期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 131, 期 47, 页码 17127-17134出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja9045235
关键词
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资金
- Ministry of Education, Culture, Sports, Science and Technology, Japan
- Korea Science and Engineering Foundation
- KOSEF/MEST [R31-2008-000-10010-0]
- [19205019]
- [19750034]
- [21750146]
Hydride transfer from dihydronicotinamide adenine dinuclectide (NADH) analogs to a manganese(IV)-oxo porphyrin complex, (TMP)Mn(IV)(O) [TMP = 5,10,15,20-tetrakis(2,4,6-trimethylphenyl)porphyrin], occurs via disproportionation of (TMP)Mn(IV)(O) to [(TMP)Mn(III)](+) and [(TMP)Mn(V)(O)](+) that acts as the actual hydride acceptor. In contrast, electron transfer from ferrocene derivatives to (TMP)Mn(IV)(O) occurs directly to afford ferricenium ions and (TMP)Mn(III)(OH) products. The disproportionation rate constant of (TMP)Mn(IV)(O) was determined by the dependence of the observed second-order rate constants on concentrations of NADH analogs to be (8.0 +/- 0.6) x 10(6) M(-1) s(-1) in acetonitrile at 298 K. The disproportionation rate constant of (TMP)Mn(IV)(O) in hydride-transfer reactions increases linearly with increasing acid concentration, whereas the rate constant of electron transfer from ferrocene to (TMP)Mn(IV)(O) remains constant irrespective of the acid concentration. The rate constants of electron transfer from a series of ferrocene derivatives to (TMP)Mn(IV)(O) were evaluated in light of the Marcus theory of electron transfer to determine the reorganization energy of electron transfer by the (TMP)Mn(IV)(O) complex.
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