三态1-硝基萘与反式二苯乙烯的竞争性能量和电子转移反应

Laser Chemistry Pub Date : 1900-01-01 DOI:10.1155/1999/92415
T. Fournier, G. Scholes, I. Gould, S. Tavender, D. Phillips, A. Parker
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引用次数: 0

摘要

利用时间分辨共振拉曼(TR3)研究了1-硝基萘(1NN)在不同溶剂中的第一三重态激发态,并结合从头计算确定了该态在不同极性环境下的性质和几何形状。本文报道了三态1NN与反式二苯乙烯(tS)在非极性和极性溶剂中反应的瞬态吸收和TR3研究。在极性溶液中,31NN充当电子受体,而在非极性溶液中只观察到向tS的能量转移。此外,在高浓度的tS下,自由基阳离子tS
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Triplet 1-nitronaphthalene and competitive energy and electron transfer reactions with trans-stilbene
A time resolved resonance Raman (TR3) study of 1-nitronaphthalene (1NN) first triplet excited state in various solvents is combined with ab initio calculations to determine the nature and the geometry of this state in environments of different polarity. A transient absorption and TR3 study of the reactions of triplet 1NN with trans-stilbene (tS) in solution in both non-polar and polar solvents is reported. In polar solution, 31NN acts as an electron acceptor whereas in non-polar solution only energy transfer to tS is observed. Moreover, at high concentrations of tS, the radical cation tS
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