Products Cited in Publications Worldwide Reactivity variance between stereoisomers of saturated N-heterocyclic carbenes on gold surfaces

Reactivity variance between stereoisomers of saturated N-heterocyclic carbenes on gold surfaces

Kaur, Gurkiran; Dominique, Nathaniel L.; Hu, Gaohe; Nalaoh, Phattananawee; Thimes, Rebekah L.; Strausser, Shelby L.; Jensen, Lasse; Camden, Jon P.; Jenkins, David M.

DOI:

Abstract

Controlling the chirality of mol.-surface systems is essential for applications ranging from heterogeneous catalysis to biosensing. N-heterocyclic carbenes (NHCs) are quickly becoming a dominant ligand for noble metal surface passivation, but the potential of chiral NHC scaffolds remains untapped. In this work, two stereoisomers, one C2 sym. and one Cs sym., of saturated N-heterocyclic carbenes (NHCs) and a structurally related unsaturated NHC (C2v sym.) were synthesized as NHC-CO2 adducts. These CO2-protected NHCs were deposited on gold films and their presence on the films was confirmed by laser desorption ionization mass spectrometry (LDI-MS) and surface enhanced Raman spectroscopy (SERS). Surprisingly, the Cs NHC, but not the chiral C2 NHC, partially degrades to the independently synthesized unsaturated NHC upon binding to the gold. Theor. calculations assist in explaining this phenomenon by showing that the NHCs primarily lie flat on the gold surfaces, which exposes the backbone protons on the Cs-sym. NHC to a formal elimination of H2, while the C2-sym. NHC remains protected from this elimination reaction. These results raise critical questions as to how the structure of NHC ligands may be tuned to influence binding and reactivity on gold surfaces.

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