Abstract
New bimetallic complexes [MTl(SC6F5)2L2Cp] (L = SC6F5, M = Mo (1a), W (1b); L = CO, M = Mo (4)) are characterised; crystal structures of 1a and 4 show unusual polydentate coordination of thallium(I) by [Mo(SC6F5)2L2Cp)]- and var. temp. 19F NMR studies, supported by conductivity measurements and cation exchange, indicate restricted rotation of C6F5 groups and reversible decoordination of Tl+ in more polar solvents. © 1987.
| Original language | English |
|---|---|
| Pages (from-to) | C1-C6 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 322 |
| Issue number | 1 |
| Publication status | Published - 17 Mar 1987 |
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Dive into the research topics of 'Cyclopentadienyl pentafluorophenylthiolate complexes of molybdenum and tungsten as novel polydentate ligands of thallium(I); dynamic NMR studies and crystal structures of two derivatives [MoTl(SC6F5)2L2Cp] (L = SC6F5 or CO)'. Together they form a unique fingerprint.Cite this
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