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Diiridium Bimetallic Complexes Function as a Redox Switch To Directly Split Carbonate into Carbon Monoxide and Oxygen
被引:28
作者:
Chen, Tsun-Ren
[1
]
Wu, Fang-Siou
[1
]
Lee, Hsiu-Pen
[1
]
Chen, Kelvin H. -C.
[1
]
机构:
[1] Natl Pingtung Univ, Dept Appl Chem, Pingtung 90003, Taiwan
关键词:
ELECTROCATALYTIC CO2 REDUCTION;
18 ELECTRON RULE;
PINCER COMPLEXES;
DIOXIDE;
CONVERSION;
FORMATE;
LIGAND;
SELECTIVITY;
MODEL;
WATER;
D O I:
10.1021/jacs.6b00715
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A pair of diiridium bimetallic complexes exhibit a special type of oxidation reduction reaction that could directly split carbonate into carbon monoxide and molecular oxygen-via a low-energy pathway needing no sacrificial reagent. One of the bimetallic complexes, Ir-III(mu-Cl)(2)Ir-III, can catch carbonato group from carbonate and reduce it to CO. The second complex, the rare bimetallic complex Ir-IV(mu-oxo)(2)Ir-IV, can react with chlorine to release O-2 by the oxidation of oxygen ions with synergistic oxidative effect of iridium ions and chlorine atoms. The activation energy needed for the key reaction is quite low (similar to 20 kJ/mol), which is far less than the dissociation energy of the C=O bond in CO2 (similar to 750 kJ/mol). These diiridium bimetallic complexes could be applied as a redox switch to split carbonate or combined with well-known processes in the chemical industry to build up a catalytic system to directly split CO2 into CO and O-2.
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页码:3643 / 3646
页数:4
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