Affiliation:
1. Institut für Anorganische Chemie der Universität Würzburg
Abstract
The reaction of SbBr3 with the complex metal carbonyl anions [π-C5H6(CO)3M]Na (M = Mo, W) leads to the formation of transition metal antimony bromides π-C5H5(CO)3M-Sb̅-Br2, which can be further metallated, yielding the stable species
[XXX]
All bromine substituted transition metal stibines prove to be excellent coordinating ligands and can easily be introduced into activated metal carbonyls. The interaction of π-C5H5(CO)3M-Sb̅Br2, with bromine results in a quantitative Sb-M bond cleavage, presumably via primary formation of pentavalent intermediates. All new compounds are fully characterized by means of IR, 1H NMR and mass spectroscopy.
Cited by
17 articles.
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1. Synthesis, structure and reactivity of ferrio-chloro-phosphanes, -arsanes and -stibanes [(CO)2(η5-C5Me5)FePn(Cl)R] (Pn = P, As, Sb); R = tetramethylcyclopentadienyl, 2,7-di-tert-butylfluorenyl, 2,7-di-tert-butyl-9-trimethylsilylfluorenyl) as precursor to novel metallo-phosphaalkenes, -arsaalkenes, and -stibaalkenes;Dalton Trans.;2004
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4. Further synthetic and structural studies on cobalt carbonyl containing antimony complexes;Journal of Organometallic Chemistry;1992-06
5. Complexes with Substituent-free Acyclic and Cyclic Phosphorus, Arsenic, Antimony, and Bismuth Ligands;Angewandte Chemie International Edition in English;1990-10