Melts of nonconcatenated rings in spherical confinement

被引:11
|
作者
Pachong, Stanard Mebwe [1 ]
Chubak, Iurii [2 ]
Kremer, Kurt [1 ]
Smrek, Jan [2 ]
机构
[1] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[2] Univ Vienna, Fac Phys, Boltzmanngasse 5, A-1090 Vienna, Austria
来源
JOURNAL OF CHEMICAL PHYSICS | 2020年 / 153卷 / 06期
基金
欧洲研究理事会; 美国国家科学基金会; 奥地利科学基金会;
关键词
TOPOLOGICAL CONSTRAINTS; POLYMER; DYNAMICS; CONFORMATIONS; RHEOLOGY; MODEL;
D O I
10.1063/5.0013929
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Motivated by the chromosomes enclosed in a cell nucleus, we study a spherically confined system of a small number of long unknotted and nonconcatenated polymer rings in a melt and systematically compare it with the bulk results. We find that universal scaling exponents of the bulk system also apply in the confined case; however, certain important differences arise. First, due to confinement effects, the static and threading properties of the rings depend on their radial position within the confining sphere. Second, the rings' dynamics is overall subdiffusive, but anisotropic along the directions parallel and perpendicular to the sphere's radius. The radial center of mass displacements of the rings are in general much smaller than the angular ones, which is caused by the confinement-induced inhomogeneous radial distribution of the whole rings within the sphere. Finally, we find enhanced contact times between rings as compared to the bulk, which indicates slow and predominantly coordinated pathways of the relaxation of the system.
引用
收藏
页数:12
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