Excited state behaviour of pentahelicene dinitriles

被引:20
作者
Görner, H
Stammel, C
Mattay, J
机构
[1] Max Planck Inst Strahlenchem, D-45413 Mulheim, Germany
[2] Univ Kiel, Inst Organ Chem, D-24098 Kiel, Germany
关键词
photophysics; fluorescence quenching; photoinduced electron transfer; triplet state; singlet oxygen; quantum yields;
D O I
10.1016/S1010-6030(98)00423-7
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 excited singlet and triplet states 2, 13-dicyano[5]helicene (1) and two para-dicyno[5]helicenes containing one and two methyl groups (2 and 3, respectively) were studied in solvents of different polarity as a function of temperature. Fluorescence quenching by electron donors such as triethyl amine indicated photoinduced electron transfer. In the absence of additives triplet states were observed by flash photolysis. The triplet lifetime at room temperature was rather short (<1 mu s) and the decay limited by intramolecular processes, e.g. charge transfer in the cases of 2 or 3. Luminescence of singlet molecular oxygen, O-2((1)Delta(g)), was observed with moderate and low quantum yield for 1 and 3, respectively. For 1-3, the triplet lifetime increases by six orders of magnitude on going to -196 degrees C. Two subsequently formed triplet states were observed for 3 at lower temperatures. The effects of temperature and solvent polarity on the quantum yields of fluorescence and phosphorescence and the spectroscopic and kinetic triplet absorption properties were examined. The influence of substituents on the deactivation pathways of excited pentahelicenes are discussed. (C) 1999 Elsevier Science S.A. All rights reserved.
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页码:171 / 179
页数:9
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