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Single Crystal Sub-Nanometer Sized Cu6(SR)6 Clusters: Structure, Photophysical Properties, and Electrochemical
Xiaohui Gao1, Shuijian He2, Chunmei Zhang1
1State Key Laboratory of Electroanalytical Chemistry Institution Changchun institute of Applied Chemistry Chinese Academy of Sciences 5625 Renmin Street Changchun 130022 Jilin China; University of Chinese Academy of Sciences 100039 Beijing China.
Abstract:
Organic ligand-protected metal nanoclusters have attracted extensively attention owing to their atomically precise composition, determined atom-packing structure and the fascinating properties and promising applications. To date, most research has been focused on thiol-stabilized gold and silver nanoclusters and their single crystal structures. Here the single crystal copper nanocluster species (Cu6(SC7H4NO)6) determined by X-ray crystallography and mass spectrometry is presented. The hexanuclear copper core is a distorted octahedron surrounded by six mercaptobenzoxazole ligands as protecting units through a simple bridging bonding motif. Density functional theory (DFT) calculations provide insight into the electronic structure and show the cluster can be viewed as an open-shell nanocluster. The UV-vis spectra are analyzed using time-dependent DFT and illustrates high-intensity transitions involving primarily ligand states. Furthermore, the as-synthesized copper clusters can serve as promising nonenzymatic sensing materials for high sensitive and selective detection of H2O2.
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