Diphenyl(1-pyridyl)phosphine sulfide as a ligand in mono- and binuclear coinage metal complexes

M. Elena Olmos, Annette Schier, Hubert Schmidbaur

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Diphenyl(1-pyridyl)phosphine sulfide, Ph2pyPS, 1, gives a 1:1 complex (2) with AuCl upon treatment with (C4H8S)AuCl. According to an X-ray diffraction analysis, this compound is isomorphous with the Ph3PS complex. [Ph3PAu]BF4 and 1 give the cationic complex [Ph3PAuSPPyPh2]BF4 (3). With two equivalents of the same reagent the binuclear complex 4 is generated, in which the metal atoms are S- and N-bonded. The reaction of 2 equivalents of 1 with [(tetrahydrothiophene)2Au]ClO4 affords the 2:1 complex 5 with the gold atom exclusively S-bonded. The analogous reaction with AgBF4 gives the 2:1 complex 6, the structure of which has also been determined by X-ray diffraction. The silver atom is engaged in coordinative bonding with both sulfur and both nitrogen atoms in a quasi-tetrahedral environment. Addition of AgClO4 to compound 5, and of [(MeCN)4Cu]BF4 to 6, gives mixed-metal complexes (7, 8) with head-to-head structures, the silver atoms being exclusively S-bonded.

Original languageEnglish
Pages (from-to)385-390
Number of pages6
JournalZeitschrift fur Naturforschung - Section B Journal of Chemical Sciences
Volume52
Issue number3
DOIs
StatePublished - Mar 1997
Externally publishedYes

Keywords

  • Ambidentate Ligand
  • Copper(I)
  • Diphenyl(1-pyridyl)phosphine Sulfide
  • Goid(I) Coordination
  • Silver(I)

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