metallopolymer are also shown.

(6) FIG. 5 shows homogeneous methacrylate-based, polymer-supported electrocatalysts, PMMA-g-[2Fe-2S] in organic media, PDMAEMA-g-[2Fe-2S] and PEGMA-g-[2Fe-2S] in aqueous media.

(7) FIG. 6 shows an ORTEP diagram of the initiator with hydrogen atoms omitted and thermal ellipsoids shown at 50% probability level.

(8) FIG. 7 shows UV-Vis absorption spectra of the ATRP metalloinitiator and a PMMA-g-[2Fe-2S] metallopolymer in toluene. The PMMA-g-[2Fe-2S] metallopolymer was made using the ATRP metalloinitiator.

(9) FIG. 8 shows GPC data of PMMA-g-[2Fe-2S] with a UV-Vis detector operating at 254 nm, 350 nm, or 400 nm.

(10) FIGS. 9A and 9B show GPC data for PMMA-g-[2Fe-2S] (Mn=7,194 g/mol, Mw/Mn=1.06) and PDMAEMA-g-[2Fe-2S] (Mn=9,500 g/mol, Mw/Mn=1.33), respectively, with a UV-Vis detector operating at 400 nm, which is characteristic of the initiator, but not for PMMA or PDMEAMA polymers.

(11) FIG. 10 is an IR overlay of the initiator, PMMA, PDMAEMA, and PEGMA showing retention of characteristic Fe—CO stretching frequencies.

(12) FIG. 11 shows cyclic voltammetry (CV) of the metalloinitiator and PMMA-g-[2Fe-2S] in acetonitrile to observe Fe(I) to Fe(0) reduction in the metallopolymer.

(13) FIG. 12 is an exemplary schematic of a CV experiment to measure current from H.sub.2 generation.

(14) FIG. 13 shows CV electrocatalysis of the metalloinitiator with increasing [AcOH] in acetonitrile.

(15) FIG. 14 shows CV electrocatalysis of PMMA-g-[2Fe-2S] with increasing [AcOH] in acetonitrile.

(16) FIG. 15 shows an exemplary scheme of proton shuttling in PDMAEMA-g-[2Fe2S]. The amines in PDMAEMA are partially protonated at neutral pH which may facilitate proton transport and form an H-bond to the Fe—Fe center.

(17) FIG. 16 is a CV current density comparison of 100 μM PDMAEMA-g-[2Fe-2S] metallopolymer to a Pt electrode for H.sub.2 generation under identical conditions.

(18) FIG. 17 is a CV current density comparison of PDMAEMA-g-[2Fe-2S] and PMMA-g-[2Fe-2S] metallopolymers for H.sub.2 generation under identical conditions.

(19) FIG. 18 is a CV current density comparison of 0.10 mM PDMAEMA-g-[2Fe-2S] and 0.52 mM PEGMA-g-[2Fe-2S] metallopolymers to a Pt electrode for H.sub.2 generation under identical conditions.

(20) FIG. 19 is a CV current density comparison of 0.1 mM PDMAEMA-g-[2Fe-2S], 0.52 mM PEGMA-g-[2Fe-2S], and 0.2 mM PDMAEMA-r-PEGMA-g-[2Fe-2S] copolymer to a Pt electrode for H.sub.2 generation under identical conditions.

(21) FIG. 20 shows cyclic voltammetry comparison of anaerobic and aerobic activity of PDMAEMA-g-[2Fe-2S] (ca. 50 μM [2Fe-2S] via IR, 2.5 mg/mL). Freshly prepared anaerobic solution, initial aerobic current response, current response after 18 hours of storage under aerobic conditions, and recovery of current upon return to anaerobic conditions. Current has been normalized to current density by dividing by experimentally determined area of the glassy carbon electrode (A=0.07469 cm.sup.2).

(22) FIG. 21 shows non-limiting examples of metallopolymers that are synthesized using Fe.sub.2S.sub.2(CO).sub.6 complexes with P3HT and other polymeric ligands to enable photogeneration of H.sub.2 and alkylation of diiron-disulfide complexes with Grignard, or organolithium reagents and alkyl halides to form unsymmetric complexes, or A-B diblock metallopolymers.

(23) FIG. 22 shows a non-limiting example of a reaction scheme for preparing unsymmetric metallopolymer complexes.

(24) FIG. 23 shows an exemplary reaction scheme for (a) synthesis of Fe.sub.2S.sub.2(CO).sub.6 disulfide complex; (b) Grignard terminated regioregular P3HT; and (c) unsymmetric diiron complex via reaction of P3HT-MgX and alkylation with benzyl halides.

(25) FIG. 24 shows an exemplary reaction scheme for (a) synthesis of benzyl halide terminated polystyrene and poly(t-butyl acrylate) followed by (b) alkylation of reactive P3HT thiolates with these polymeric benzyl halides (BnBr) to form A-B diblock metallopolymers (c) synthesis of water dispersable A-B diblocks via alkylation of poly-(t-BA) and deprotection with TFA.

(26) FIG. 25 shows an exemplary reaction scheme for (a) proposed synthesis of phosphine terminated P3HT ligands and (b) preparation of metallopolymer complexes with mono, or bis-P3HT ligands.

(27) FIG. 26 is a non-limiting example catalytic generation of H.sub.2 with benzoFe.sub.2S.sub.2(CO).sub.6 (Benzcat).

(28) FIG. 27 shows a non-limiting example of a photocatalytic HER scheme.

(29) FIG. 28 shows a Gas Chromatogram (GC) of H.sub.2 peak in overhead gasses upon irradiation of Benzcat, P3HT, and PhSH in toluene (red trace, left y-axis) and the control experiment without P3HT (blue trace, right y-axis). A third control without Benzcat did not produce detectable amounts of H.sub.2 under the same conditions (data not shown).

(30) FIG. 29 shows Ultraviolet Photoelectron Spectroscopy (UPS) data for Benzcat showing an ionization onset (HOMO energy) at 7.50 eV.

(31) FIG. 30 shows CV of Benzcat (1 mM) in CH.sub.3CN with increasing catalytic current and increasing amounts of acetic acid.

