Fukuzumi Shunichi, Inada Osamu, Suenobu Tomoyoshi
Department of Material and Life Science, Graduate School of Engineering, CREST, JST, Osaka University, Suita, Osaka 565-0871, Japan.
J Am Chem Soc. 2002 Dec 11;124(49):14538-9. doi: 10.1021/ja0272538.
The radical cation of an NADH analogue (BNAH: 1-benzyl-1,4-dihydronicotinamide) has been successfully detected as the transient absorption and ESR spectra in the thermal electron transfer from BNAH to Fe(bpy)33+ (bpy = 2,2'-bipyridine). The ESR spectra of the radical cations of BNAH and the dideuterated compound (BNAH-4,4'-d2) indicate that the observed radical cation is the keto form rather than the enol form in the tautomerization. The deprotonation rate and the kinetic isotope effects of the keto form of BNAH*+ were determined from the kinetic analysis of the electron-transfer reactions.
在从1-苄基-1,4-二氢烟酰胺(BNAH)到三(2,2'-联吡啶)铁(III)(bpy = 2,2'-联吡啶)的热电子转移过程中,已通过瞬态吸收和电子顺磁共振(ESR)光谱成功检测到NADH类似物(BNAH)的自由基阳离子。BNAH及其双氘代化合物(BNAH-4,4'-d2)的自由基阳离子的ESR光谱表明,所观察到的自由基阳离子在互变异构中是酮式而非烯醇式。通过对电子转移反应的动力学分析,确定了BNAH*+酮式的去质子化速率和动力学同位素效应。