Yuasa Junpei, Fukuzumi Shunichi
Department of Material and Life Science, Graduate School of Engineering, Osaka University, SORST, Japan Science and Technology Agency (JST), Suita, Osaka 565-0871, Japan.
J Am Chem Soc. 2006 Nov 8;128(44):14281-92. doi: 10.1021/ja0604562.
Efficient energy transfer from Ru(bpy)(3)(2+) (bpy = 2,2'-bipyridine, denotes the excited state) to 3,6-disubstituted tetrazines [R(2)Tz: R = Ph (Ph(2)Tz), 2-chlorophenyl [(ClPh)(2)Tz], 2-pyridyl (Py(2)Tz)] occurs to yield the triplet excited states of tetrazines ((3)R(2)Tz()), which have longer lifetimes and higher oxidizing ability as compared with those of Ru(bpy)(3)(2+). The dynamics of hydrogen-transfer reactions from NADH (dihydronicotinamide adenine dinucleotide) analogues has been examined in detail using (3)R(2)Tz() by laser flash photolysis measurements. Whether formal hydrogen transfer from NADH analogues to (3)R(2)Tz() proceeds via a one-step process or sequential electron and proton transfer processes is changed by a subtle difference in the electron donor ability and the deprotonation reactivity of the radical cations of NADH analogues as well as the electron-acceptor ability of (3)R(2)Tz() and the protonation reactivity of R(2)Tz()(-). In the case of (3)Ph(2)Tz(), which is a weaker electron acceptor than the other tetrazine derivatives [(ClPh)(2)Tz; Py(2)Tz], direct one-step hydrogen transfer occurs from 10-methyl-9,10-dihydroacridine (AcrH(2)) to (3)Ph(2)Tz() without formation of the radical cation (AcrH(2)()(+)). The rate constant of the direct hydrogen transfer from AcrH(2) to (3)Ph(2)Tz() is larger than that expected from the Gibbs energy relation for the rate constants of electron transfer from various electron donors to (3)Ph(2)Tz(), exhibiting the primary deuterium kinetic isotope effect. On the other hand, hydrogen transfer from 9-isopropyl-10-methyl-9,10-dihydroacridine (AcrHPr(i)) and 1-benzyl-1,4-dihydronicotinamide (BNAH) to (3)R(2)Tz(*) occurs via sequential electron and proton transfer processes, when both the radical cations and deprotonated radicals of NADH analogues are detected by the laser flash photolysis measurements.
能量从Ru(bpy)(3)(2+)(bpy = 2,2'-联吡啶,表示激发态)高效转移至3,6-二取代四嗪[R(2)Tz:R = 苯基(Ph(2)Tz)、2-氯苯基[(ClPh)(2)Tz]、2-吡啶基(Py(2)Tz)],生成四嗪的三重激发态((3)R(2)Tz()),与Ru(bpy)(3)(2+)相比,其具有更长的寿命和更高的氧化能力。通过激光闪光光解测量,使用(3)R(2)Tz()详细研究了来自NADH(二氢烟酰胺腺嘌呤二核苷酸)类似物的氢转移反应动力学。NADH类似物的自由基阳离子的电子供体能力和去质子化反应性以及(3)R(2)Tz()的电子受体能力和R(2)Tz()(-)的质子化反应性的细微差异,改变了从NADH类似物到(3)R(2)Tz()的形式氢转移是通过一步过程还是顺序电子和质子转移过程进行。在(3)Ph(2)Tz()的情况下,它是比其他四嗪衍生物[(ClPh)(2)Tz;Py(2)Tz]更弱的电子受体,直接一步氢转移从10-甲基-9,10-二氢吖啶(AcrH(2))发生至(3)Ph(2)Tz(),而不形成自由基阳离子(AcrH(2)()(+))。从AcrH(2)到(3)Ph(2)Tz()的直接氢转移速率常数大于根据从各种电子供体到(3)Ph(2)Tz()的电子转移速率常数的吉布斯能量关系预期的值,表现出初级氘动力学同位素效应。另一方面,当通过激光闪光光解测量检测到NADH类似物的自由基阳离子和去质子化自由基时,从9-异丙基-10-甲基-9,10-二氢吖啶(AcrHPr(i))和1-苄基-1,4-二氢烟酰胺(BNAH)到(3)R(2)Tz(*)的氢转移通过顺序电子和质子转移过程发生。