Role of O,C,O-ligand in a new coordination mode of organotin compounds to 2-mercapto-1-methylimidazol. Stabilization of its thione form
Název česky | Úloha O,C,O-ligandu v novem koordinačním typu organocinovych sloučenin s 2-merkapto-1-metylimidazolem a jeho stabilizace v thio-sormě |
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Autoři | |
Rok publikování | 2007 |
Druh | Článek v odborném periodiku |
Časopis / Zdroj | Journal of Organometallic Chemistry |
Fakulta / Pracoviště MU | |
Citace | |
Obor | Anorganická chemie |
Klíčová slova | OCO ligand coordination mode organotin compound stabilization thione form |
Popis | 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. |
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