(32) FIG. 31 shows absorption spectra for monothiophene complex (dotted lines) and terthiophene complex (solid lines) in various solvents at equal concentrations.

DESCRIPTION OF PREFERRED EMBODIMENTS

(33) As known to one of ordinary skill in the art, an atom transfer radical polymerization (ATRP) is a method of controlled radical polymerization (CRP) where an alkyl halide (e.g. R-X, X: Br or Cl) is activated by a transition metal complex (e.g. cuprous halide salts with amine, or N-heterocyclic ligands, such as Cu′Br with bipyridine ligands) to form an active radical that reacts with a vinyl group (i.e. monomer) and the intermittently formed radical reacts with additional monomer units for propagation to put monomers together in a piece-by-piece fashion. The ATRP method enables the creation of a wide range of polymeric materials with a controlled molecular weight and molecular weight distribution using monomers with different functionalities for specific target applications.

(34) Referring now to FIG. 1-20, in one embodiment, the present invention features an electrocatalytic metallopolymer for generating hydrogen (H.sub.2). According to some embodiments, the metallopolymer may comprise an electrocatalytically active complex bonded to a polymer. For example, the metallopolymer may be according to the following: Complex-L.sub.1-(Polymer).sub.i, where i may be 1 or 2.

(35) In some embodiments, the electrocatalytically active complex may be the following:

(36) ##STR00003##

(37) In other embodiments, L.sub.1 may be the following:

(38) ##STR00004##

(39) In some embodiments, a phenyl group of L.sub.1 may be bonded to the complex. For example, the phenyl group of L.sub.1 may be bonded to the disulfide group of the complex.

(40) In still other embodiments, the polymer may be according to the following:

(41) ##STR00005##

(42) In some embodiments, X may be I, Br or Cl. In some embodiments, m and n can each range from about 1-1,000. In other embodiments, A and B may each be derived from an unsaturated monomer. In one embodiment, A may be identical to B. In an alternative embodiment, A may be different from B. In preferred embodiments, the polymer can impart water solubility to the metallopolymer. Further still, the polymer can function to site-isolate the complex during electrocatalysis, thus improving the electrocatalytic lifetime and stability of the metallopolymer.

(43) According to other embodiments, the electrocatalytic metallopolymer for generating hydrogen (H.sub.2) may comprise a metallopolymer complex according to Formula 1:

(44) ##STR00006##

(45) In some embodiments, X may be I, Br or Cl. In some embodiments, m and n can each range from about 1-1,000. In other embodiments, A and B may each be derived from an unsaturated monomer. In one embodiment, A may be identical to B. In an alternative embodiment, A may be different from B.

(46) Consistent with any embodiment of the metallopolymer, the unsaturated monomer may be water-soluble. In one embodiment, the unsaturated monomer may be a vinylic monomer. In some embodiments, the vinylic monomer may be a styrenic monomer, a methacrylate monomer, an acrylate monomer, or functional analogues thereof. For example, the vinylic monomer may be methyl methacrylate, 2-(dimethylamino)ethyl methacrylate, poly(ethylene glycol) methacrylate, styrene (Sty), Sty-SO.sub.3Na, or Sty-NR.sub.2, where R.sub.2 is H or CH.sub.3.

(47) In other embodiments, the vinylic monomer may comprise a functional water-soluble group that imparts water solubility to the metallopolymer. Non-limiting examples of the functional water-soluble group include alcohols, amines, amides, esters, carboxylic acids, sulfonic acids, ammonium groups, carboxylate groups, sulfonate groups, or ether groups. In some embodiments, the ether group may be an oligo(ethylene glycol) or a poly(ethylene glycol).

(48) According to yet other embodiments, the electrocatalytic metallopolymer for generating hydrogen (H.sub.2) may comprise a metallopolymer complex according to Formula 2:

(49) ##STR00007##

(50) In some embodiments, X may be I, Br or Cl. In some embodiments, n can range from about 1-1,000. In other embodiments, R may be Ph, Ph-NR.sub.2, Bn-NR.sub.2, Ph-SO.sub.3Na, COOCH.sub.3, COOBn, COO(CH.sub.2).sub.2N(CH.sub.3).sub.2, COO(CH.sub.2).sub.2N(CH.sub.2CH.sub.3).sub.2 or COO((CH.sub.2).sub.2O).sub.mCH.sub.3. In further embodiments, R.sub.1 and R.sub.2 may individually be H or CH.sub.3. In still further embodiments, m can range from about 1-100.

(51) Examples of the metallopolymer complex according to Formula 1 or 2 include, but are not limited to, the following:

(52) ##STR00008##

(53) In accordance with the aforementioned examples, m can range from about 1-100. In some embodiments, n and p can each range from about 1-1,000.

(54) Consistent with any of the electrocatalytic metallopolymers described herein, the metallopolymer complex may be soluble in organic or aqueous solutions. In preferred embodiments, the metallopolymer complex is preferably capable of generating Hz from the organic or aqueous solutions. In other preferred embodiments, the metallopolymer complex may be stable when exposed to an aerobic environment. For example, the metallopolymer complex can maintain stability when exposed to the aerobic environment, such as O.sub.2 bubbles, during Hz generation.

(55) In some embodiments, the metallopolymer complex may have an Mw:Mn ratio that is less than about 1.3. For example, the Mw:Mn ratio can range from about 1.01 to 1.30 In other embodiments, the metallopolymer complex may have a high turnover frequency. For example, the turnover frequency may be at least about 10.sup.3 k(s.sup.−1) in water. In further embodiments, the metallopolymer complex may have an overpotential of at most about 700 mV in water.

