Photokinetics in tetraphenylporphyrin - molecular oxygen system at gas/solid interfaces: effect of singlet oxygen quenchers on oxygen-induced delayed fluorescence

被引:20
|
作者
Levin, PP
Costa, SMB
机构
[1] Univ Tecn Lisboa, Ctr Quim Estrutural, Inst Super Tecn, P-1049001 Lisbon, Portugal
[2] Russian Acad Sci, Inst Biochem Phys, Moscow 117334, Russia
基金
俄罗斯基础研究基金会;
关键词
D O I
10.1016/S0301-0104(00)00365-7
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 oxygen quenching of excited states and concomitant delayed fluorescence (DF) of meso-tetraphenylporphyrin (TPP) adsorbed on alumina (Al2O3) were studied at different TPP and O-2 concentrations and temperatures by the diffuse-reflectance laser flash technique. The formation of O-1(2) in the course of (TPP)-T-3 quenching by O-3(2) is followed by the energy transfer from O-1(2) to (TPP)-T-3 (O-1(2) feedback) with the generation of TPP fluorescent state. The global kinetic analysis of DF revealed variations on kinetic parameters with surface loading which match the aggregation of TPP on the surface. In concentrated samples the energy exchange between O-1(2) and O-3(2) accelerates the O-1(2) feedback more than 10 times. The key role of O-1(2) in oxygen-induced DF is confirmed by the DF quenching by coadsorbed O-1(2) quenchers (NaN3, 3-methylindole, 1.4-diazabicyclo[2.2.2]octane). This process is in part controlled by the surface which enhances the efficiencies of amine quenchers but reduces that of NaN3 when compared with the corresponding efficiencies in solution. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:423 / 436
页数:14
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