ULTRAFAST PHOTOINDUCED ELECTRON-TRANSFER REACTIONS IN SUPRAMOLECULAR ARRAYS - FROM CHARGE SEPARATION AND STORAGE TO MOLECULAR SWITCHES

被引:25
作者
WASIELEWSKI, MR
ONEIL, MP
GOSZTOLA, D
NIEMCZYK, MP
SVEC, WA
机构
[1] Chemistry Division, Argonne National Laboratory, Argonne, Illinois
关键词
D O I
10.1351/pac199264091319
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photochemical electron transfer reactions on a picosecond time scale have been studied in two covalently-linked donor-acceptor systems. The first molecule is a chlorophyll-porphyrin-quinone triad that closely mimics photosynthetic charge separation by undergoing picosecond electron transfer in low temperature glasses to yield a radical ion pair that lives for 2 ms and exhibits spin-polarization. The second molecule is an electron donor-acceptor-donor molecule, consisting of two porphyrin donors rigidly attached to opposite ends of the two-electron acceptor N,N'-diphenyl-3,4,9,10-perylenebis(dicarboximide). This molecule acts as a light intensity dependent molecular switch on a picosecond time scale.
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收藏
页码:1319 / 1325
页数:7
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