(56) Since, in one aspect, the present invention provides electrocatalytic metallopolymers for generating H.sub.2, it is another objective of the present invention to provide methods for generating molecular hydrogen (H.sub.2). In one embodiment, the method may comprise providing any of the electrocatalytic metallopolymers described herein, adding the electrocatalytic metallopolymer to an organic or aqueous electrolyte solution to form an electrocatalytic mixture, and performing electrolysis using the electrocatalytic mixture. Without wishing to be bound by a particular theory or mechanism, the electrocatalytic metallopolymer can accept electrons from a cathode, thereby generating a reduced form of the electrocatalytic metallopolymer, which is then protonated by some protic species in solution. Thus, the protons in the electrolyte solution are reduced to produce Hz. Examples of the electrolyte solution include, but are not limited to, water, tetrahydrofuran, acetonitrile, alcohol, ammonium, alkyl ammoniums, sulfonic acids, carboxylic acids, or combinations thereof.

(57) According to other embodiments, the present invention may feature methods of producing any of the electrocatalytic metallopolymers described herein. In some embodiments, the method may comprise providing a metalloinitiator according to the following structure:

(58) ##STR00009##

(59) In some embodiments, the metalloinitiator is prepared by providing α-bromoisobutyryl bromide (BIBB) and a hydroquinone complex according to the following structure:

(60) ##STR00010##

(61) The hydroquinone complex and BIBB may be combined and mixed together so that the BIBB esterifies the hydroquinone complex to produce the metalloinitiator.

(62) After providing a metalloinitiator, the method may further comprise providing an unsaturated monomer, providing a transition metal catalyst, providing a ligand, mixing the transition metal catalyst and ligand to form a metal-ligand catalyst, and mixing and heating the metalloinitiator, unsaturated monomer, and metal-ligand catalyst to activate an atom-transfer radical-polymerization (ATRP) reaction, thereby forming the electrocatalytic metallopolymer. In some embodiments, the transition metal catalyst may comprise a copper complex such as Cu(I)Br. In other embodiments, the ligand may be N,N,N′,N″,N″-pentamethyldiethylenetriamine, 1,1,4,7,10,10-hexamethyltriethylenetetramine, or 4,4′-dinonyl-2,2′-dipyridyl.

(63) In preferred embodiments, the unsaturated monomer may be water-soluble. In one embodiment, the unsaturated monomer may be a vinylic monomer. In some embodiments, the vinylic monomer may be a styrenic monomer, a methacrylate monomer, an acrylate monomer, or functional analogues thereof. For example, the vinylic monomer may be methyl methacrylate, 2-(dimethylamino)ethyl methacrylate, poly(ethylene glycol) methacrylate, styrene (Sty), Sty-SO.sub.3Na, or Sty-NR.sub.2, where R.sub.2 is H or CH.sub.3.

(64) In other embodiments, the vinylic monomer may comprise a functional water-soluble group that imparts water solubility to the metallopolymer. Non-limiting examples of the functional water-soluble group include alcohols, amines, amides, esters, carboxylic acids, sulfonic acids, ammonium groups, carboxylate groups, sulfonate groups, or ether groups. In some embodiments, the ether group may be an oligo(ethylene glycol) or a poly(ethylene glycol).

(65) In further embodiments, the electrocatalytic metallopolymers of the present invention may be disposed or incorporated into a chromophore. Without wishing to limit the invention to a particular theory or mechanism, this incorporation of the metallopolymers into chromophores may advantageously allow for photocatalysis using said metallopolymers to generate H.sub.2. For instance, the metallopolymers in the chromophores may be exposed to a light source, such as UV or visible light, which initiates the HER.

Electrocatalyst Examples

(66) The following are non-limiting examples of the present invention. It is to be understood that said examples are provided for the purpose of demonstrating the present invention in practice, and is in no way intended to limit the invention. Equivalents or substitutes are within the scope of the invention.

(67) In some embodiments, the strategy for incorporation of [2Fe-2S] complexes into polymer architectures comprises the synthesis of a difunctional ATRP initiator bearing the [2Fe-2S] moiety. A difunctional initiator allows for polymer growth from both sides of the complex, ideally giving a central active site protected from known associative reactions. With this modular approach, the synthesis of many different polymeric systems around a common [2Fe-2S] core makes it possible to tune the polymer architecture to improve catalysis via modulation of the secondary coordination sphere by including flexible R—NMe.sub.2 groups.

Experimental

(68) All synthesis and electrochemical experiments were carried out under an atmosphere of argon and using anhydrous, deoxygenated solvents and Schlenk techniques unless otherwise noted. Cyclic voltammetry experiments were performed with a Gamry Reference 3000 or Gamry Reference 1000 was used for the collection of all electrochemical data. All potentials in acetonitrile (ACN) were referenced to the Fc/Fc+ couple. Potentials in water are referenced to SHE using the standard conversion of 0.210 V vs. Ag/AgCl/3M KCl. The working electrodes (3 mm PEEK-encased glassy carbon and 1.5 mm PEEK encased Pt, BASi) were polished using a Buehler microcloth with 1.0 then 0.05μ alumina micropolish suspended in de-ionized water, then briefly (ca. 10 s) sonicated in distilled water. A Pt mesh was used as the counter-electrode. A silver wire in 0.01 M AgNO.sub.3 was used as a reference electrode in acetonitrile. A silver wire coated with a layer of AgCl suspended in 3.0 M KCl was used for water experiments. In both cases the reference electrode was separated from the analyte solution by a Vycor frit.

Synthesis of [2Fe-2S]-Initiator [μ-2,3-(naphthalene-1,4-diyl bis(2-bromo-2-methylpropanoate) dithiolato]bistricarbonyliron (5)

