Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 79 checked references that resolve
resolves10.1126/science.aav3506What would it take for renewably powered electrosynthesis to displace petrochemical processes?
resolves10.1021/cr400461pStructure, Function, and Mechanism of the Nickel Metalloenzymes, CO Dehydrogenase, and Acetyl-CoA Synthase
resolves10.1021/acs.accounts.9b00619Hybrid Catalysts for Artificial Photosynthesis: Merging Approaches from Molecular, Materials, and Biological Catalysis
resolves10.1021/ja00544a035Electrocatalytic reduction of carbon dioxide by using macrocycles of nickel and cobalt
resolves10.1039/c39840001315Nickel(II)-cyclam: an extremely selective electrocatalyst for reduction of CO2 in water
resolves10.1039/c2ee22528jNickel(ii) macrocycles: highly efficient electrocatalysts for the selective reduction of CO2 to CO
resolves10.1021/ic3001619Homogeneous CO<sub>2</sub> Reduction by Ni(cyclam) at a Glassy Carbon Electrode
resolves10.1039/c39740000158Electrocatalysis by metal phthalocyanines in the reduction of carbon dioxide
resolves10.1126/science.1224581A Local Proton Source Enhances CO
<sub>2</sub>
Electroreduction to CO by a Molecular Fe Catalyst
resolves10.1021/jacs.6b07014Through-Space Charge Interaction Substituent Effects in Molecular Catalysis Leading to the Design of the Most Efficient Catalyst of CO
<sub>2</sub>
-to-CO Electrochemical Conversion
resolves10.1126/science.aax4608Molecular electrocatalysts can mediate fast, selective CO
<sub>2</sub>
reduction in a flow cell
resolves10.1039/C39840000328Electrocatalytic reduction of carbon dioxide mediated by Re(bipy)(CO)<sub>3</sub>Cl (bipy = 2,2′-bipyridine)
resolves10.1021/ic1008363Re(bipy-tBu)(CO)<sub>3</sub>Cl−improved Catalytic Activity for Reduction of Carbon Dioxide: IR-Spectroelectrochemical and Mechanistic Studies
resolves10.1039/C8CS00546JThe value of enzymes in solar fuels research – efficient electrocatalysts through evolution
resolves10.1021/acscatal.9b04746Mechanistic Understanding of CO
<sub>2</sub>
Reduction Reaction (CO2RR) Toward Multicarbon Products by Heterogeneous Copper-Based Catalysts
resolves10.1038/nature08969A molecular molybdenum-oxo catalyst for generating hydrogen from water
resolves10.1021/ja202743rMolecular Cobalt Pentapyridine Catalysts for Generating Hydrogen from Water
resolves10.1039/c1cc15071eElectrocatalytic reduction of CO2 to CO by polypyridyl ruthenium complexes
resolves10.1021/jacs.9b01735The <i>Trans</i> Effect in Electrocatalytic CO<sub>2</sub> Reduction: Mechanistic Studies of Asymmetric Ruthenium Pyridyl-Carbene Catalysts
resolves10.1021/jacs.0c02912Kinetics of the <i>Trans</i> Effect in Ruthenium Complexes Provide Insight into the Factors That Control Activity and Stability in CO<sub>2</sub> Electroreduction
resolves10.1002/cssc.201900730Electrocatalytic CO<sub>2</sub> Reduction with a Ruthenium Catalyst in Solution and on Nanocrystalline TiO<sub>2</sub>
resolves10.1073/pnas.1907740116Steering CO
<sub>2</sub>
electroreduction toward ethanol production by a surface-bound Ru polypyridyl carbene catalyst on N-doped porous carbon
resolves10.1002/anie.201209911The Electronic States of Rhenium Bipyridyl Electrocatalysts for CO<sub>2</sub> Reduction as Revealed by X‐ray Absorption Spectroscopy and Computational Quantum Chemistry
