Role of O,C,O-ligand in a new coordination mode of organotin compounds to 2-mercapto-1-methylimidazol. Stabilization of its thione form

Investor logo

Warning

This publication doesn't include Faculty of Education. It includes Faculty of Informatics. Official publication website can be found on muni.cz.
Authors

MARTINCOVA Jana DOSTAL Libor TARABA Jan JAMBOR Roman

Year of publication 2007
Type Article in Periodical
Magazine / Source Journal of Organometallic Chemistry
MU Faculty or unit

Faculty of Informatics

Citation
Field Inorganic chemistry
Keywords OCO ligand coordination mode organotin compound stabilization thione form
Description The reaction of the organotin compound [Ph2LSn](+) [OTf](-) (1), (L(O,C,O) = 2,6-(t-BuOCH2)(2)C6H3), with the sodium salt Na(mimt), mimt = 1-methylimidazole-2-thiolate, resulted in the isolation of Ph2LSn(mimt) (2), where the polar group (mimt) has been stabilized as the thione-tautomeric form by the triorganotin fragment Ph2LSn. Product 2 was characterized by H-1, C-13 and Sn-119 NMR and IR spectroscopy, ESI/MS, elemental analyses and X-ray diffraction.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.