The Effect of Intramolecular Cross-Linking on Polymer Interactions in Solution

被引:19
|
作者
Galant, Or [1 ]
Davidovich-Pinhas, Maya [2 ]
Diesendruck, Charles E. [3 ]
机构
[1] Technion Israel Inst Technol, Interdept Program Polymer Engn, IL-3200003 Haifa, Israel
[2] Technion Israel Inst Technol, Biotechnol & Food Engn, IL-3200008 Haifa, Israel
[3] Technion Israel Inst Technol, Schulich Fac Chem, IL-3200003 Haifa, Israel
基金
以色列科学基金会;
关键词
critical concentration; entanglements; intramolecular collapse; rheology; solvent quality; SINGLE-CHAIN NANOPARTICLES; LONGEST RELAXATION-TIME; ORGANIC NANOPARTICLES; DISORDERED PROTEINS; VISCOSITY; RHEOLOGY; WATER; POLYELECTROLYTE; FRAGMENTATION; DEPENDENCE;
D O I
10.1002/marc.201800407
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 conformation of a polymer in a solvent is typically defined by the solvent quality, which is a consequence of the solvent and macromolecule's chemistry. Yet, additional factors can affect the polymer conformation, such as non-covalent interactions to surfaces or other macromolecules, affecting the amount of polymer-solvent interactions. Herein, chemically folded polymers with protein-like architectures are studied and compared to their unfolded linear precursor in good solvents using rheology measurements. The current research reveals that permanent folding by intramolecular chemical cross-linking limits the chain mobility and therefore causes a reduction in polymer-solvent interactions, making a good solvent become theta. This change not only affects the "solvent quality" but also leads to a change in particle-particle interactions as a function of concentration. These findings provide crucial insight into the effects of intramolecular cross-links on macromolecule solubility and self-assembly, which are critical for mimicking structurally similar biological materials.
引用
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页数:5
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