Abstract
Reactions of the complexes [Mol3(CO)2(?5-C5H5)] and [W(SC6F5)3(CO)(?5-C 5H5)] with M'(SC6F5) give Cs[Mo(SC6F5)4(?5-C 5H5)], M'[W(SC6F5)4(?5-C 5H5)] (M' = Cs, Rb or K) and solvated derivatives (M = Mo or W) M'[W(SC6F5)4(?5-C 5H5)]·nthf (M' = Li, n = 4; or Na, n = 1); 133Cs and 19F NMR studies of Cs[M(SC6F5)4(?5-C 5H5)] reveal co-ordination between the Cs+ and the organometallic anion and Cs-F coupling involving four o-fluorines of the SC6F5 groups, J(Cs-F) ˜ 58 Hz.
| Original language | English |
|---|---|
| Pages (from-to) | 2531-2532 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society, Dalton Transactions |
| Issue number | 16 |
| DOIs | |
| Publication status | Published - 1992 |
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Dive into the research topics of 'Co-ordination of alkali metals to sulfur-based organometallic ligands: 133Cs and 19F nuclear magnetic resonance studies of Cs[Mo(SC6F5)4(η5-C 5H5)], the first example of caesium-fluorine spin-spin coupling'. Together they form a unique fingerprint.Cite this
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