堆积
范德瓦尔斯力
自组装
非共价相互作用
材料科学
二亚胺
分子
均苯四甲酸二酐
共轭体系
纳米纤维
超分子化学
聚合物
化学工程
纳米技术
表征(材料科学)
化学
氢键
有机化学
聚酰亚胺
复合材料
苝
图层(电子)
作者
Chiara Musumeci,Monika Wałęsa-Chorab,Adam Gorczyński,Grzegorz Markiewicz,Andrzej Bogucki,Roman Świetlik,Zbigniew Hnatejko,Wojciech Jankowski,Marcin Hoffmann,Emanuele Orgiu,Artur R. Stefankiewicz,Violetta Patroniak,Artur Ciesielski,Paolo Samorì
出处
期刊:ACS omega
[American Chemical Society]
日期:2017-04-26
卷期号:2 (4): 1672-1678
被引量:3
标识
DOI:10.1021/acsomega.7b00286
摘要
Small π-conjugated molecules can be designed and synthesized to undergo controlled self-assembly forming low-dimensional architectures, with programmed order at the supramolecular level. Such order is of paramount importance because it defines the property of the obtained material. Here, we have focused our attention to four pyromellitic diimide derivatives exposing different types of side chains. The joint effect of different noncovalent interactions including π-π stacking, H-bonding, and van der Waals forces on the four derivatives yielded different self-assembled architectures. Atomic force microscopy studies, corroborated with infrared and nuclear magnetic resonance spectroscopic measurements, provided complementary multiscale insight into these assemblies.
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