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分子尺度上具有偶氮苯中心桥的双齿配体的多功能开关。

Multi-functional switches of ditopic ligands with azobenzene central bridges at a molecular scale.

机构信息

Université de Paris, ITODYS, CNRS, UMR 7086, 15 rue J-A de Baïf, F-75013 Paris, France.

出版信息

Nanoscale. 2019 Dec 21;11(47):23042-23048. doi: 10.1039/c9nr06350a. Epub 2019 Nov 27.

Abstract

Ligands are designed to have ditopic bipyridine terminal groups linked through photochromic azobenzene central units, which exhibit multi-switchable properties by different external stimuli. The molecule can switch between cis-and trans-conformations at their bipyridine terminal groups upon protonation and at their central azobenzene units upon irradiation of photons. As a result, the system shows four different isomeric states: cis-TRANS, trans-TRANS, cis-CIS and trans-CIS. The four conformers are switched and are visualized by scanning tunneling microscopy at the solid-liquid interface, which gives a direct demonstration of the multi-functional switches at a molecular level.

摘要

配体设计为具有双吡啶端基的二齿配体,通过光致变色的偶氮苯中心单元连接,通过不同的外部刺激表现出多种可切换的性质。该分子可以在其双吡啶端基质子化时在顺式和反式构象之间切换,并且在其中心偶氮苯单元受到光子照射时切换。结果,该系统显示出四种不同的异构态:顺式-反式、反式-反式、顺式-顺式和反式-顺式。这四种构象通过在固液界面的扫描隧道显微镜进行切换和可视化,在分子水平上直接证明了多功能开关。

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