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分子共面性和分子内氢键促进的自组装。

Molecular Coplanarity and Self-Assembly Promoted by Intramolecular Hydrogen Bonds.

机构信息

Department of Chemistry, Texas A&M University , 3255 TAMU, College Station, Texas 77843, United States.

出版信息

Org Lett. 2016 Dec 16;18(24):6332-6335. doi: 10.1021/acs.orglett.6b03225. Epub 2016 Nov 30.

Abstract

Active conformational control is realized in a conjugated system using intramolecular hydrogen bonds to achieve tailored molecular, supramolecular, and solid-state properties. The hydrogen bonding functionalities are fused to the backbone and precisely preorganized to enforce a fully coplanar conformation of the π-system, leading to short π-π stacking distances, controllable molecular self-assembly, and solid-state growth of one-dimensional nano-/microfibers. This investigation demonstrates the efficiency and significance of an intramolecular noncovalent approach in promoting conformational control and self-assembly of organic molecules.

摘要

通过分子内氢键实现共轭体系中的动态构象控制,从而获得定制的分子、超分子和固态性质。氢键官能团融合到主链中,并经过精确的预组织,以强制实现π-体系的完全共面构象,从而导致短的π-π堆积距离、可控的分子自组装以及一维纳米/微纤维的固态生长。这项研究证明了分子内非共价作用在促进有机分子的构象控制和自组装方面的有效性和重要性。

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