Liu Shuo, Jung Jieun, Ohkubo Kei, Hicks Scott D, Bougher Curt J, Abu-Omar Mahdi M, Fukuzumi Shunichi
Brown Laboratory and Department of Chemistry, Purdue University , 560 Oval Drive, West Lafayette, Indiana 47907, United States.
Department of Chemistry and Nano Science, Ewha Womans University , Seoul 120-750, Korea.
Inorg Chem. 2015 Sep 21;54(18):9223-8. doi: 10.1021/acs.inorgchem.5b01777. Epub 2015 Sep 1.
Rate constants of electron self-exchange of high-valent oxo and imido complexes of chromium(V/IV) corrole have been determined in acetonitrile and toluene at various temperatures by electron paramagnetic resonance (EPR) line width variation of the EPR spectra. The observed activation enthalpies (ΔHobs(⧧)) of electron self-exchange of chromium(V)-oxo and -imido corrole with the corresponding chromium(IV) complexes are zero in toluene, whereas the ΔHobs(⧧) values are slightly positive in acetonitrile. Such activationless electron self-exchange transfer resulted in extremely fast electron-transfer reactions of chromium(V)-oxo and -imido corrole in sharp contrast with slow electron-transfer reactions of other high-valent metal-oxo and -imido complexes.