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Reaction of Tetracopper(I)-Phosphonitocavitand with PhSeSiMe3: Synthesis and Structure of a Polyanionic Cluster [pyH]6[(CuCl)9(μ3-SePh)5(μ4-SePh)]
Authors:Qian-Feng Zhang  Yu-Jie Liu  Richard D. Adams  Alexander Rothenberger  Dieter Fenske  Wa-Hung Leung
Affiliation:1. Department of Applied Chemistry, Anhui University of Technology, Maanshan, Anhui, 243002, P.R. China
2. Department of Chemistry and Biochemistry and the USC Nanocenter, University of South Carolina, Columbia, SC, 29208, USA
3. Institut für Anorganische Chemie, Universit?t Karlsruhe (TH), 76128, Karlsruhe, Germany
4. Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, P.R. China
Abstract:Treatment of tetracopper(I)-phosphonitocavitand [1·Cu4(μ-Cl)44-Cl)] (2) (1 = tetraphosphonitocavitand [rccc-2,8,14,20-tetrakis-(iso-butyl)-phosphonitocavitand (C44H48O8P4Ph4)]) with PhSeSiMe3 in THF at low temperature afforded a novel polyanionic cluster [pyH]6[(CuCl)93-SePh)54-SePh)] (4) as a major product along with a new tetracopper(I)-phosphonitocavitand (3) with a centered μ3-Cl. Molecular structure of anionic cluster in 4 consists of six PhSe bridging ligands containing five μ3-SePh and one exceptional μ4-SePh bridging nine copper atoms, of which eight copper atoms have trigonal coordination geometry and the other has distorted tetrahedral geometry. Dedicated to Professor Han-Qin Liu on the occasion of his 70th birthday.
Keywords:Copper(I)  phosphonitocavitand  copper–  selenium cluster  crystal structure  supramolecular chemistry
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