(69) Referring to FIG. 3, metalloinitiator 5 for ATRP was prepared in three steps starting with the known complex NHQ-CAT. Sufficient NaCNBH.sub.3 (2.26 mg, 0.036 mmol) was added to NHQ-CAT (45 mg, 0.90 mmol) in THF (2 mL) to reduce the quinone and the solution was stirred at room temperature for 2 h. Triethylamine (TEA) (75 μL, 0.54 mmol) was then added via micro syringe and the solution was stirred for 20 minutes. α-Bromoisobutyryl bromide (BIBB) (30 μL, 0.22 mmol) was added for esterification of NHQ-CAT via micro syringe and the solution was stirred at room temperature for 2.25 h. The reaction was filtered to remove precipitate and solvent removed by rotary evaporation (23° C., ca. 200 torr) to yield a red/orange solid. Purification via column chromatography on silica gel (30% DCM in hexane) gave 63 mg of 5 (0.079 mmol, 87%) as a powdery orange solid upon removal of solvent. This solid was recrystallized via layering of toluene/MeOH to obtain crystals for electrochemical experiments and polymer synthesis. The structure of metalloinitiator 5, shown in FIG. 6, was unequivocally confirmed by single crystal X-ray crystallography. .sup.1H NMR: (CDCl.sub.3, 500 MHz, 298 K) δ (ppm) 7.81 (2H, dd J=6.5, 3.4 Hz) 7.49 (2H, dd J=6.5, 3.4 Hz), 2.19 (12H, s) .sup.13C NMR: (CDCl.sub.3, 125 MHz, 298 K) δ (ppm) 206.8 (OC—Fe), 168.3 (C═O), 143.0 (C.sub.1,4-O), 134.8 (C.sub.,2,3-S), 129.1 (C.sub.6,7-H), 128.1 (C.sub.9,10), 121.9 (C.sub.5,8-H), 54.8 (CH—Br), 31.0 (CH.sub.3) IR (CHCl.sub.3, thin film on NaCl): 3688 cm.sup.−1 (w), 3619 cm.sup.−1 (w, C.sub.sp2—H), 3154 cm.sup.−1 (w, C.sub.sp2—H), 3019 cm.sup.−1 (vs, Csp2-H), 2976 cm.sup.−1 (w, Csp3-H), 2082 cm.sup.−1 (Fe—CO, s), 2050 cm.sup.−1 (Fe—CO, s), 2012 cm.sup.−1 (Fe—CO, s) 1760 cm.sup.−1 (C═O ester, w), 1522 cm.sup.−1 (C═C, w), 1423 cm.sup.−1 (C—H, w), 1210 cm.sup.−1 (C—O, vs)

Synthesis of [2Fe-2S] Metallopolymers via ATRP

(70) The growth of well-defined (co)polymers from the [2Fe-2S] metalloinitiator 5 via ATRP is a unique method among polymeric-[2Fe-2S] systems as it provides a facile method to tune the environment around the catalyst core in a single step by variation of comonomer feed and chain length of the covalently tethered macromolecules without post-polymerization modification. The synthesis of metallopolymers was initially investigated by the ATRP of methyl methacrylate (MMA) to confirm the chemical tolerance of the [2Fe2S] complex to polymerization conditions and facilitate characterization of metallopolymers using conventional polymer solution characterization in non-polar media.

PMMA-g-[2Fe-2S] Metallopolymers

(71) Referring to FIG. 4, PMMA metallopolymers (PMMA-g-[2Fe-2S]) were prepared using metalloinitiator 5 as a difunctional ATRP initiator with a copper (I) bromide (Cu(I)Br)/4,4′-Dinonyl-2,2′-dipyridyl (dNbpy) catalyst system at 55° C. Molar masses of ca. 10,000 g/mol (i.e., 5,000 g/mol per each initiator site) were targeted to enable sufficient site isolation of the iron complex, while still being amenable to size exclusion chromatography (SEC) and NMR spectroscopy end-group analysis for molecular weight characterization.

(72) The successful formation of well-defined PMMA-g-[2Fe-2S] metallopolymers (M.sub.n, SEC=11,982 g/mol; M.sub.w/M.sub.n=1.10) was confirmed using a combination of IR spectroscopy of the characteristic Fe—CO stretching frequencies (FIG. 10) along with size exclusion chromatography (SEC) in tetrahydrofuran (THF) coupled with UV-vis detection (at 400 nm) (FIG. 9A) and end-group analysis using .sup.1H NMR spectroscopy (not shown). Furthermore, PMMA-g-[2Fe-2S] metallopolymers were found to be electrocatalytic active for HER in acetonitrile in the presence of AcOH (FIG. 14).

PDMAEMA-g-[2F-2S] Metallopolymers

(73) Upon structural confirmation that well-defined [2Fe-2S] metallopolymers could be prepared via the ATRP methodology, the preparation of water soluble materials was then pursued, particularly with the aim of engineering the microenvironment around the [2Fe—S2] complex to enhance HER electrocatalysis. To achieve this goal, tertiary amines were incorporated as side chain groups to metallopolymers to impart both water solubility to these complexes, and facilitate proton transfer to the [2Fe-2S] core upon protonation of the amine groups. These metallopolymers were prepared by ATRP of 2-(dimethylamino)ethyl methacrylate (DMAEMA) from metalloinitiator 5 using a Cu(I)Br/N,N,N′,N′,N′-pentamethyldiethylenetriamine (PMDETA) or Cu(I)Br/1,1,4,7,10,10-hexamethyltriethylenetetramine (HMTETA) catalyst system to afford the PDMAEMA-g-[2Fe-2S]metallopolymer, as confirmed by IR spectroscopy (FIG. 10) and SEC in LiBr-DMF mobile phase (M.sub.n,SEC=9,500; M.sub.w/M.sub.n=1.33; (FIG. 9B). Hence, using this approach, a much higher local concentration of amine groups around the [2Fe-2S] core is created, since every DMAEMA repeating unit carries an amine side chain group, which could be precisely controlled by variation of the degree of polymerization as achieved by ATRP. PDMAEMA metallopolymers in the range of 10,000-15,000 g/mol with low dispersity were prepared and were water soluble, as well as soluble in ACN and DMF.

(74) For ATRP of DMAEMA using 5, a 10 mL Schlenk flask equipped with a Teflon-coated magnetic stir bar was added Cu(I)Br (2.55 mg, 0.0178 mmol), sealed with a rubber septum, evacuated and backfilled with Ar three times. Deoxygenated HMTETA (7.3 μL, 0.0267 mmol) was added to the flask followed by the addition of 0.2 mL of deoxygenated THF via purged syringe. The resulting mixture was stirred for 10 minutes to allow for the formation of the Cu-ligand complex. In a second 10 mL Schlenk flask equipped with a Teflon-coated magnetic stir bar, 5 (14.24 mg, 0.0178 mmol) was added. The flask was sealed with a rubber septum, evacuated and backfilled with Argon three times, and then purified and deoxygenated DMAEMA (0.30 mL, 1.78 mmol) was added via purged syringe, followed by the addition of 0.30 mL of deoxygenated, anhydrous THF. The solution was stirred until homogeneous then transferred to the reaction flask via purged syringe. The flask was placed in an oil bath at 50° C. and stirred for 90 min.

