PHOTOPHYSICAL BEHAVIOR OF ZINC TETRAPHENYLPORPHYRINS IN SOLUTIONS AND POLYMER-FILMS

被引:8
作者
CROUCH, AM
LANGFORD, CH
机构
[1] Laboratories for Inorganic Materials, Department of Chemistry, Concordia University, Montreal, Que. H3G 1M8
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/1010-6030(90)87090-X
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 fluorescence and phosphorescence of zinc tetraphenylporphyrin (ZnTPP) and its tatrasulfonated derivative (ZnTPPS) were evaluated using time-resolved luminescence and absorption measurements in three environments: dilute solution, solutions containing polyvinylpyridine (PVP) and quaternary-ammonium-ion-derivatized styrene copolymer and films of the polymers. Both the singlet and triplet lifetimes are reduced in highly doped films or in solution in the presence of small polymer concentrations where attachment of the porphyrin leads to low average porphyrin-porphyrin separations. In contrast, for poorly doped films or high polymer concentrations in solution, porphyrins bound to pyridine moieties in PVP or to the cation sites of the anionic copolymer exhibit increases in both the singlet and triplet lifetimes. There is no parallel effect for ZnTPP axially bound by dissolution in pyridine. Flash experiments reveal a new relaxation pathway for ZnTPP-pyridine. © 1990.
引用
收藏
页码:55 / 64
页数:10
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