resolves10.1021/acscatal.7b03971Kinetic and Mechanistic Effects of Bipyridine (bpy) Substituent, Labile Ligand, and Brønsted Acid on Electrocatalytic CO<sub>2</sub> Reduction by Re(bpy) Complexes
resolves10.1021/ja406456gElucidation of the Selectivity of Proton-Dependent Electrocatalytic CO<sub>2</sub> Reduction by <i>fac</i>-Re(bpy)(CO)<sub>3</sub>Cl
resolves10.1039/C8CC00266EElectrocatalytic CO
<sub>2</sub>
reduction with nickel complexes supported by tunable bipyridyl-N-heterocyclic carbene donors: understanding redox-active macrocycles
resolves10.1021/acscatal.9b00708Robust and Selective Cobalt Catalysts Bearing Redox-Active Bipyridyl-<i>N</i>-heterocyclic Carbene Frameworks for Electrochemical CO<sub>2</sub> Reduction in Aqueous Solutions
resolves10.1126/science.aac8343Covalent organic frameworks comprising cobalt porphyrins for catalytic CO
<sub>2</sub>
reduction in water
resolves10.1021/jacs.7b11940Reticular Electronic Tuning of Porphyrin Active Sites in Covalent Organic Frameworks for Electrocatalytic Carbon Dioxide Reduction
resolves10.26434/chemrxiv.11911383.v1An Iron Pyridyl-Carbene Catalyst for Low Overpotential CO2 reduction to CO: Mechanistic Comparisons with the Ruthenium Analogue and Photochemical Promotion
resolves10.1021/ja207842rA Cobalt–Dithiolene Complex for the Photocatalytic and Electrocatalytic Reduction of Protons
resolves10.1073/pnas.1120757109Cobalt-dithiolene complexes for the photocatalytic and electrocatalytic reduction of protons in aqueous solutions
resolves10.1021/ja5019755Mechanism of the Electrocatalytic Reduction of Protons with Diaryldithiolene Cobalt Complexes
resolves10.1021/acscentsci.7b00160Electroreduction of CO<sub>2</sub> Catalyzed by a Heterogenized Zn–Porphyrin Complex with a Redox-Innocent Metal Center
resolves10.1039/C5SC01414JBioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
resolves10.1039/C7SC04682KPositional effects of second-sphere amide pendants on electrochemical CO
<sub>2</sub>
reduction catalyzed by iron porphyrins
resolves10.1021/acs.inorgchem.0c01162An NADH-Inspired Redox Mediator Strategy to Promote
Second-Sphere Electron and Proton Transfer for Cooperative Electrochemical
CO2 Reduction Catalyzed by Iron Porphyrin
resolves10.1021/acs.inorgchem.5b00658Water-Soluble Iron(IV)-Oxo Complexes Supported by Pentapyridine Ligands: Axial Ligand Effects on Hydrogen Atom and Oxygen Atom Transfer Reactivity
resolves10.1021/ic801535vCalibration of Modern Density Functional Theory Methods for the Prediction of <sup>57</sup>Fe Mössbauer Isomer Shifts: Meta-GGA and Double-Hybrid Functionals
resolves10.1021/acsomega.7b00595Density Functional Calculations for Prediction of <sup>57</sup>Fe Mössbauer Isomer Shifts and Quadrupole Splittings in β-Diketiminate Complexes
resolves10.1021/acs.inorgchem.5b02136Standard Reduction Potentials for Oxygen and Carbon
Dioxide Couples in Acetonitrile and
<i>N</i>
,
<i>N</i>
-Dimethylformamide
resolves10.1021/acscatal.5b00656Thermodynamic Aspects of Electrocatalytic CO
<sub>2</sub>
Reduction in Acetonitrile and with an Ionic Liquid as Solvent or Electrolyte
resolves10.1021/acsenergylett.7b00548Standard Electrode Potentials for the Reduction of CO<sub>2</sub> to CO in Acetonitrile–Water Mixtures Determined Using a Generalized Method for Proton-Coupled Electron-Transfer Reactions
resolves10.1016/S0020-1693(99)00407-7Conversion constants for redox potentials measured versus different reference electrodes in acetonitrile solutions at 25°C
