4.6 Article

Insight Into the Stability and Electronic and Optical Properties of N-Heterocyclic Carbene Analogues of Halogen/Phosphine-Protected Au13 Superatomic Clusters

期刊

JOURNAL OF PHYSICAL CHEMISTRY A
卷 126, 期 4, 页码 536-545

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpca.1c09084

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资金

  1. Chilean-French ECOSCONYCYT Program [C18E04]
  2. French Chilean International Associated Laboratory for Multifunctional Molecules and Materials (LIA-CNRS) [1027]
  3. GENCI (Grand Equipment National de Calcul Intensif) [a0010807367]
  4. China Scholarship Council
  5. Fondecyt [1180683]

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This study explores the feasibility of incorporating N-heterocyclic carbenes (NHCs) as part of the protecting-ligand shell in gold nanoclusters (AuNCs). The results show that the substitution of phosphine ligands with NHCs in experimentally characterized AuNCs demonstrates similar electronic structure and stability, but slightly different optical properties. These findings support the obtainment of novel targets for explorative synthesis efforts featuring NHC ligands on medium-sized species based on the recurrent Au-13 icosahedral core.
Atomically precise gold nanoclusters (AuNCs) belong to a relevant area oflering useful templates with tunable properties toward functional nanostructures. In this work, we explored the feasible incorporation of N-heterocyclic carbenes (NHCs), as part of the protecting-ligand shell in AuNCs. Our results, which are based on the substitution of phosphine ligands in experimentally characterized AuNCs by NHCs in various eight-electron superatoms Au-13 and M4Au9 (M = Cu, Ag), indicate similar electronic structure and stability but somewhat diflerent optical properties. These findings support the feasible obtention of novel targets for explorative synthetic eflorts featuring NHC ligands on medium-sized species based on the recurrent Au-13 icosahedral core. The hypothetical species appear to be interesting templates for building blocks in nanostructured materials with tuned properties, which encourage experimental exploration of ligand versatility in homo-and heterometallic superatomic clusters.

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