(75) Results

(76) Electrocatalytic CV experiments with PDMAEMA-g-[2Fe-2S] metallopolymers were performed in pH 7 neutral water. The PDMAEMA-g-[2Fe-2S] metallopolymer was catalytically active for H.sub.2 generation at low potentials (E.sub.onset=−0.85 V. E.sub.1/2=−1.05 V, and E.sub.ipc=−1.18 V, all aqueous potentials reported vs SHE), and modest metallopolymer loadings (1.6 mg/mL). Furthermore, the current densities generated by the PDMAEMA-g-[2Fe-2S] metallopolymer were comparable to that of a Pt electrode for H.sub.2 generation under identical conditions (FIG. 16).

(77) Air Stable Metallopolymers for HER.

(78) The oxygen sensitivity of PDMAEMA-g-[2Fe-2S] metallopolymers in aqueous media was investigated since it is known that one of the major challenges in developing robust [2Fe-2S] biomimetic catalysts is the poor oxygen stability of these complexes as also encountered in the [FeFe]-hydrogenase enzymes. Referring to FIG. 20, peak catalytic current, I.sub.pc1 was established for the sample under anaerobic conditions then the solution was bubbled with compressed air (21% O.sub.2) for 30 minutes. Cyclic voltammograms of the oxygenated solution showed a peak for O.sub.2 reduction (c.a. −0.4 V vs SHE) as well as a catalytic peak which retained 55% (±11%) of the peak catalytic current determined under anaerobic conditions. After storing the aerated solution in ambient conditions for 18 hours, the sample had slightly reduced activity compared with the previous day (39±7% of I.sub.pc) but sparging with argon for 30 minutes allowed for recovery of 90% (±2%) of I.sub.pc. Subsequently, a controlled potential Coulometry in a cyclic voltammetry cell was performed with no attempt to separate the catalytic solution from the O.sub.2 producing Pt counter electrode. No decay in current was observed over this time period, confirming the aerobic stability of the PDMAEMA-g-[2Fe-2S] system. This level of activity and stability in aerobic solutions is remarkable in light of the fact that oxygen sensitivity is one of the most persistent, unsolved problems plaguing [FeFe]—H.sub.2ase mimics.

(79) The previously described example demonstrated a versatile new methodology for the incorporation of catalytic moieties into metallopolymer frameworks. Using this new methodology, new metallopolymer systems were successfully synthesized, including PDMAEMA-g-[2Fe-2S], a water soluble HER catalyst that exhibits current densities comparable to a platinum electrode with an overpotential of only 0.23 V. This system has also demonstrated substantial aerobic stability. While the methodology has been demonstrated with vinylic monomers, the present invention is not limited to vinylic monomers alone. In other embodiments, this approach to active site polymer encapsulation may be utilized in a wide variety of catalytic systems to provide site isolation, solubility, improved stability, processability, and rate increases.

Alternative Catalyst Embodiments

(80) According to another embodiment, the present invention features a metallopolymer comprising photoactive regioregular poly(3-hexylthiophene) (P3HT) and catalytically active diiron-disulfide complexes. These diiron-based complexes are biomimetic analogues of the active sites in Fe—Fe hydrogenase enzymes that are also active in the electrocatalytic generation of molecular hydrogen (H.sub.2). As previously described, diiron-disulfide hexacarbonyl complexes (Fe.sub.2S.sub.2CO.sub.6) can be selectively functionalized to afford a variety of bonding motifs that readily lend themselves to the formation of metallopolymeric materials.

(81) Referring now to FIG. 21-31, the present invention features a photocatalytic metallopolymer composition for generating hydrogen (H.sub.2). In one embodiment, the composition may comprise a metallopolymer complex according to the following:

(82) ##STR00011##

(83) In some embodiments, R.sub.1 can be a polymeric ligand selected from a group consisting of a photoactive regioregular poly(3-hexylthiophene)(P3HT) ligand, a water soluble ligand, polyethylene oxide, poly(acrylic acid), and a polymer derived from monomers selected from a group consisting of vinylic monomers, ethylenically unsaturated monomers, styrenic monomers, acrylate monomers, methacrylate monomers, acrylonitrile monomers, allylic monomers, vinylpyridine monomers, isobutylene monomers, maleimide monomers, norbornene monomers, monomers having at least one vinyl ether moiety, monomers having at least one isopropenyl moiety, and alkynylly unsaturated monomers,

(84) In other embodiments, R.sub.2 may be selected from a group consisting of a phenyl, a

(85) ##STR00012##
with m ranging from 1 to 20, a

(86) ##STR00013##
where R.sub.3 is a phenyl or COOR.sub.4 and R.sub.4 is H or an alkyl group C.sub.2-C.sub.10, and a polymer derived from monomers selected from a group consisting of vinylic monomers, ethylenically unsaturated monomers, styrenic monomers, acrylate monomers, methacrylate monomers, acrylonitrile monomers, allylic monomers, vinylpyridine monomers, isobutylene monomers, maleimide monomers, norbornene monomers, monomers having at least one vinyl ether moiety, monomers having at least one isopropenyl moiety, and alkynylly unsaturated monomers. In a preferred embodiment, R.sub.2 can impart water solubility to the metallopolymer complex.

(87) Without wishing to limit the invention to a particular theory or mechanism, the polymeric ligand is capable of promoting photoinduced electron transfer to a diiron metal center of the metallopolymer complex. Further still, the metallopolymer complex generates Hz upon irradiation of the photocatalytic metallopolymer composition in the presence of a proton donor.

