Abstract
Reactions of [Co(dmgH)(dmgH2)Cl2] (dmgH = dimethylglyoxime) or [Co(chdH)(chdH2)Cl2] (chd = 1,2-cyclohexanedione dioximate) with 4,4′-bipyridine in MeOH in the presence of Et3N resulted in the formation of binuclear cobaloxime complexes [{Co(dmgH)2Cl}2(bipy)] (1, bipy = 4,4′-bipyridine) and [{Co(chdH)2Cl}2(bipy)] (2) in good yields. Complexes 1 and 2 were characterized by NMR and X-ray crystallography. Both 1 and 2 were found to be molecular catalysts for light-driven hydrogen evolution in the presence of Eosin Y as photosensitizer and triethanolamine as sacrificial electron donor in aqueous acetonitrile solutions upon irradiation.
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We are grateful to the National Natural Science Foundation of China (Grant No. 21202115), The Research Fund for the Doctoral Program of Higher Education (Grant No. 20100032120070) and Tianjin Research Program of Application Foundation and Advanced Technology (Grant No. 13JCQNJC06100). The author gratefully acknowledges the support of K.C. Wong Education Foundation.
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Liu, XF., Zhang, YX. & Yan, J. 4,4′-Bipyridine axially coordinated binuclear cobaloxime complexes as molecular catalysts for light-driven hydrogen evolution. Transition Met Chem 40, 305–311 (2015). https://doi.org/10.1007/s11243-015-9918-1
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DOI: https://doi.org/10.1007/s11243-015-9918-1