Reactivity Variance Between Stereoisomers of Saturated N-heterocyclic Carbenes on Gold Surfaces

Controlling the chirality of molecule-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 symmetric and one Cs symmetric, of saturated N-heterocyclic carbenes (NHCs) and a structurally related unsaturated NHC (C2v symmetric) 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. Theoretical 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-symmetric NHC to a formal elimination of H2, while the C2-symmetric 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. Two stereoisomers, one C2 symmetric and one Cs symmetric, of saturated N-heterocyclic carbenes (NHCs) were placed on gold films and they demonstrate different reactivity.