Alkylzirconium-(III) and alkylzirconium-(IV) complexes
Identifiers
Permanent link (URI): http://hdl.handle.net/10017/4791DOI: 10.1016/0022-328X(85)80268-0
ISSN: 0022-328X
Publisher
Elsevier
Date
1985Bibliographic citation
Journal of Organometallic Chemistry, 1985, v. 295, p. 159-165
Keywords
Alkylzirconium-(III)
Alkylzirconium-(IV)
Project
2001/83 (Comisión Asesora de Investigación Científica y Técnica)
Document type
info:eu-repo/semantics/article
Version
info:eu-repo/semantics/publishedVersion
Publisher's version
http://dx.doi.org/10.1016/0022-328X(85)80268-0Rights
(c) Elsevier, 1985
Access rights
info:eu-repo/semantics/openAccess
Abstract
The complex [(η5-C5H5)2ZrCl]2 is oxidized by acetylenes PhCCR (R = H, Ph) to give dimeric alkenediylzirconium(IV) derivatives and can be methylated with LiMe and AlMe3. The methyl complex obtained in the reaction with LiMe is a diamagnetic solid characterized as [(η5-C5H5)ZrMe]2 by 1H NMR spectroscopy. This compound is reversibly acylated by CO, and the equilibrium can be displaced by simultaneous oxidation to give the η2-acetylzirconium(IV) complex [(η5- C5H5)2Zr(η5-COMe)]2(μ-O) The analogous insertion of CyNC (Cy = cyclohexyl) goes to completion, and the resulting diamagnetic dimer [(η5C5H5)2Zr(η2- CMeNCy)]2 has been characterized by IR and NMR spectroscopy. The methyl- zirconium(III) complex is a strong reducing agent, being oxidized by AgClO4 with deposition of metallic silver and by I2 to give (η5-C5H5 and (η5-C5H5)2ZrIMe.
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