Chemically Interrogating N-Heterocyclic Carbenes at the Single-Molecule Level Using Tip-Enhanced Raman Spectroscopy
Source abstract
Abstract
N-heterocyclic carbenes (NHCs) have been established as powerful modifiers to functionalize metal surfaces for a wide variety of energy and nanoelectronic applications. To fundamentally understand and harness NHC modification, it is essential to identify suitable methods to interrogate NHC surface chemistry at the spatial limit. Here, we demonstrate tip-enhanced Raman spectroscopy (TERS) as a promising tool for chemically probing the surface properties of NHCs at the single-molecule scale. We show that with subnanometer resolution, TERS measurements are capable of not only unambiguously identifying the chemical structure of individual NHCs by their vibrational fingerprints but also definitively determining the binding mode of NHCs on metal surfaces. In particular, by investigating low-temperature NHC adsorption on Ag(111), our TERS studies provide insights into the temperature dependence of the adsorption properties of NHCs. This work suggests the potential of single-molecule vibrational spectroscopy for investigations of NHC surface modification at the most fundamental level.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: N-Heterocyclic Carbenes in Organic and Inorganic Chemistry · Catalytic Cross-Coupling Reactions · Asymmetric Hydrogenation and Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Illinois Chicago, Chicago, Illinois 60607, United States
Department of Physics and Astronomy, California State University, Northridge, Northridge, California 91330-8268, United States
Department of Physics, University of Illinois Chicago, Chicago, Illinois 60607, United States
Funding
Division of Chemistry · Division of Materials Research
References (42)
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