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 language | English |
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Pages (from-to) | 4275-4289 |
Number of pages | 15 |
Journal | Polyhedron |
Volume | 17 |
Issue number | 23-24 |
DOIs | |
Publication status | Published - 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