resolves10.1021/acscatal.9b04687Highly Efficient Electrocatalytic Reduction of CO<sub>2</sub> to CO by a Molecular Chromium Complex
resolves10.1021/jacs.6b08776Turning on the Protonation-First Pathway for Electrocatalytic CO<sub>2</sub>Reduction by Manganese Bipyridyl Tricarbonyl Complexes
resolves10.1021/acs.inorgchem.8b00450Activation of Co(I) State in a Cobalt-Dithiolato Catalyst for Selective and Efficient CO<sub>2</sub> Reduction to CO
resolves10.1039/C8CS00851EOn decomposition, degradation, and voltammetric deviation: the electrochemist's field guide to identifying precatalyst transformation
resolves10.1021/ic500658xEvaluation of Homogeneous Electrocatalysts by Cyclic Voltammetry
resolves10.1021/ja303560cTurnover Numbers, Turnover Frequencies, and Overpotential in Molecular Catalysis of Electrochemical Reactions. Cyclic Voltammetry and Preparative-Scale Electrolysis
resolves10.1021/ja3106187Correction to Turnover Numbers, Turnover Frequencies, and Overpotential in Molecular Catalysis of Electrochemical Reactions. Cyclic Voltammetry and Preparative-Scale Electrolysis
resolves10.1021/ja204489eElectrocatalytic Oxidation of Formate by [Ni(P
<sup>R</sup>
<sub>2</sub>
N
<sup>R′</sup>
<sub>2</sub>
)
<sub>2</sub>
(CH
<sub>3</sub>
CN)]
<sup>2+</sup>
Complexes
resolves10.1021/jacs.7b07709Electrocatalytic CO<sub>2</sub> Reduction by Imidazolium-Functionalized Molecular Catalysts
resolves10.1021/jacs.8b05658A Thiourea Tether in the Second Coordination Sphere as a Binding Site for CO<sub>2</sub> and a Proton Donor Promotes the Electrochemical Reduction of CO<sub>2</sub> to CO Catalyzed by a Rhenium Bipyridine-Type Complex
resolves10.1021/ic048765lX-ray Absorption Spectroscopic Investigation of the Spin-Transition Character in a Series of Single-Site Perturbed Iron(II) Complexes
resolves10.1021/ic2027219Experimental Fingerprints for Redox-Active Terpyridine in [Cr(tpy)<sub>2</sub>](PF<sub>6</sub>)<sub><i>n</i></sub> (<i>n</i> = 3–0), and the Remarkable Electronic Structure of [Cr(tpy)<sub>2</sub>]<sup>1–</sup>
resolves10.1002/ejic.201200232Electronic Structures of the Electron Transfer Series [M(bpy)
<sub>3</sub>
]
<i>
<sup>n</sup>
</i>
, [M(tpy)
<sub>2</sub>
]
<i>
<sup>n</sup>
</i>
, and [Fe(
<sup>t</sup>
bpy)
<sub>3</sub>
]
<i>
<sup>n</sup>
</i>
(M = Fe, Ru;
<i>n</i>
= 3+, 2+, 1+, 0, 1–): A Mössbauer Spectroscopic and DFT Study
resolves10.1021/ic7010343Spectroscopic and Computational Studies of a Ru(II) Terpyridine Complex: The Importance of Weak Intermolecular Forces to Photophysical Properties
resolves10.1039/c3sc51339dSelective electrocatalytic reduction of carbon dioxide to formate by a water-soluble iridium pincer catalyst
resolves10.1073/pnas.1507063112Efficient and selective molecular catalyst for the CO
<sub>2</sub>
-to-CO electrochemical conversion in water
resolves10.1021/acscatal.5b01708An Iron Electrocatalyst for Selective Reduction of CO<sub>2</sub> to Formate in Water: Including Thermochemical Insights
resolves10.1021/acscatal.7b03275Selective Electrocatalysis of a Water-Soluble Rhenium(I) Complex for CO
<sub>2</sub>
Reduction Using Water As an Electron Donor
resolves10.1126/science.aaw7515Atomically dispersed Fe
<sup>3+</sup>
sites catalyze efficient CO
<sub>2</sub>
electroreduction to CO
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