Femtosecond charge transfer dynamics in artificial donor/acceptor systems: Switching from adiabatic to nonadiabatic regimes by small structural changes

被引:34
作者
Fiebig, T
Stock, K
Lochbrunner, S
Riedle, E
机构
[1] Tech Univ Munich, Inst Phys & Theoret Chem, D-85748 Garching, Germany
[2] LMU, Sekt Phys, LS Biomol Opt, D-80538 Munich, Germany
关键词
D O I
10.1016/S0009-2614(01)00869-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dynamics of intramolecular charge transfer (CT) in a family of conjugated aromatic electron donor/acceptor (D/ A) systems has been studied by femtosecond pump-probe spectroscopy. Although the compounds have very similar structures we observed vastly different CT dynamics, ranging from a few 100 fs to the nanosecond time range. These results show that specific modifications in the substitution scheme can lead to alterations of the relevant D/A orbitals and thus to drastic changes in the excited state electronic coupling. As a result the CT process switches from the ultrafast adiabatic to the slow nonadiabatic regime. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:81 / 88
页数:8
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