CONTRACTION KINETICS OF STRETCHED POLYMERS VIA LOCAL CONFORMATIONAL-CHANGES

被引:2
|
作者
POLAND, D
机构
[1] Department of Chemistry, Johns Hopkins University, Baltimore
关键词
D O I
10.1021/ma00053a036
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We use the beginning coefficients in exact time power series to study the kinetics of the conformation-to-random coil contraction of a model polymer system. We treat a two-dimensional (2-d) lattice polymer where each unit can exist in the cis or trans state, the stretched conformation corresponding to the all-trans state. We am only local conformational changes that do not perturb the chain beyond a small finite range. The mechanism of contraction then becomes the diffusion of cis states into the chain from the ends. Because of the diffusion mechanism we expect power-law behavior of the form t1/2 (this form is supported by exactly soluble models). We give exact series for short chains and the asymptotic series for very long chains. We find that the t1/2 behavior is truly asymptotic and does not dominate the early behavior as determined by the series.
引用
收藏
页码:235 / 247
页数:13
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