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单动态共价键定制的响应性分子结

Single Dynamic Covalent Bond Tailored Responsive Molecular Junctions.

作者信息

Hu Yong, Li Jin, Zhou Yu, Shi Jie, Li Guopeng, Song Hang, Yang Yang, Shi Jia, Hong Wenjing

机构信息

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.

Shenzhen Research Institute of Xiamen University, Shenzhen, 518000, China.

出版信息

Angew Chem Int Ed Engl. 2021 Sep 13;60(38):20872-20878. doi: 10.1002/anie.202106666. Epub 2021 Aug 11.

Abstract

Responsive molecular devices are one of the core units for molecular electronics, and dynamic covalent bonds (DCBs) provide the opportunity for the fabrication of responsive molecular devices. Herein we employ a single dynamic acyl hydrazone bond to fabricate tailored molecular devices using the scanning tunneling microscopy break-junction technique (STM-BJ) and the eutectic Ga-In technique (EGaIn). We found that the single-DCB-tailored molecular devices exhibited acid-base and/or photo-thermal response with three well-defined molecular conductance states. The reversible switching has the ON/OFF ratio of ≈10 between each state for single-molecule junctions and ≈3 for the SAMs-based molecular junctions. Combined with the density functional theory calculations, we revealed that the multiple conductance states of these molecular junctions originate from the dynamic acyl hydrazone bond exchange and C=N isomerization. Our work opens the avenue towards the design of tailored single-molecule electrical devices by implanting dynamic covalent bonds in molecular architectures.

摘要

响应性分子器件是分子电子学的核心单元之一,动态共价键(DCB)为响应性分子器件的制造提供了契机。在此,我们利用单动态酰腙键,采用扫描隧道显微镜断接技术(STM-BJ)和共晶镓铟技术(EGaIn)来制造定制的分子器件。我们发现,单DCB定制的分子器件表现出酸碱和/或光热响应,具有三个明确的分子电导状态。对于单分子结,各状态之间的可逆开关的开/关比约为10,对于基于自组装单分子膜(SAMs)的分子结则约为3。结合密度泛函理论计算,我们揭示了这些分子结的多重电导状态源于动态酰腙键交换和C=N异构化。我们的工作为通过在分子结构中引入动态共价键来设计定制的单分子电子器件开辟了道路。

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