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Indexed by:期刊论文

Date of Publication:2010-09-23

Journal:JOURNAL OF PHYSICAL CHEMISTRY C

Included Journals:SCIE、EI、Scopus

Volume:114

Issue:37

Page Number:15868-15874

ISSN No.:1932-7447

Abstract:Hydrogen evolution was observed from the noble-metal-free catalyst systems, comprising Rose Bengal, BFx-bridged cobaloximes, and triethylamine, in an aqueous solution under irradiation of visible light. Two types of BFx-bridged cobaloximes namely, the annulated cobaloximes [Co(dmgBF(2))(2)(H2O)(2)] (1, dmgBF(2) = (difluoroboryl)dimethylglyoximate anion) and [Co(dpgBF(2))(2)(H2O)(2)] (2, dpgBF(2) =(difluoroboryl)diphenylglyoximate anion), and the clathrochelated cobaloximes [Co(dmg(BF)(2/3))(3)](BF4) (3) and [Co(dpg(BF)(2/3))(3)](BF4) (4)-were used as catalysts. Among the four cobalt complexes, complex 1 displayed the highest hydrogen-evolving efficiency, with turnovers up to 327. Complexes 2 and 4 that bear the diphenylglyoximate ligands exhibited much lower efficiencies as compared with their analogues 1 and 3 that have the dimethylglyoximate ligands. The hydrogen-evolving efficiency of the annulated cobalt(II) complex 1 that contains two labile axial ligands is more than three times as high as that of the encapsulated cobalt(III) complex 3 that has a single macrobicyclic ligand. The different pathways for formation of the cobalt(I) species from these two types of cobaloximes are discussed on the basis of the results obtained from fluorescence and laser flash photolysis spectroscopic studies.