Electrochemical deposition of N-heterocyclic carbene monolayers on metal surfaces

Einav Amit(Hebrew University of Jerusalem), Linoy Dery(Hebrew University of Jerusalem), Shahar Dery(Hebrew University of Jerusalem), Suhong Kim(University of California, Berkeley), Anirban Roy(Bruker (United States)), Qichi Hu(Bruker (United States)), Vitaly Gutkin(Hebrew University of Jerusalem), Helen R. Eisenberg(Hebrew University of Jerusalem), Tamar Stein(Hebrew University of Jerusalem), Daniel Mandler(Hebrew University of Jerusalem), F. Dean Toste(University of California, Berkeley), Elad Gross(Hebrew University of Jerusalem)
Nature Communications
November 11, 2020
Cited by 76Open Access
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Abstract

Abstract N -heterocyclic carbenes (NHCs) have been widely utilized for the formation of self-assembled monolayers (SAMs) on various surfaces. The main methodologies for preparation of NHCs-based SAMs either requires inert atmosphere and strong base for deprotonation of imidazolium precursors or the use of specifically-synthesized precursors such as NHC(H)[HCO 3 ] salts or NHC–CO 2 adducts. Herein, we demonstrate an electrochemical approach for surface-anchoring of NHCs which overcomes the need for dry environment, addition of exogenous strong base or restricting synthetic steps. In the electrochemical deposition, water reduction reaction is used to generate high concentration of hydroxide ions in proximity to a metal electrode. Imidazolium cations were deprotonated by hydroxide ions, leading to carbenes formation that self-assembled on the electrode’s surface. SAMs of NO 2 -functionalized NHCs and dimethyl-benzimidazole were electrochemically deposited on Au films. SAMs of NHCs were also electrochemically deposited on Pt, Pd and Ag films, demonstrating the wide metal scope of this deposition technique.


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