分子动力学
Atom(片上系统)
化学物理
溶剂
自组装
动力学(音乐)
材料科学
化学
纳米技术
结晶学
计算化学
物理
计算机科学
并行计算
有机化学
声学
作者
Poyu Chen,Ching H. Wu,Pingping Wu,Chi‐Chung Hua
标识
DOI:10.1021/acs.jpcb.5c01940
摘要
Multistage self-assembly events of a high-performance bisurea (hexamethylene diisocyanate-benzylamine, HDI-BA) in a mixed-solvent medium (polyester/o-xylene = 1:1 in weight), wherein the polyester oligomer serves as a cooling agent to sufficiently slow down the solvent dynamics and thereby sustain the entire self-assembly process, are captured using united-atom molecular dynamics (UAMD) and coarse-grained molecular dynamics (CGMD) simulations. While the UAMD simulation captures the formation of primal bisurea chains via regular hydrogen bonding between folded HDI-BA molecules, the subsequent CGMD simulation provides compelling evidence of consecutive intertwining events of the HDI-BA chains that produce increasingly wider, stiffer, and more twisted fibrous objects mimicking the uniform and helical-like micrometer-fibers observed in recent experiments. Overall, this appears to be the first report revealing that bisurea may simultaneously capitalize on regular molecular packing in the initial stage and consecutive polymer-like intertwining in subsequent stages to foster highly regular self-assemblies with dimensions in the micrometer range.
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