含苝聚酰亚胺分子内向列序通过链折叠的可能性:分子动力学研究

P.R. Sundararajan , G. Sacripante , Z.Y. Wang
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引用次数: 2

摘要

含苝主链聚酰亚胺是光电器件光电发生层的候选材料。这些聚合物在合成时是半结晶的。退火提高了结晶度,同时引起x射线衍射图的细微变化和紫外-可见吸收光谱的红移。Pe-C12-Pe -线性链的分子动力学模拟导致链折叠坍塌结构。众所周知,在线性烷烃的情况下,要发生稳定的折叠,至少需要150个CH2单位的链长。然而,苝之间强烈的吸引π相互作用导致链折叠,只有12个CH2间隔单元。这表明在这些体系中分子内和分子间的向列顺序都可以发生,前者是由链折叠引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The possibility of intra-molecular nematic order via chain folding in perylene-containing polyimides: a molecular dynamics study

Perylene containing main-chain polyimides are candidate materials for the photogenerator layer of electrophotographic devices. These polymers are semi-crystalline as synthesized. Annealing improves the crystallinity while causing subtle changes in the X-ray diffraction pattern and a red-shift in the UV–vis absorption spectrum. Molecular dynamics simulations of linear chains of …Pe–C12–Pe… led to chain folded collapsed structures. It is known that a minimum chain length of 150 CH2 units is required, in the case of linear alkanes, for stable folding to occur. However, the strong attractive π interaction between the perylene units causes the chain to fold, with as few as 12 CH2 spacer units. This shows that both intra and intermolecular nematic order can occur in these systems, the former caused by chain folding.

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