Single chain polyelectrolyte conformation 1 - Influence of the spatial dimension and ionic strength

被引：0

作者：

Irurzun, IM ^{[1
]}

Matteo, CL ^{[1
]}

机构：

[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Fis, RA-1428 Buenos Aires, Argentina

来源：

MACROMOLECULAR THEORY AND SIMULATIONS | 2001年 / 10卷 / 04期

关键词：

D O I：

10.1002/1521-3919(20010401)10:4<237::AID-MATS237>3.0.CO;2-V

中图分类号：

O63 [高分子化学（高聚物）];

学科分类号：

070305 ; 080501 ; 081704 ;

摘要：

Single polyelectrolyte chains were simulated in the Debye-Huckel approximation. The average end-to-end quadratic distance (R-2) was calculated as a function pf the chain length, the ionic strength of the solution and the dimension of space. The upper critical dimension d = 6, for the electrostatic interaction, and the asymptotic Stretched behavior are in agreement with recent developments of renormalization group theory. The transition between stretched and coiled conformations is described.

引用

页码：237 / 243

页数：7

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