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机构地区:[1]Department of Chemistry and Chemical Engineering, Hunan University, Changsha 410082 PRC [2]Department of Chemistry, Jilin University, Changchun 130023 PRC
出 处:《Chinese Science Bulletin》1993年第12期998-1001,共4页
基 金:Project supported by the National Natural Science Foundation of China
摘 要:It is now widely recognized that coenzyme B<sub>12</sub>-dependent rearrangements are caused by homolytic dissociation of the Co-C bond giving rise to a 5’-deoxyadenosyl radical. The Co-C bonding strength is related to the electronic and steric effect of the 5’-deoxyadenosyl radical and the axial organic base, playing a key role in the catalytic cycle. To clarify the mechanism of Co-C bond breaking in coenzyme B<sub>12</sub>, many experimental and theoretic researches on B<sub>12</sub> model compounds have been conducted, especially on the
关 键 词:COENZYME B12 model compounds ELECTROCHEMISTRY quantum chemistry.
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