ELECTRON-SPIN DYNAMICS OF PHOTOEXCITED CORANNULENE-LITHIUM COMPLEXES IN TETRAHYDROFURAN - FOURIER-TRANSFORM ELECTRON-PARAMAGNETIC-RESONANCE

被引:19
|
作者
ZILBER, G
ROZENSHTEIN, V
CHENG, PC
SCOTT, LT
RABINOVITZ, M
LEVANON, H
机构
[1] HEBREW UNIV JERUSALEM,DEPT ORGAN CHEM,IL-91904 JERUSALEM,ISRAEL
[2] HEBREW UNIV JERUSALEM,DEPT PHYS CHEM,IL-91904 JERUSALEM,ISRAEL
[3] HEBREW UNIV JERUSALEM,FARKAS CTR LIGHT INDUCED PROC,IL-91904 JERUSALEM,ISRAEL
[4] BOSTON COLL,DEPT CHEM,MERKERT CHEM CTR,CHESTNUT HILL,MA 02167
关键词
D O I
10.1021/ja00148a014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tetrahydrofuran (THF) solutions of corannulene (Cor) reduced by lithium metal exhibit electron paramagnetic resonance (EPR) features that depend on the reduction stage of Cor, the temperature, and the nuclear spin (isotope effect). Photoexcitation of these solutions results in EPR emissive spectra, attributed to the trianion, Cor(3.-), and to the photoelectron, e(photo)(-). These electron spin polarized (ESP) effects are discussed within the framework of intramolecular electron transfer reactions of ion complexes of highly charged constituents, in conjunction with ESP mechanisms that take into account radical-triplet interactions.
引用
收藏
页码:10720 / 10725
页数:6
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