| Literature DB >> 34254414 |
Yong Hu1, Jin Li1, Yu Zhou1, Jie Shi1, Guopeng Li1, Hang Song1, Yang Yang1, Jia Shi1, Wenjing Hong2.
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.Entities:
Keywords: Dynamic covalent chemistry; acyl hydrazone bond; molecular junction; responsive molecular device; scanning tunneling microscopy break-junction technique
Year: 2021 PMID: 34254414 DOI: 10.1002/anie.202106666
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336