(88) According to another embodiment, the photocatalytic metallopolymer composition for generating hydrogen (Hz) may comprise a metallopolymer complex according to the following:

(89) ##STR00014##

(90) In one embodiment, L.sub.1 may be an aryl. In another embodiment, R.sub.1 and R.sub.2 can each be, independently, a —CO or a polymeric ligand capable of promoting photoinduced electron transfer to a diiron metal center of the metallopolymer complex. Examples of the polymeric ligand include, but are not limited to, a photoactive regioregular poly(3-hexylthiophene)(P3HT) ligand, a water soluble ligand, polyethylene oxide, poly(acrylic acid), and a polymer derived from monomers such as, for example, vinylic monomers, ethylenically unsaturated monomers, styrenic monomers, acrylate monomers, methacrylate monomers, acrylonitrile monomers, allylic monomers, vinylpyridine monomers, isobutylene monomers, maleimide monomers, norbornene monomers, monomers having at least one vinyl ether moiety, monomers having at least one isopropenyl moiety, or alkynylly unsaturated monomers. Preferably, upon irradiation of the photocatalytic metallopolymer composition in the presence of a proton donor, the metallopolymer complex generates Hz.

(91) In preferred embodiments, the polymeric ligand of any of the photocatalytic metallopolymer compositions described herein is a P3HT ligand. The P3HT ligand can act as a photosensitizer and intermolecular electron donor. In some embodiments, the P3HT ligand may be according to the following:

(92) ##STR00015##

(93) In some embodiments, n can range from 1 to 20. In other embodiments, R.sub.5 and R.sub.6 are each independently an H, an alkyl group C.sub.2-C.sub.10, or a phenyl.

(94) For any of the photocatalytic metallopolymer compositions described herein, the metallopolymer complex can absorb light in the UV-Visible spectrum. The metallopolymer complex may also be a biomimetic analogue of hydrogenase.

(95) According to one embodiment, the present invention features a method of generating molecular hydrogen (H.sub.2). The method may comprise providing any of the photocatalytic metallopolymer compositions, adding the photocatalytic metallopolymer composition to a proton source, and irradiating the photocatalytic metallopolymer composition and proton source with UV or visible light. Without wishing to limit the invention to a particular theory or mechanism, the photocatalytic metallopolymer composition can act as an electron donor upon irradiation with light, thereby reducing a proton of the proton source to produce H.sub.2. Examples of the proton source include, but are not limited to, water, a carboxylic acid, or a thiol.

(96) According to another embodiment, the present invention features a method of producing a photocatalytic metallopolymer complex for generating molecular hydrogen (H.sub.2). The method may comprise providing a diiron-disulfide complex according to the following structure:

(97) ##STR00016##

(98) In one embodiment, the method may further comprise providing poly(3-hexylthiophene)(P3HT), reacting the P3HT with an organometallic halide to produce a halide-terminated P3HT ligand, reacting the halide-terminated P3HT ligand with the diiron-disulfide complex such that the P3HT ligand binds to one of the sulphides, providing an alkyl halide-terminated polymer ligand, and alkylating the diiron-disulfide complex with the alkyl halide-terminated polymer ligand at the second sulfide to produce the photocatalytic metallopolymer complex. In some embodiments, the organometallic halide is MgX. In other embodiments, the alkyl halide-terminated polymer is benzyl chloride (BzCl), polystryrene BzCl (PS-BzCl), or poly(t-butyl acrylate)-BzCl)(PtBA-BzCl). Without wishing to limit the invention to a particular theory or mechanism, the P3HT ligand is capable of promoting photoinduced electron transfer to a diiron metal center of the metallopolymer complex. Upon irradiation of the metallopolymer complex in the presence of a proton donor, the metallopolymer complex generates H.sub.2.

(99) In yet another embodiment, the method of producing a photocatalytic metallopolymer complex for generating molecular hydrogen (H.sub.2) may comprise providing a diiron-disulfide complex according to the following structure:

(100) ##STR00017##
where L.sub.1 can be an aryl.

(101) In one embodiment, the method may further comprise providing poly(3-hexylthiophene)(P3HT), reacting P3HT with a phosphine to produce a phosphine-terminated P3HT ligand, and substituting at least one carbonyl moiety of the diiron-disulfide complex with the phosphine-terminated P3HT ligand to produce the photocatalytic metallopolymer complex. Without wishing to limit the invention to a particular theory or mechanism, the P3HT ligand is capable of promoting photoinduced electron transfer to a diiron metal center of the metallopolymer complex. The metallopolymer complex generates H.sub.2 upon irradiation of the metallopolymer complex in the presence of a proton donor.

(102) In some embodiments, a phosphine moiety of the phosphine-terminated P3HT ligand may comprise —PPh.sub.2. In other embodiments, one carbonyl moiety of the diiron-disulfide complex is substituted with the phosphine-terminated P3HT such that metallopolymer complex is unsymmetric. In yet other embodiments, two carbonyl moieties of the diiron-disulfide complex are each substituted with the phosphine-terminated P3HT such that metallopolymer complex is symmetric.

Photocatalyst Examples

(103) The following are non-limiting examples of the present invention. It is to be understood that said examples are provided for the purpose of demonstrating the present invention in practice, and is in no way intended to limit the invention. Equivalents or substitutes are within the scope of the invention.

Synthesis of P3HT Metallopolymers

(104) The synthesis of metallopolymers bearing a single P3HT ligand and a small molecule benzyl, or methyl group is shown in FIG. 23. A P3HT with a single terminal —MgX group is prepared via magnesium halogen exchange of a P3HT prepared by the GRIM method (which are capped with —H and —Br groups) followed by treatment with i-PrMgCl. Alkylation of the reactive thiolate form of the complex is conducted with benzyl halides, or methyl iodide. Structural characterization of the target metallopolymer may be determined using 1H NMR and IR spectroscopies in conjunction with SEC.

