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A Resilient Platform for the Discrete Functionalization of Gold Surfaces Based on N-Heterocyclic Carbene Self-Assembled Monolayers

Joseph M. Palasz, Zhuoran Long, Jinhui Meng, Pablo E. Videla, H. Ray Kelly, Tianquan Lian, Víctor S. Batista, Clifford P. Kubiak

2024Journal of the American Chemical Society12 citationsDOIOpen Access PDF

Abstract

We describe the synthesis and characterization of a versatile platform for gold functionalization, based on self-assembled monolayers (SAMs) of distal-pyridine-functionalized N-heterocyclic carbenes (NHC) derived from bis(NHC) Au(I) complexes. The SAMs are characterized using polarization-modulation infrared reflectance-absorption spectroscopy, surface-enhanced Raman spectroscopy, and X-ray photoelectron spectroscopy. The binding mode is examined computationally using density functional theory, including calculations of vibrational spectra and direct comparisons to the experimental spectroscopic signatures of the monolayers. Our joint computational and experimental analyses provide structural information about the SAM binding geometries under ambient conditions. Additionally, we examine the reactivity of the pyridine-functionalized SAMs toward H 2 SO 4 and W(CO) 5 (THF) and verify the preservation of the introduced functionality at the interface. Our results demonstrate the versatility of N-heterocyclic carbenes as robust platforms for on-surface acid–base and ligand exchange reactions.

Topics & Concepts

ChemistryMonolayerSurface modificationCarbeneRaman spectroscopyDensity functional theoryX-ray photoelectron spectroscopyReactivity (psychology)Self-assembled monolayerPyridineInfrared spectroscopyAbsorption spectroscopyPhotochemistryCombinatorial chemistryComputational chemistryPhysical chemistryOrganic chemistryChemical engineeringMedicineEngineeringAlternative medicineOpticsPathologyQuantum mechanicsCatalysisPhysicsBiochemistryMolecular Junctions and NanostructuresCatalytic Cross-Coupling ReactionsN-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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