Cobalt Precatalysts Research Articles

Kinetic and thermodynamic control of C(sp2)-H activation enables site-selective borylation.

Catalysts that distinguish between electronically distinct carbon-hydrogen (C-H) bonds without relying on steric effects or directing groups are challenging to design. In this work, cobalt precatalysts supported by N-alkyl-imidazole-substituted pyridine dicarbene (ACNC) pincer ligands are described that enable undirected, remote borylation of fluoroaromatics and expansion of scope to include electron-rich arenes, pyridines, and tri- and difluoromethoxylated arenes, thereby addressing one of the major limitations of first-row transition metal C-H functionalization catalysts. Mechanistic studies established a kinetic preference for C-H bond activation at the meta-position despite cobalt-aryl complexes resulting from ortho C-H activation being thermodynamically preferred. Switchable site selectivity in C-H borylation as a function of the boron reagent was thereby preliminarily demonstrated using a single precatalyst.

Phenoxythiazoline (FTz)‐Cobalt(II) Precatalysts Enable C(sp2)–C(sp3) Bond‐Formation for Key Intermediates in the Synthesis of Toll‐like Receptor 7/8 Antagonists**

AbstractEvaluation of the relative rates of the cobalt‐catalyzed C(sp2)–C(sp3) Suzuki–Miyaura cross‐coupling between the neopentylglycol ester of 4‐fluorophenylboronic acid and N‐Boc‐4‐bromopiperidine established that smaller N‐alkyl substituents on the phenoxyimine (FI) supporting ligand accelerated the overall rate of the reaction. This trend inspired the design of optimal cobalt catalysts with phenoxyoxazoline (FOx) and phenoxythiazoline (FTz) ligands. An air‐stable cobalt(II) precatalyst, (FTz)CoBr(py)3 was synthesized and applied to the cross‐coupling of an indole‐5‐boronic ester nucleophile with a piperidine‐4‐bromide electrophile that is relevant to the synthesis of reported toll‐like receptor (TLR) 7/8 antagonist molecules including afimetoran. Addition of excess KOMe⋅B(OiPr)3 improved catalyst lifetime due to attenuation of alkoxide basicity that otherwise resulted in demetallation of the FI chelate. A first‐order dependence on the cobalt precatalyst and a saturation regime in nucleophile were observed, supporting turnover‐limiting transmetalation and the origin of the observed trends in N‐imine substitution.

Phenoxythiazoline (FTz)-Cobalt(II) Precatalysts Enable C(sp2 )-C(sp3 ) Bond-Formation for Key Intermediates in the Synthesis of Toll-like Receptor 7/8 Antagonists.

Evaluation of the relative rates of the cobalt-catalyzed C(sp2 )-C(sp3 ) Suzuki-Miyaura cross-coupling between the neopentylglycol ester of 4-fluorophenylboronic acid and N-Boc-4-bromopiperidine established that smaller N-alkyl substituents on the phenoxyimine (FI) supporting ligand accelerated the overall rate of the reaction. This trend inspired the design of optimal cobalt catalysts with phenoxyoxazoline (FOx) and phenoxythiazoline (FTz) ligands. An air-stable cobalt(II) precatalyst, (FTz)CoBr(py)3 was synthesized and applied to the cross-coupling of an indole-5-boronic ester nucleophile with a piperidine-4-bromide electrophile that is relevant to the synthesis of reported toll-like receptor (TLR) 7/8 antagonist molecules including afimetoran. Addition of excess KOMe⋅B(Oi Pr)3 improved catalyst lifetime due to attenuation of alkoxide basicity that otherwise resulted in demetallation of the FI chelate. A first-order dependence on the cobalt precatalyst and a saturation regime in nucleophile were observed, supporting turnover-limiting transmetalation and the origin of the observed trends in N-imine substitution.

Unveiling the Structural Self-Reconstruction and Identifying the Reactive Center of a V, Fe Co-Doped Cobalt Precatalyst toward Enhanced Overall Water Splitting by Operando Raman Spectroscopy.

