Aggregation kinetics of extended porphyrin and cyanine dye assemblies

被引:165
作者
Pasternack, RF [1 ]
Fleming, C
Herring, S
Collings, PJ
dePaula, J
DeCastro, G
Gibbs, EJ
机构
[1] Swarthmore Coll, Dept Chem, Swarthmore, PA 19081 USA
[2] Swarthmore Coll, Dept Phys & Astron, Swarthmore, PA 19081 USA
[3] Haverford Coll, Dept Chem, Haverford, PA 19041 USA
[4] Goucher Coll, Dept Chem, Towson, MD 21204 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(00)76316-8
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The kinetics of J-aggregate formation has been Studied for two chromophores, tetrakis-4-sulfonatophenylporphine in an acid medium and pseudoisocyanine on a polyvinylsulfonate template. The assembly processes differ both in their sensitivity to initiation protocols and in the reaction profiles they produce. The porphyrin's assembly kinetics, for example, displays an induction period unlike that of the cyanine dye. Two kinetic models are presented. For the porphyrin, an autocatalytic pathway in which the formation of an aggregation nucleus is rate-determining appears to be applicable; for the pseudoisocyanine dye, an equation derived for diffusion-limited aggregation of a fractal object satisfactorily fits the data. These models are shown to be useful for the analysis of kinetic data obtained for several biologically important aggregation processes.
引用
收藏
页码:550 / 560
页数:11
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