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Z. Naturforsch. 2012, 67b, 509 – 518
doi:10.5560/ZNB.2012-0118
Remote and α-Thio Carbene Complexes Derived from an Oxazolinyl-substituted Thiophene
Liliana Dobrzańska1,2, Gerrit R. Julius1, Elzet Stander-Grobler1, Yolanda Burger (neé Stander)3, Stefan D. Nogai1, Stephanie Cronje1,4, and Helgard G. Raubenheimer1
1 Department of Chemistry and Polymer Science, University of Stellenbosch, Private Bag X1, Matieland, 7602, Stellenbosch, South Africa
2 Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200F – bus 2404, B-3001 Heverlee, Belgium
3 Department of Chemistry, University of Johannesburg, P. O. Box 524, Auckland Park, 2006, Johannesburg, South Africa
4 Institut für Anorganische und Analytische Chemie, Johann Wolfgang Goethe-Universität Frankfurt, Max-von-Laue-Strasse 7, D-60348 Frankfurt am Main, Germany
Reprint requests to Prof. Helgard G. Raubenheimer. Fax: +27 21 8083849. E-mail: hgr@sun.ac.za
Received May 5, 2012 / published online July 6, 2012
Dedicated to Professor Wolfgang Beck on the occasion of his 80th birthday in recognition of his many contributions to inorganic and organometallic chemistry
Transmetallation and oxidative substitution were utilized to prepare examples of group 14, group 6 and group 10 complexes from lithiated or chlorinated 4,4-dimethyl-2-(2-thienyl) oxazoline or its N-alkylated analogs. Two of the product types (2 and 5) can be classified as α-thio or remote carbene complexes, depending on the position (3- or 5-) of attachment to the substituted thiophene ring. Spectroscopic measurements as well as crystal and molecular structure determinations clarified the bonding within the new compounds.
Key words: Carbene Complexes, Thienylidene Complexes, remote Carbenes, Chromium, Palladium
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