The development of efficient and stable bifunctional electrocatalysts based on non-noble metals for water electrolysis is both urgent and challenging. However, unresolved issues remain regarding the challenge of identifying the active phase and gaining a comprehensive understanding of its surface reconstruction and functionality throughout the reaction process. In this study, we have combined doping and heterostructure construction by a one-step electrodeposition and a subsequent activation treatment to synthesize Fe, V co-doped Co3O4/Co(OH)2 and Co/Co(OH)2 heterointerfaces (referred to as A-Co60Fe1.1V). These heterointerfaces, composed of Co/Co(OH)2 and Co3O4/Co(OH)2, are proposed to facilitate charge transfer process during catalysis. X-ray photoelectron spectroscopy (XPS) analysis demonstrates that the introduction of V and Fe dopants increases the valence state of Co centers in Co3O4 and Co(OH)2. Further operando Raman spectroscopy reveals that Co(OH)2 and Co3O4 with the high-valence Co centers remain stable during the hydrogen evolution reaction (HER) process. These high-valence Co centers are believed to promote the crucial water dissociation step and therefore enhance the overall HER catalysis. On the other hand, during the oxygen evolution reaction (OER), Fe, V co-doping leads to an earlier formation of the active CoOOH species, while Fe doping can further help stabilize the more reactive β-CoOOH species instead of the less reactive γ-CoOOH. As a result, the A-Co60Fe1.1V catalyst exhibits significantly improved catalytic activity for both HER and OER that it requires low overpotentials of 51 and 250 mV, respectively, to attain a current density of 10 mA cm-2. Moreover, when utilized as both the cathode and anode in alkaline water electrolysis, the A-Co60Fe1.1V catalyst can operate at a mere 1.54 V voltage while maintaining 10 mA cm-2, surpassing the majority of non-noble metal catalysts. Remarkably, it also exhibits stability for at least 40 h at ∼100 mA cm-2.

Vitamin B12 Derivative Enables Cobalt-Catalyzed Atom Transfer Radical Polymerization.

Advances in controlled radical polymerizations by cobalt complexes have primarily taken advantage of the reactivity of cobalt as a persistent radical to reversibly deactivate propagating chains by forming a carbon-cobalt bond. However, cobalt-mediated radical polymerizations require stoichiometric ratios of a cobalt complex, deterring its utility in synthesizing well-defined polymers. Here, we developed a strategy to use cobalt as a catalyst to control radical polymerizations via halogen atom transfer with alkyl halide initiators. Using a modified, hydrophobic analogue of vitamin B12 (heptamethyl ester cobyrinate) as a cobalt precatalyst, we controlled the polymerization of acrylate monomers. The polymerization efficiency of the cobalt catalyst was significantly improved by additional bromide anions, which enhanced the deactivation of propagating radicals yielding polymers with dispersity values <1.2 using catalyst concentrations as low as 5 mol %. We anticipate that the development of cobalt catalysis in atom transfer radical polymerization will enable new opportunities in designing catalytic systems for the controlled synthesis of polymers.

Mechanistic Investigations of Phenoxyimine-Cobalt(II)-Catalyzed C(sp2)-C(sp3) Suzuki-Miyaura Cross-Coupling.

The mechanism of phenoxyimine (FI)-cobalt-catalyzed C(sp2)-C(sp3) Suzuki-Miyaura cross-coupling was studied using a combination of kinetic measurements and catalytic and stoichiometric experiments. A series of dimeric (FI)cobalt(II) bromide complexes, [(4-CF3PhFI)CoBr]2, [(4-OMePhFI)CoBr]2, and [(2,6-diiPrPhFI)CoBr]2, were isolated and characterized by 1H and 19F NMR spectroscopies, solution and solid-state magnetic susceptibility, electron paramagnetic resonance (EPR) spectroscopy, X-ray crystallography, and diffusion-ordered NMR spectroscopy (DOSY). One complex, [(4-CF3PhFI)CoBr]2, was explored as a single-component precatalyst for C(sp2)-C(sp3) Suzuki-Miyaura cross-coupling. Addition of potassium methoxide to [(4-CF3PhFI)CoBr]2 generated the corresponding (FI)cobalt(II) methoxide complex as determined by 1H and 19F NMR and EPR spectroscopies. These spectroscopic signatures were used to identify this compound as the resting state during catalytic C(sp2)-C(sp3) coupling. Variable time normalization analysis (VTNA) of in situ catalytic 19F NMR spectroscopic data was used to establish an experimental rate law that was first-order in a (FI)cobalt(II) precatalyst, zeroth-order in the alkyl halide, and first-order in an activated potassium methoxide-aryl boronate complex. These findings are consistent with turnover-limiting transmetalation that occurs prior to activation of the alkyl bromide electrophile. The involvement of boronate intermediates in transmetalation was corroborated by Hammett studies of electronically differentiated aryl boronic esters. Together, a cobalt(II)/cobalt(III) catalytic cycle was proposed that proceeds through a "boronate"-type mechanism.

