Intensely Luminescent Homoleptic Alkynyl Decanuclear Gold(I) Clusters and Their Cationic Octanuclear Phosphine Derivatives

Tutkimustuotos: Lehtiartikkeli


  • Igor O. Koshevoy
  • Yuh-Chia Chang
  • Antti Karttunen

  • Stanislav I. Selivanov
  • Janne Janis
  • Matti Haukka
  • Tapani A. Pakkanen
  • Sergey P. Tunik
  • Pi-Tai Chou


  • University of Eastern Finland
  • National Taiwan University
  • St. Petersburg State University


Treatment of Au(SC4H8)Cl with a stoichiometric amount of hydroxyaliphatic alkyne in the presence of NEt3 results in high-yield self-assembly of homoleptic clusters (AuC2R)(10) (R = 9-fluorenol (1), diphenylmethanol (2), 2,6-dimethyl-4-heptanol (3), 3-methyl-2-butanol (4), 4-methyl-2-pentanol (4), 1-cyclohexanol (6), 2-borneol (7)). The molecular compounds contain an unprecedented catenane metal core with two interlocked 5-membered rings. Reactions of the decanuclear clusters 1-7 with gold-diphosphine complex [Au-2(1,4-PPh2-C6H4-PPh2)(2)](2+) lead to octanuclear cationic derivatives [Au-8(C2R)(6)(PPh2-C6H4-PPh2)(2)](2+) (8-14), which consist of planar tetranuclear units {Au-4(C2R)(4)} coupled with two fragments [AuPPh2-C6H4-PPh2(AuC2R)](+). The titled complexes were characterized by NMR and ESI-MS spectroscopy, and the structures of I, 13, and 14 were determined by single-crystal X-ray diffraction analysis. The luminescence behavior of both Au-10(I) and Au-8(I) families has been studied, revealing efficient room-temperature phosphorescence in solution and in the solid state, with the maximum quantum yield approaching 100% (2 in solution). DFT computational studies showed that in both Au-10(I) and Au-8(I) clusters metal-centered Au --> Au charge transfer transitions mixed with some pi-alkynyl MLCT character play a dominant role in the observed phosphorescence.


JulkaisuInorganic Chemistry
TilaJulkaistu - 2 heinäkuuta 2012
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

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