Resolution of concerted versus sequential mechanisms in photo-induced double-proton transfer reaction in 7-azaindole H-bonded dimer

被引:109
作者
Catalán, J
del Valle, JC
Kasha, M [1 ]
机构
[1] Univ Autonoma Madrid, Dept Quim Fis Aplicada, E-28049 Madrid, Spain
[2] Florida State Univ, Dept Chem, Tallahassee, FL 32306 USA
[3] Florida State Univ, Inst Mol Biophys, Tallahassee, FL 32306 USA
关键词
base pairs; photo-tautomerism;
D O I
10.1073/pnas.96.15.8338
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The experimental and theoretical bases for a synchronous or concerted double-proton transfer in centrosymmetric H-bonded electronically excited molecular dimers are presented. The prototype model is the 7-azaindole dimer, New research offers confirmation of a concerted mechanism for excited-state biprotonic transfer. Recent femtosecond photoionization and coulombic explosion techniques have given rise to time-of-flight MS observations suggesting sequential two-step biprotonic transfer for the same dimer. We interpret the overall species observed in the time-of-flight experiments as explicable without conflict with the concerted mechanism of proton transfer.
引用
收藏
页码:8338 / 8343
页数:6
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