Asymmetric Hydrogenation of Indazole-Containing Enamides Relevant to the Synthesis of Zavegepant Using Neutral and Cationic Cobalt Precatalysts.

The cobalt-catalyzed asymmetric hydrogenation of indazole-containing enamides relevant to the synthesis of the calcitonin gene-related peptide (CGRP) receptor antagonist, zavegepant (1), approved for the treatment of migraines, is described. Both neutral bis(phosphine)cobalt(II) and cationic bis(phosphine)cobalt(I) complexes served as efficient precatalysts for the enamide hydrogenation reactions, providing excellent yield and enantioselectivities (up to >99.9%) for a range of related substrates, though key reactivity differences were observed. Hydrogenation of indazole-containing enamide, methyl (Z)-2-acetamido-3-(7-methyl-1H-indazol-5-yl)acrylate, was performed on a 20 g scale.

Ultrahigh activity and broad temperature resistance of amine-imine cobalt precatalysts for butadiene polymerization.

A series of amine-imine cobalt complexes (Co1-Co7) has been prepared and characterized. The complexes Co3, Co4, and Co6 have a distorted tetrahedral geometry, as determined by single crystal X-ray diffraction. In the presence of ethylaluminum sesquichloride (EASC), Co3 exhibited ultra-high activity toward butadiene (Bd) polymerization (up to 7813 kgpolymer mol-1 h-1). The activity is higher than any yet recorded for which yield high cis-1,4 polybutadiene by the well-defined late-transition metal catalytic system. The catalyst also exhibited excellent tolerance towards the ratio of Co/Bd and broad temperature stability. At a ratio of Bd/Co3 = 50 000, the complexes Co1-3 can afford polybutadiene with yields higher than 96% within 2 hours. At -20 °C to 100 °C, the complex Co3 afforded relatively high polymer yields at low catalyst concentrations (Bd/Co3 = 25 000). In addition, all polymers showed a relatively high molecular weight (up to 1.06 × 106 g mol-1).

Mechanistic Investigations of the Asymmetric Hydrogenation of Enamides with Neutral Bis(phosphine) Cobalt Precatalysts.

The mechanism of the asymmetric hydrogenation of prochiral enamides by well-defined, neutral bis(phosphine) cobalt(0) and cobalt(II) precatalysts has been explored using(R,R)-iPrDuPhos ((R,R)-iPrDuPhos = (+)-1,2-bis[(2R,5R)-2,5-diisopropylphospholano]benzene) as a representative chiral bis(phosphine) ligand. A series of (R,R)-(iPrDuPhos)Co(enamide) (enamide = methyl-2-acetamidoacrylate (MAA), methyl(Z)-α-acetamidocinnamate (MAC), and methyl(Z)-acetamido(4-fluorophenyl)acrylate (4FMAC)) complexes (1-MAA, 1-MAC, and 1-4FMAC), as well as a dinuclear cobalt tetrahydride, [(R,R)-(iPrDuPhos)Co]2(μ2-H)3(H) (2), were independently synthesized, characterized, and evaluated in both stoichiometric and catalytic hydrogenation reactions. Characterization of (R,R)-(iPrDuPhos)Co(enamide) complexes by X-ray diffraction established the formation of the pro-(R) diastereomers in contrast to the (S)-alkane products obtained from the catalytic reaction. In situ monitoring of the cobalt-catalyzed hydrogenation reactions by UV-visible and freeze-quench electron paramagnetic resonance spectroscopies revealed (R,R)-(iPrDuPhos)Co(enamide) complexes as the catalyst resting state for all the three enamides studied. Variable time normalization analysis kinetic studies of the cobalt-catalyzed hydrogenation reactions in methanol established a rate law that is first order in (R,R)-(iPrDuPhos)Co(enamide) and H2 but independent of the enamide concentration. Deuterium-labeling studies, including measurement of an H2/D2 kinetic isotope effect and catalytic hydrogenations with HD, established an irreversible H2 addition step to the bound enamide. Density functional theory calculations support that this step is both rate and selectivity determining. Calculations, as well as HD-labeling studies, provide evidence for two-electron redox cycling involving cobalt(0) and cobalt(II) intermediates during the catalytic cycle. Taken together, these experiments support an unsaturated pathway for the [(R,R)-(iPrDuPhos)Co]-catalyzed hydrogenation of prochiral enamides.

