Constructing multimetallic systems with the naphthalene-1,8-bis(thiolato) ligand

Stuart D. Robertson, Alexandra M. Z. Slawin, J. Derek Woollins

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Abstract

Addition of 1 equiv. (Ph3P)Au(ClO4) (formed by ion exchange of Ph3PAuCl with AgClO4) to [naphthalene-1,8-bis(thiolato)]bis (triphenylphosphane) platinum results in the formation of a novel dimetallic cationic complex with a (triphenylphosphane)gold moiety attached to the sulfur of the naphthalene-1,8-bis(thiolato) ligand. NMR spectroscopic evidence suggests that this gold-containing fragment is fluxional in its bonding and X-ray crystallography confirms the asymmetric complex, which shows this gold atom attached to one of these sulfur atoms. Addition of more than 1 equiv. (Ph3P)Au-(ClO4) results in the formation of a tetrametallic sandwich complex with two bridging gold atoms between the sulfur atoms of the two PtS2C3 rings. Tri- and tetrametallic silver-containing complexes can be prepared by addition of 0.5 and 1 equiv. AgClO4 to (Ph3P)(2)Pt(S2C10H6), respectively. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007.

Original languageEnglish
Pages (from-to)247-253
Number of pages7
JournalEuropean Journal of Inorganic Chemistry
Issue number2
DOIs
Publication statusPublished - Jan 2007

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Keywords

  • sulfur ligand
  • multimetallic systems
  • gold
  • bridging ligands
  • x-ray structure
  • electrospray mass-spectometry

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