Unusual dynamic relaxation of triplet-excited meso-phenyl-substituted porphyrins and their chemical dimers at room temperatures

被引:55
作者
Knyukshto, V [1 ]
Zenkevich, E [1 ]
Sagun, E [1 ]
Shulga, A [1 ]
Bachilo, S [1 ]
机构
[1] Byelarussian Acad Sci, Inst Mol & Atom Phys, Minsk 220072, BELARUS
关键词
D O I
10.1016/S0009-2614(98)01096-3
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
It has been found that for mono- and di-meso-phenyl-substituted octaethylporphyrin (OEPs), etioporphyrins, corresponding Zn complexes and OEP chemical dimers (with a meso-phenyl spacer) a drastic shortening of triplet lifetimes from a ms to mu s timescale in deaerated toluene solutions at 295 K takes place without any changes of the spectral-kinetic parameters of the S-0 and S-1 states. The observed effects are connected with torsion librations of the phenyl ring around a single C-C bond in sterically encumbered porphyrins leading to non-planar dynamic distorted conformations in excited T-1 states accompanied by an enhancement of the T-1-state nonradiative deactivation pathways. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 108
页数:12
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