(105) Referring to FIG. 24, A-B diblock metallopolymers are prepared by alkylation of reactive P3HT thiolate intermediates with alkyl halide terminated polymers. The use of the benzyl chloride functional alkoxyamine initiators can afford well-defined homopolymers of polystyrene and polyacrylates bearing a primary benzyl chloride end group without the need for protecting group chemistry. Polystyrenes and poly(t-butyl acrylates) in the range of M.sub.n˜2000-5000 g/mol are prepared and used to form A-B diblock metallopolymer complexes, using the methods previously discussed. The efficiency of the alkylation reaction can be quantified using SEC. Purification of the metallopolymer can be conducted using silica gel column chromatography, which is effective to remove more polar polyacrylates.

(106) Furthermore, water soluble A-B diblock metallopolymers can be prepared via alkylation of alkyl halide terminated methyl monoether polyethylene glycol (M.sub.n˜2000-10000 g/mol) with P3HT thiolate intermediates. Water soluble complexes can also be prepared by acidic deprotection of P3HT-block-Fe.sub.2S.sub.2(CO).sub.6-block-poly(acrylic acid) (P3HT-b-Fe.sub.2S.sub.2CO.sub.6-b-PAA) with TFA, since the diiron complex was found to be stable to TFA. Without wishing to limit the invention to a particular theory or mechanism, the amphiphilic A-B diblock metallopolymers can form block copolymer micelles when dispersed in water.

(107) Phosphine Terminated P3HT Ligands.

(108) Referring to FIG. 25, an additional strategy for preparing P3HT covalently attached to a [FeFe]-hydrogenase active site mimic is to append P3HT with a phosphine moiety which can then be used as a ligand for iron in place of a CO ligand. The simplest strategy for accomplishing this is to prepare P3HT with a terminal phosphine ligand. In a few cases, the metal complexes can be electropolymerized to give conducting films but the preparation of polythiophenes appended with phosphines and their metal complexes have not been reported. Consequently, the first task is to prepare P3HT with a terminal phosphine. The standard method for preparing thiophene phosphines is to react a lithiothiophene with a phosphorus electrophile: Ar.sub.2PX, ArPX.sub.2 or PX.sub.3, X═Cl or Br. The lithiothiophene is obtained by deprotonation of the thiophene with t-BuLi or halogen metal exchange of the α-halo (Br or I) thiophene with n-BuLi. Once the phosphine terminated P3HT is in hand the reactions with Benzcat is carried analogously to the ligand substitution reactions. The ability of phosphine terminated P3HT ligated to Benzcat to generate H.sub.2 on irradiation can be evaluated using the methodology outlined above for the other P3HT-[2Fe2S] polymers. Without wishing to limit the invention to a particular theory or mechanism, the [FeFe]-hydrogenase active site mimics with phosphines instead of CO ligands are reduced at potentials 0.2 to 0.3 V more negative. This means that the LUMO energy level of these complexes is raised and the viability of electron-transfer from the excited state HOMO of the P3HT moiety to the [2Fe2S] moiety may be at issue. However, the electron donating ability of the phosphine may be ameliorated by electron-withdrawing substituents; thus, metallopolymers can also be prepared from the commercially available bis(p-trifluoromethylphenyl)phosphorus chloride and bis(p-pentafluoro-phenyl)phosphorus chloride. In addition, pyrrolidino groups on phosphorus increase their n-acceptor properties and it has been reported that the mono- and bis-tripyrrolidinophosphine complexes undergo only small cathodic shifts of 30 and 60 mV, respectively, as compared to their all-CO ligated [2Fe2S] complexes.

(109) Characterization of Metallopolymers

(110) Various spectroscopic methods such as .sup.1H and .sup.13C NMR and IR are useful in characterizing 2Fe2S active site mimics as well as X-ray crystallography. X-ray crystal structure analysis is not feasible for the metallopolymers but NMR and IR spectroscopic analysis are essential. In addition, to .sup.1H and .sup.13C NMR spectroscopic analysis .sup.31P NMR spectroscopy are useful in characterizing the phosphino polymeric ligands and their 2Fe2S complexes. It should be noted that IR spectroscopic analysis is especially useful because the metal carbonyl stretching bands are especially strong and occur in a characteristic region of the IR that is devoid of most other absorptions. In addition, the position of these bands depends on the electron richness of the metal center, for example, the metal carbonyl IR stretching frequencies of 1PTA occur at 2052 (s), 1993 (s), 1978 (s), 1939 (w) whereas those of the more electron-rich center in the bis-phosphine complex 1PTA2 occur at 2002 (s), 1959 (s), 1936 (s), 1926 (w) cm.sup.−1. In the case of P3HT, the hexyl groups and thiophene hydrogens occur in characteristic regions and it is known that in thiol terminated P3HT the chemical shift of the adjacent CH.sub.2 moiety of the hexyl group undergoes a shift.

(111) Intermolecular Electron Transfer

(112) In one embodiment, poly(3-hexylthiophene) (P3HT) and fullerene derivatives are used in bulk heterojunction solar cells because upon irradiation, P3HT forms excitons which migrate to the interface with the fullerene derivative wherein ionization occurs with an electron migrating through the fullerene and the hole migrating through the P3HT. To effect exciton dissociation, a key advance was the finding that photoinduced electron-transfer from π-conjugated polymers such as polythiophene to C.sub.60 was ultrafast. Consequently, bulk heterojunction cells, epitomized by regioregular poly(3-hexylthiophene) P3HT and a fullerene derivative: [6,6]-phenyl-C.sub.61 butyric acid methyl ester C.sub.61PCBM, in which the two materials form a interpenetrating bi-continuous material proved especially advantageous. Here, on photoexcitation, the exciton formed in the P3HT material diffuses to the interface with C.sub.61PCBM and an electron is transferred. In this process, the photoexcited P3HT acts as an electron donor and the C.sub.61PCBM acts as an electron acceptor. Although this electron transfer separates the electron and hole, they are still coulombically bound. This coulombically bound interfacial electron-hole pair must then dissociate into free charge carriers.

