Remote and α-Thio Carbene Complexes Derived from an Oxazolinylsubstituted Thiophene

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 (2and 5) can be classified as a-thio or remote carbene com...

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Veröffentlicht in:Zeitschrift für Naturforschung. B, A journal of chemical sciences A journal of chemical sciences, 2012-06, Vol.67 (6), p.509-518
Hauptverfasser: Dobrzańska, Liliana, Julius, Gerrit R., Stander-Grobler, Elzet, Burger (neé Stander), Yolanda, Nogai, Stefan D., Cronje, Stephanie, Raubenheimer, Helgard G.
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Sprache:eng
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Zusammenfassung: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 (2and 5) can be classified as a-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.
ISSN:0932-0776
1865-7117
DOI:10.5560/znb.2012-0118