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In Situ Formation of N-Heterocyclic Carbene-Bound Single-Molecule Junctions
Author(s) -
Evan A. Doud,
Michael S. Inkpen,
Giacomo Lovat,
Enrique Montes,
Daniel W. Paley⧓,
Michael L. Steigerwald,
Héctor Vázquez,
Latha Venkataraman,
Xavier Roy
Publication year - 2018
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.8b05184
Subject(s) - chemistry , molecule , conductance , nanoelectronics , break junction , monolayer , scanning tunneling microscope , nanotechnology , quantum tunnelling , density functional theory , electrochemistry , electrode , carbene , characterization (materials science) , molecular electronics , electron transport chain , metal , chemical physics , cyclic voltammetry , computational chemistry , catalysis , optoelectronics , materials science , organic chemistry , biochemistry , mathematics , combinatorics
Self-assembled monolayers (SAMs) formed using N-heterocyclic carbenes (NHCs) have recently emerged as thermally and chemically ultrastable alternatives to those formed from thiols. The rich chemistry and strong σ-donating ability of NHCs offer unique prospects for applications in nanoelectronics, sensing, and electrochemistry. Although stable in SAMs, free carbenes are notoriously reactive, making their electronic characterization challenging. Here we report the first investigation of electron transport across single NHC-bound molecules using the scanning tunneling microscope-based break junction (STM-BJ) technique. We develop a series of air-stable metal NHC complexes that can be electrochemically reduced in situ to form NHC-electrode contacts, enabling reliable single-molecule conductance measurements of NHCs under ambient conditions. Using this approach, we show that the conductance of an NHC depends on the identity of the single metal atom to which it is coordinated in the junction. Our observations are supported by density functional theory (DFT) calculations, which also firmly establish the contributions of the NHC linker to the junction transport characteristics. Our work demonstrates a powerful method to probe electron transfer across NHC-electrode interfaces; more generally, it opens the door to the exploitation of surface-bound NHCs in constructing novel, functionalized electrodes and/or nanoelectronic devices.

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