(113) The fullerene derivative can be replaced by a bioinspired hydrogenase active site 2Fe-2S model and covalently linked. Furthermore, the experiments can be done in solution in the presence of weak acid that is stronger than acetic acid, and a sacrificial electron donor. It is expected that the polythiophene preferentially absorbs the light. Without wishing to limit the invention to a particular theory or mechanism, the exciton formed by absorption of a photon by P3HT would ionize and transfer an electron to Benzcat forming the corresponding radical anion and concomitantly forming a hole in the polymer. For this to be energetically favorable, the LUMO energy level of the P3HT must be higher in energy than the LUMO level of Benzcat. Furthermore, the reduction of potential of Benzcat and its LUMO energy can be tuned by substituents on the benzene ring. In order to generate H.sub.2 from protons, 2e.sup.− are required as follows: 2H.sup.++2e.sup.−=H.sub.2.

(114) Addition of a second electron to Benzcat is more favorable energetically than addition of the first electron, that is, there is potential inversion, rendering addition of a second electron to the stable Benzcat anion radical more favorable than the first after reorganization as outlined in FIG. 26. Note that the reorganization obtained after one-electron reduction requires rotation around one of the Fe atoms, formation of a bridging CO and Fe—S bond weakening. Protonation followed by H.sub.2 loss regenerates Benzcat. The hole in P3HT is filled by the sacrificial electron donor regenerating P3HT.

(115) An experiment was done in which a solution of P3HT and Benzcat in toluene was irradiated with light of greater than 450 nm with thiophenol as the proton and electron source and the formation of H.sub.2 was detected by gas chromatographic analysis on a molecular sieves column using a thermal conductivity detector. Efficient photocatalytic generation of H.sub.2 was shown by GC analysis (see FIG. 28). It is theorized that the mechanism occurs in which 2e are added to Benzcat and thiophenol protonates the dianion. The hole in the P3HT is filled by electron transfer from thiophenol and this generates strong acid to react with the μ-bridged hydride producing H.sub.2 and regenerating Benzcat. It should be noted that spectroscopic studies with P3HT and Benzcat did not show any evidence for association in the ground state, that is, the UV-Vis absorption spectrum of a mixture of P3HT and Benzcat was the same as the sum of the individual spectra. In this experiment, the photoexcited P3HT and Benzcat must near each other for electron transfer to occur. In other embodiments, it may be possible to improve this electron transfer by covalently attaching the two moieties by side-chain or end functionalization of P3HT.

(116) Intramolecular Electron Transfer

(117) The efficiency of electron transfer between P3HT and Fe2S2 catalytic moieties on irradiation can increase in the metallopolymers outlined above. Consequently, irradiation of these metallopolymers in organic solvents in the presence of thiophenol can more efficiently produce H.sub.2. In addition, irradiation of the A-B diblock metallopolymers can be done in water or aqueous THF. Without wishing to limit the invention to a particular theory or mechanism, it is theorized that this reaction is a surface reaction in which the thiolate anion binds to the surface of the quantum dot and transfers an electron to the photoexcited quantum dot. The thiolate radical, which is observed by EPR spectroscopy, then couples and concomitantly forms H.sub.2. However, no H.sub.2 is produced upon irradiation of P3HT and thiophenol. The presence of Benzcat is required for rapid production of H.sub.2. It is important to note that the present experiments were done in toluene. Under aqueous conditions, thiolate is present, but in toluene, its concentration is very low because the pKa of thiophenol in toluene is much greater than in water. It should be emphasized that under the present conditions, it is assumed that the reaction forming H.sub.2 is ionic, not free radical. That is, a proton reacts with the iron hydride forming H.sub.2. The consequences of performing the photoreaction with 2Fe2S metallopolymers in water are of value. It should be noted that irradiation of Benzcat in the presence of eosin as photosensitizer and Et.sub.3N as sacrificial electron donor at pH<6 in SDS micelles affords H.sub.2. For example, the aqueous system allows for control of the pH of the solution using buffers. Irradiation of P3HT-2Fe2S in the presence of thiophenol at neutral pH may result in evolution of H.sub.2 due to the free radical process outlined above owing to the presence of phenylthiolate. However, at low pH where there is little thiolate, the ionic mechanism outlined above may dominate. This is important because in water, splitting cell protons generated by oxidation of water can catalytically reduce on irradiation of the present catalysts. In the system in which hydrogenase is replaced by P3HT-2Fe2S photocatalysts, both the oxidation of water and the reduction of protons would be photocatalyzed. Ideally, in such a system no sacrificial reagent would be required.

(118) [FeFe]-Hydrogenase mimics absorb in the visible in the same region as polythiophenes. Consequently, it is relevant to consider which moiety preferentially absorbs light. Oligothiophenes may be able to selectively absorb light and there may even be charge transfer bands in these complexes. Of particular note is the visible absorption spectrum of terthiophene catalyst as compared with monothiophene catalyst, as shown in FIG. 31. The extinction coefficient for the absorption at ca. 350 nm increases dramatically as the number of thiophene rings increases. Furthermore, there appears to be long wavelength bands in the oligothiophene complexes that are not in the monothiophene complex. In the visible absorption spectrum of the terthiophene catalyst, there is a new peak with a maximum 90 nm to the pentane line of the monothiophene complex and the extinction coefficient is increased dramatically (ca. 25×). This long wavelength band suggests the possibility of a charge transfer band with the oligothiophene acting as the donor and the Fe2S2 moiety acting as the acceptor. Although the new long wavelength bands do not shift in absorption maxima as a function of solvent polarity, they still may be charge transfer bands.

(119) As used herein, the term “about” refers to plus or minus 10% of the referenced number.

(120) Various modifications of the invention, in addition to those described herein, will be apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. Each reference cited in the present application is incorporated herein by reference in its entirety.

(121) Although there has been shown and described the preferred embodiment of the present invention, it will be readily apparent to those skilled in the art that modifications may be made thereto which do not exceed the scope of the appended claims. Therefore, the scope of the invention is only to be limited by the following claims. In some embodiments, the figures presented in this patent application are drawn to scale, including the angles, ratios of dimensions, etc. In some embodiments, the figures are representative only and the claims are not limited by the dimensions of the figures. In some embodiments, descriptions of the inventions described herein using the phrase “comprising” includes embodiments that could be described as “consisting of”, and as such the written description requirement for claiming one or more embodiments of the present invention using the phrase “consisting of” is met.