Selectivity diversity for a single cobalt(II) precatalyst mediated butadiene polymerization

Selectivity diversity from a single catalyst not only allows for facile switch the type of product, but also helps to understand the reaction mechanism by simply varying the reaction conditions. In this research, we disclosed the capability of diversified selectivity of a cobalt complex as precatalyst to mediated 1,3-butadiene, which could produce different structures polymers under different conditions. On direct activation by EASC or MAO, such a complex was able to reveal high cis-1,4- selectivity, giving polybutadiene (PB) products with extremely low glass transition temperature; introducing PPh3 as external donor to such a system, the selectivity could switch from cis-1,4- to highly 1,2- manner, giving atactic 1,2- PBs. Moreover, the 1,2- contents of the obtained polymers were proportionally dependent on the PPh3 equivalents, gradual increasing PPh3/Co ratio was able to access cis-1,4-ran-1,2- products with gradual increased 1,2-contents. In contrast, selecting CS2 as donor could give high syndiotactic 1,2-PB products, which demonstrated melting temperatures up to 203.9 °C. Possible mechanism for such a selectivity diversity was proposed.

Development of Cobalt Catalysts for the meta-Selective C(sp2)-H Borylation of Fluorinated Arenes.

Cobalt precatalysts for the meta-selective borylation of fluorinated arenes are described. Initial screening and stoichiometric reactivity studies culminated in the preparation of a cobalt alkyl precatalyst supported by the sterically protected terpyridine (5,5″-Me2ArTpy = 4'-(4-N,N'-dimethylaminophenyl)-5,5″-dimethyl-2,2':6',2″-terpyridine). Under the optimized conditions, borylation with this precatalyst afforded up to 16 turnovers and near-exclusive meta regioselectivity with a range of substituted fluoroarenes in cyclopentyl methyl ether solvent at room temperature. Deuterium kinetic isotope effects of 2.9(2) at 23 °C support a turnover-limiting and selectivity-determining C(sp2)-H activation step, and stoichiometric C-H activation experiments provided insights into the identity of the C-H activating intermediate in catalysis. Analysis of the relevant Co-C and C-H bond thermodynamics support that the thermodynamics of C-H activation favor ortho-to-fluorine selectivity, providing additional, indirect support for kinetic control of C-H activation as the origin of meta selectivity.

Cobalt-Catalyzed C(sp2)-C(sp3) Suzuki-Miyaura Cross-Coupling Enabled by Well-Defined Precatalysts with L,X-Type Ligands.

Cobalt(II) halides in combination with phenoxy-imine (FI) ligands generated efficient precatalysts in situ for the C(sp2)-C(sp3) Suzuki-Miyaura cross coupling between alkyl bromides and neopentylglycol (hetero)arylboronic esters. The protocol enabled efficient C-C bond formation with a host of nucleophiles and electrophiles (36 examples, 34-95%) with precatalyst loadings of 5 mol%. Studies with alkyl halide electrophiles that function as radical clocks support the intermediacy of alkyl radicals during the course of the catalytic reaction. The improved performance of the FI-cobalt catalyst was correlated with decreased lifetimes of cage-escaped radicals as compared to diamine-type ligands. Studies of the phenoxy(imine)-cobalt coordination chemistry validate the L,X interaction leading to the discovery of an optimal, well defined, air-stable mono-FI cobalt(II) precatalyst structure.

Hydroboration of isocyanates: cobalt-catalyzed vs. catalyst-free approaches.

Hydroboration of isocyanates with HBPin was demonstrated using both catalytic and catalyst-free approaches. In arene solvents, the reactions employed the commercially available and bench-stable Co(acac)2/dpephos (dpephos = bis[(2-diphenylphosphino)phenyl] ether) pre-catalyst and proved chemodivergent, showing the formation of either formamides or N-methylamines, depending on the concentration of HBPin and the reaction conditions used. Catalytic monohydroboration of isocyanates to formamides was found to be highly chemoselective, tolerating alkenes, alkynes, aryl halides, esters, carboxamides, nitriles, nitroarenes and heteroaromatic functionalities. The catalyst-free hydroboration reactions have been demonstrated in neat HBPin. Whereas monohydroboration proved less selective compared with Co(acac)2/dpephos-catalyzed transformations, selective deoxygenative hydroboration of isocyanates to N-methylamines was observed under catalyst-free conditions.

