Bimetallic Cooperativity in Proton Reduction with an Amido‐Bridged Cobalt Catalyst
نویسندگان
چکیده
منابع مشابه
A robust and efficient cobalt molecular catalyst for CO2 reduction.
Visible-light driven CO2 reduction is considered to be a sustainable energy source. However, earth-abundant molecular catalysts with high efficiency and robustness towards solar-driven CO2 reduction are limited. Herein, we report a cobalt complex supported by a tetradentate tripodal ligand, which demonstrates catalytic solar-driven CO2 reduction with TON(CO) > 900 over 70 h in the presence of a...
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Linear trimetallic Co(III)/Co(II)/Co(III) cobalt complexes with bridging acyl-alkoxy ligands are electrocatalysts for the reduction of tosic acid in acetonitrile. The -OCMe2CH2COMe complex appears to operate homogeneously, and at a modest onset overpotential of 175 mV. A turnover frequency of ca. 80 s(-1) was observed at an overpotential of 300 mV.
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We report here the efficient reduction of CO2 to CO by cobalt aminopyridine macrocycles. The effect of the pendant amines on catalysis was investigated. Several cobalt complexes based on the azacalix[4](2,6)pyridine framework with different substitutions on the pendant amine groups have been synthesized (R = H (1), Me (2), and allyl (3)), and their electrocatalytic properties were explored. Und...
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چکیده ندارد.
15 صفحه اولLigand transformations and efficient proton/water reduction with cobalt catalysts based on pentadentate pyridine-rich environments.
A series of cobalt complexes with pentadentate pyridine-rich ligands is studied. An initial Co(II) amine complex 1 is prone to aerial oxidation yielding a Co(III) imine complex 2 that is further converted into an amide complex 4 in presence of adventitious water. Introduction of an N-methyl protecting group to the ligand inhibits this oxidation and gives rise to the Co(II) species 5. Both the C...
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ژورنال
عنوان ژورنال: Chemistry – A European Journal
سال: 2017
ISSN: 0947-6539,1521-3765
DOI: 10.1002/chem.201701982