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Ultrafast UV-vibrational spectroscopy was used to investigate how vibrational excitation of the bridge changes photoinduced electron transfer between donor (dimethylaniline) and acceptor (anthracene) moieties bridged by a guanosine-cytidine base pair (GC). The charge-separated (CS) state yield is found to be lowered by high-frequency bridge mode excitation. The effect is linked to a dynamic modulation of the donor-acceptor coupling interaction by weakening of H-bonding and/or by disruption of the bridging base-pair planarity.
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Zhiwei Lin
Fujian Medical University
Candace M. Lawrence
Tulane University
Dequan Xiao
Dalian Institute of Chemical Physics
Journal of the American Chemical Society
Duke University
Tulane University
University of Cyprus
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Lin et al. (Tue,) studied this question.
synapsesocial.com/papers/6a05005ac678e6ad4619c1c6 — DOI: https://doi.org/10.1021/ja907041t
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