4,4′-Dimethoxybenzhydryl substituent augments performance of bis(imino)pyridine cobalt-based catalysts in ethylene polymerization

A series of cobalt complexes with bis(imino)pyridine derivatives featuring unsymmetrical substitution with bulky groups has been synthesized and characterized. The molecular structures of two representatives have been determined by the single-crystal X-ray diffraction study, revealing distorted tetrahedral geometry with different degrees of steric hindrance imparted by the two inequivalent aryl groups attached to the imine nitrogen atoms. On activation with either MAO or MMAO, these complexes display high activity toward ethylene polymerization, reaching 8.71 × 106 g of PE (mol of Co)−1 h−1 at 60 °C and produce polyethylene of high molecular weight (Mw = 5.27 × 105 g mol−1) and low dispersity. The presence of the methoxy-substituent noticeably enhances the activity of the cobalt catalyst and increases the molecular weight of the resultant polyethylene.

Effect of Pincer Methylation on the Selectivity and Activity in (PNP)Cobalt-Catalyzed C(sp2)-H Borylation.

Cobalt complexes supported by a tetramethylated PNP pincer ligand (Me4 iPrPNP = 2,6-(iPr2PCMe2)2(C5H3N)) have been synthesized and structurally characterized. Examples include cobalt(I)-choride, -methyl, -aryl and -benzofuranyl derivatives. The performance of these compounds was evaluated in the catalytic borylation of fluorinated arenes using B2Pin2 as the boron source. While P-C bond cleavage, a known deactivation pathway in [(PNP)Co]-catalyzed borylation was suppressed, the overall activity and selectivity of the borylation of fluoroarenes was reduced as compared to the previously reported [(PNP)Co] catalyst lacking isopropylene spacers. Stoichiometric reactions support an increased barrier for oxidative addition to cobalt(I), a result of the increased steric profile and decreased conformational flexibility of the pincer resulting from methylation distal to the active site. With a more activated substrate such as benzofuran, catalytic borylation with cobalt(I) precatalysts and HBPin was observed. Monitoring the progress of the reaction by NMR spectroscopy revealed the presence of cobalt(III) intermediates during the course of the borylation, supporting a cobalt(I)-(III) redox cycle.

Catalytic Hydrogenation of Alkenes and Alkynes by a Cobalt Pincer Complex: Evidence of Roles for Both Co(I) and Co(II)

The Co(I) complex, [Co(N2)(CyPNP)] (CyPNP = anion of 2,5-bis-(dicyclohexylphosphinomethyl)pyrrole), is active toward the catalytic hydrogenation of terminal alkenes and the semi-hydrogenation of internal alkynes under 2 bar of H2 (g) at room temperature. The products of alkyne semi-hydrogenation are a mixture of E- and Z-alkenes. By contrast, use of the related cobalt(I) precatalyst, [Co(PMe3)(CyPNP)], results in formation of exclusively Z-alkenes. A semi-stable Co(II) species, [CoH(CyPNP)], can also be generated by treatment of degassed solutions of [Co(N2)(CyPNP)] with H2. The CoII-hydride displays activity toward both alkene hydrogenation and isomerization, but its instability hampers implementation as a catalyst. Several species relevant to potential catalytic intermediates have been isolated and detected in solution. These compounds include alkene and alkyne adducts of Co(I) as well as a Co(III) dihydride species. Catalytic results with the compounds examined are most consistent with a process involving shuttling between Co(I) and Co(III) states. However, generation of small quantities of Co(II) during catalytic turnover appears to be responsible for the isomerization observed for alkyne semi-hydrogenation. The interplay of cobalt oxidation states within the same catalyst system is discussed in the context of mechanistic scenarios for catalytic hydrogenation.

Rational Design of Cycloheptyl‐Fused Bis(arylimino)pyridyl‐cobalt(II) Precatalysts Adorned with Sterically and Electronically Modified N‐Aryls for Enhancing Ethylene Polymerization

