Self-assembled monolayers of N-heterocyclic carbenes (NHCs) on copper are reported. The monolayer structure is highly dependent on the N,N-substituents on the NHC. On both Cu(111) and Au(111), bulky isopropyl substituents force the NHC to bind perpendicular to the metal surface while methyl- or ethyl-substituted NHCs lie flat. Temperature-programmed desorption studies show that the NHC binds to Cu(111) with a desorption energy of E =152±10 kJ mol . NHCs that bind upright desorb cleanly, while flat-lying NHCs decompose leaving adsorbed organic residues. Scanning tunneling microscopy of methylated NHCs reveals arrays of covalently linked dimers which transform into adsorbed (NHC) Cu species by extraction of a copper atom from the surface after annealing.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765499 | PMC |
http://dx.doi.org/10.1002/cphc.201701045 | DOI Listing |
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