A combined laser flash photolysis, density functional theory and atoms in molecules study of the photochemical hydrogen abstraction by pyrene-4,5-dione

被引:25
|
作者
de Lucas, Nanci C. [1 ]
Elias, Monica M. [1 ]
Firme, Caio L. [1 ]
Correa, Rodrigo J. [1 ]
Garden, Simon J. [1 ]
Netto-Ferreira, Jose Carlos [2 ]
Nicodem, David E. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Quim, BR-21941909 Rio De Janeiro, Brazil
[2] Univ Fed Bahia, Dept Quim Geral & Inorgan, BR-40170290 Bahia Blanca, Buenos Aires, Argentina
关键词
Laser flash photolysis; Ortho-quinone; Triplet excited state; DFT; Hydrogen atom transfer; ELECTRON-TRANSFER; BETA-LAPACHONE; PHOTOREDUCTION; SOLVENT; 9,10-PHENANTHRENEQUINONE; RADICALS; PHOTOREACTIVITY; N; PI(ASTERISK); PHENOLS; KETONES;
D O I
10.1016/j.jphotochem.2008.08.014
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 photochemical hydrogen abstraction reaction of pyrene-4,5-dione (3) has been investigated by laser flash photolysis. Excitation (lambda = 355 nm) of a degassed solution of 3 in acetonitrile resulted in the formation of a detectable transient with absorption maxima at 380 and 470 nm. This transient decays with a lifetime of around 4.8 mu s and is quenched by oxygen. This transient is most probably a triplet state of 3. Addition of hydrogen donors, such as 2-propanol; 1,4-cyclohexadiene or 4-methoxyphenol led to the formation of a new transient with.. at 380,500 mm and a broad absorption at 640 rim. This new transient slowly decays with second order kinetics and was assigned to the semiquinone radical obtained from the hydrogen abstraction reaction. Using DFT and AIM calculations the reactivity of 3 and 9,10-phenanthrenequinone (I) is best interpreted as a proton coupled electron transfer like mechanism for the hydrogen abstraction from 2-propanol. (C) 2008 Elsevier B.V. All rights reserved.
引用
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页码:1 / 7
页数:7
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