AbstractThe sterically and electronically modified cycloheptyl‐fused bis(arylimino)pyridine‐cobalt(II) chloride precatalysts [2,3 : 5,6‐{C4H8C(N‐2,4‐(C15H13)‐6‐R‐C6H2}2C5HN]CoCl2 (R=Me (Co1), Et (Co2), i‐Pr (Co3), Cl (Co4), and F (Co5)) have been prepared via one‐pot synthesis approach. All the precatalysts were characterized by elemental analysis, FT‐IR spectroscopy and the single‐crystal X‐ray diffraction for Co2 confirmed distorted‐square‐pyramidal geometry around the cobalt center. On activation with either MAO (methylaluminoxane) or MMAO (modified methylaluminoxane), all the cobalt precatalysts displayed high catalytic activities for ethylene polymerization with peak performance of 3.47×106 g (PE) mol−1 (Co) h−1 at 50 °C using MAO and 4.53×106 g (PE) mol−1 (Co) h−1 at 30 °C with MMAO. The steric and electronic influence of the ortho‐substitutions (R) displayed significant effect on the catalytic activity and molecular weight of the resultant polyethylene. Notably, the precatalyst Co5 (R=F) exhibited high activity, delivering high‐molecular‐weight (558.17 kg mol−1) polyethylene; highlights the beneficial effect of ortho‐substituents (R) alongside with dibenzocycloheptyl groups. In addition, analysis of the obtained polyethylene showed strictly linear structure with saturated and unsaturated (vinyl) end groups.

Enhancing Ethylene Polymerization of NNN-Cobalt(II) Precatalysts Adorned with a Fluoro-substituent

Unsymmetrical 2-(1-(2,4-dibenzhydryl-6-fluorophenylimino)ethyl)-6-(1-alkylphenyl-imino)ethyl)pyridine compounds (Ar = 2,6-Me2C6H3 in L1; 2,6-Et2C6H3 in L2; 2,6-iPr2C6H3 in L3; 2,4,6-Me3C6H2 in L4; 2,6-Et2-4-Me-C6H2 in L5) were prepared and characterized. The treatment of CoCl2 with the compounds L1–L5 afforded the corresponding cobalt complexes Co1–Co5 in excellent yields. The molecular structures of Co3 and Co4 were determined by single-crystal X-ray diffraction, revealing the distorted-square-pyramidal geometry with three nitrogen atoms and two chlorine atoms around the cobalt center. Compared with previous bis(imino)pyridylcobalt analogues, all of the cobalt precatalysts displayed exceptionally higher activities toward ethylene polymerization with 1.32 × 107 g (PE) mol–1 (Co) h–1 at 60 °C in the presence of a co-catalyst MAO or MMAO. These cobalt catalysts produced highly linear polyethylene (PE) waxes with vinyl end groups and low molecular weight (Mw up to 8.23 kg mol–1) along with a relatively lower melting point (all-round Tms < 128 °C). The narrow dispersity of resultant polyethylenes indicated the single-site active species of the catalytic system.

Visible-Light-Enhanced Cobalt-Catalyzed Hydrogenation: Switchable Catalysis Enabled by Divergence between Thermal and Photochemical Pathways

The catalytic hydrogenation activity of the readily prepared, coordinatively saturated cobalt(I) precatalyst, (R,R)-(iPrDuPhos)Co(CO)2H ((R,R)-iPrDuPhos = (+)-1,2-bis[(2R,5R)-2,5-diisopropylphospholano]benzene), is described. While efficient turnover was observed with a range of alkenes upon heating to 100 °C, the catalytic performance of the cobalt catalyst was markedly enhanced upon irradiation with blue light at 35 °C. This improved reactivity enabled hydrogenation of terminal, di-, and trisubstituted alkenes, alkynes, and carbonyl compounds. A combination of deuterium labeling studies, hydrogenation of alkenes containing radical clocks, and experiments probing relative rates supports a hydrogen atom transfer pathway under thermal conditions that is enabled by a relatively weak cobalt–hydrogen bond of 54 kcal/mol. In contrast, data for the photocatalytic reactions support light-induced dissociation of a carbonyl ligand followed by a coordination-insertion sequence where the product is released by combination of a cobalt alkyl intermediate with the starting hydride, (R,R)-(iPrDuPhos)Co(CO)2H. These results demonstrate the versatility of catalysis with Earth-abundant metals as pathways involving open- versus closed-shell intermediates can be switched by the energy source.

Light-driven hydrogen production with CdSe quantum dots and a cobalt glutathione catalyst.

A photocatalytic hydrogen (H2) production system is reported using glutathione (GSH)-capped CdSe QDs with a cobalt precatalyst, yielding 130 000 mol H2 per mol cobalt over 48 hours. Analysis of the reaction mixtures after catalysis indicates that the active catalyst is a labile complex of cobalt and GSH formed in situ.