Synthesis, coordination chemistry and crystal structures of [2+2] macrocycles incorporating 2,6-bis(thiomethyl)pyridine sub-units

Edwin C. Constable, Adam C. King, Paul R. Raithby

Research output: Contribution to journalArticlepeer-review

22 Citations (SciVal)

Abstract

A series of potentially dinucleating [2+2] macrocyclic ligands with two SNS metal-binding domains separated by a variable polymethylene chain have been prepared. Two examples of these ligands have been structurally characterised. These ligands form polymeric adducts with [Rh2(O2CCMe3)4] in which the ligands are thought to act as exocyclic S-donors to the axial sites of the dinuclear complex. In contrast, reaction with [(CO)2Rh(μ-Cl)2Rh(CO)2] resulted in the formation of dinuclear complexes in which two Rh(CO) units are bound to each macrocyclic ligand.

Original languageEnglish
Pages (from-to)4275-4289
Number of pages15
JournalPolyhedron
Volume17
Issue number23-24
DOIs
Publication statusPublished - 13 Nov 1998

Funding

—We gratefully acknowledge the Schweizerischer Nationalfonds zur Förderung der wissenenschaftlichen Forschung and EPSRC (U.K.) for support.

Keywords

  • Macrocycles
  • Rhodium complexes
  • Synthesis
  • X-ray structure

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

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