电导
分子
酰胺
平面度测试
量子隧道
反应性(心理学)
材料科学
密度泛函理论
断开连接
脱质子化
光电子学
纳米技术
化学
化学物理
计算化学
结晶学
离子
有机化学
物理
凝聚态物理
病理
替代医学
医学
作者
Ming‐Zhu Huang,Qinghai Zhou,Feng Liang,Lei Yu,Bohuai Xiao,Yunchuan Li,Mingyang Zhang,Yan Chen,Jin He,Shengxiong Xiao,Shuai Chang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-06-14
卷期号:21 (12): 5409-5414
被引量:14
标识
DOI:10.1021/acs.nanolett.1c01882
摘要
Amides are essential in the chemistry of life. Detecting the chemical bond states within amides could unravel the nature of amide stabilization and planarity, which is critical to the structure and reactivity of such molecules. Yet, so far, no work has been reported to detect or measure the bond changes at the single-molecule level within amides. Here, we show that a transition between single and double bonds between N and C atoms in an amide can be monitored in real time in a nanogap between gold electrodes via the generation of distinctive conductance features. Density functional theory simulations show that the switching between amide isomers proceeds via a proton transfer process facilitated by a water molecule bridge, and the resulting molecular junctions display bimodal conductance states with a difference as much as nine times.
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