Nickel(0) stilbene complexes and the structure of bis(tri-p-tolylphosphine)(trans-stilbene)nickel(0) hemitetrahydrofuranate

Steven D. Ittel*, James A Ibers

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

A series of nickel(0)-stilbene complexes has been prepared by the reaction of triarylphosphines or tert-butyl isocyanide with bis(1,5-cyclooctadiene)nickel(0) in hexane. The structure of the complex bis(tri-p-tolylphosphine)(trans-stilbene)nickel(0) hemitetrahydrofuranate, Ni[P(C6H4CH3)3]2[(C6H5)HCCH(C6H5)] · 0.5(C4H8O), has been determined at room temperature from three-dimensional X-ray data collected by counter methods. The structure has been refined by least-squares techniques to a final R index (on F) of 0.092 based on 2417 observations above background. The material crystallizes in the orthorhombic space group D102h-Pccn, with eight molecules of complex and four molecules of solvent in a cell of dimensions a = 19.548(8), b = 26.145(12), c = 19.718(9) ». The Ni atom has trigonal coordination if the olefin is regarded as a monodentate ligand. The five atoms of the inner coordination sphere are distorted planar and the two olefinic carbon atoms are essentially equidistant from the nickel atom. The structure is compared with that of bis(tri-p-tolylphosphine)(azobenzene)nickel(0) determined previously. Observed differences in the bonding of the olefin and the isoelectronic azo complex are discussed.

Original languageEnglish (US)
Pages (from-to)121-134
Number of pages14
JournalJournal of Organometallic Chemistry
Volume74
Issue number1
DOIs
StatePublished - Jul 16 1974

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

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