Asymmetric double proton transfer of excited 1:1 7-azaindole/alcohol complexes with anomalously large and temperature-independent kinetic isotope effects

被引:82
作者
Kwon, OH
Lee, YS
Park, HJ
Kim, Y
Jang, DJ
机构
[1] Seoul Natl Univ, Sch Chem, Seoul 151742, South Korea
[2] Kyung Hee Univ, Dept Chem, Kyunggido 449701, Yongin, South Korea
关键词
hydrogen bonds; kinetic isotope effects; N-heterocycles; proton transfer; time-resolved spectroscopy;
D O I
10.1002/anie.200461102
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bridging alcohols, tunneling protons: The intrinsic proton-transfer dynamics of cyclic H-bonded 1:1 7-azaindole/alcohol complexes in n-alkanes has been investigated at the lowest-lying excited singlet state with variation of alcohol, solvent, isotope, and temperature by using static and time-resolved spectroscopy. The proton transfer occurs asymmetrically, and the rate is governed by tunneling although it is assisted by heavy-atom motions.
引用
收藏
页码:5792 / 5796
页数:5
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