Scattering Neutrons along the Polyelectrolyte Complex/Coacervate Continuum

被引:60
作者
Fares, Hadi M. [1 ]
Ghoussoub, Yara E. [1 ]
Delgado, Jose D. [1 ]
Fu, Jingcheng [1 ]
Urban, Volker S. [2 ]
Schlenoff, Joseph B. [1 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
[2] Oak Ridge Natl Lab, Ctr Struct Mol Biol, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
BOVINE SERUM-ALBUMIN; COMPLEX COACERVATION; INTERFACIAL ENERGY; AQUEOUS-SOLUTIONS; LIGHT-SCATTERING; SALT; MULTILAYERS; CONFORMATION; DIFFUSION; SANS;
D O I
10.1021/acs.macromol.8b00699
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The coil size of narrow molecular weight distribution deuterated poly(styrenesulfonate), PSS, within a polyelectrolyte complex doped with KBr was tracked across the continuum from solid to coacervate to solution using small-angle neutron scattering. While PSS alone in solution exhibited the familiar and pronounced "polyelectrolyte effect" of coil shrinkage with increasing [KBr], the radius of gyration R-g of the PSS in the complex remained surprisingly constant up to 1.4 M KBr, which is close to the transition between complex and coacervate behavior. Thereafter, R-g decreased with increasing KBr, remaining slightly larger than R-g for PSS in KBr alone. Upturns in the scattering at low angle, seen for complexes in lower [KBr], are consistent with porosity, observed macroscopically as whitening of the bulk complex-a universal property of polyelectrolyte complexes. Reasons for this porosity, imaged by scanning electron microscopy, are discussed. At high q ranges, a correlation peak between deuterated coils of PSS was observed.
引用
收藏
页码:4945 / 4955
页数:11
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