Physical Chemistry

Highly ordered N-heterocyclic carbene monolayers on Cu(111)

Authors

Abstract

The benzannulated N-heterocyclic carbene, 1,3-dibenzylbenzimidazolylidene (NHCDBZ) forms large, highly ordered domains when adsorbed on a Cu(111) surface under ultrahigh vacuum conditions. A combination of scanning tunneling microscopy (STM), high resolution electron energy loss spectroscopy (HREELS) and density functional theory (DFT) calculations reveals that the overlayer consists of vertical benzannulated NHC moieties coordinating to Cu adatoms. Long range order results from the placement of the two benzyl units from a single NHC on opposite sides of the benzimidazole moiety, with the planes of their aromatic rings approximately parallel to the surface. The organization of three surface-bound benzyl substituents from three different NHCs into a triangular array controls the formation of a highly ordered Kagome-like lattice on the surface. This study illustrates the importance of dispersive interactions to control the binding geometry and self-assembly of the NHC.

Content

Thumbnail image of Sep_09_2021_DBZ_Manuscript.pdf

Supplementary material

Thumbnail image of Sep_09_2021_DBZ_Manuscript_SI.pdf
Supporting Information
Synthetic details for NHC-DBZ, supplementary STM images and analysis, supplementary HREELS plots and details for DFT calculation methods.