Transition metal complexes with sterically demanding ligands. I. Synthesis and X-ray crystal structure of 1,5-cyclooctadiene palladium methyl triflate, (COD)Pd(Me)(OTf) and its cationic penta-coordinate adducts with sterically demanding 2,9-diaryl-substituted 1,10-phenanthroline ligands
The synthesis, use and X-ray crystal structure of the novel cyclooctadiene Pd–triflate methyl complex 1 is described. Evidence for ionization of the triflate ligand in 1 in solution is presented through IR, 19F-NMR and conductivity measurements. The high reactivity of this starting material is exemp...
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Published in | Journal of organometallic chemistry Vol. 575; no. 2; pp. 214 - 222 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.03.1999
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Subjects | |
Online Access | Get full text |
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Summary: | The synthesis, use and X-ray crystal structure of the novel cyclooctadiene Pd–triflate methyl complex
1 is described. Evidence for ionization of the triflate ligand in
1 in solution is presented through IR,
19F-NMR and conductivity measurements. The high reactivity of this starting material is exemplified through the preparation of the novel cationic pentacoordinate Pd complexes
4 and
5, from
1 and the sterically demanding 2,9-diarylsubstituted 1,10-phenanthroline ligands
2 and
3. Complexes
4 and
5 have a pseudo-trigonal bipyramidal structure and display significant differences of the binding mode of the two olefin moieties of the cyclooctadiene ligand. This has been substantiated through
1H- and
13C-NMR spectroscopic data and for complex
4 by an X-ray crystallographic study. |
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ISSN: | 0022-328X 1872-8561 |
DOI: | 10.1016/S0022-328X(98)00997-8 |