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Structure and in vitro antifungal activity of [2,6‐bis(dimethylaminomethyl)phenyl]diphenyltin(IV) compounds
Authors:Ale&#x; Ric&#x;ka  Libor Dostl  Roman Jambor  Vladimír Buchta  Jir&#x;í Brus  Ivana Císar&#x;ov  Michal Holc&#x;apek  Jaroslav Holec&#x;ek
Institution:Ale? R??ic?ka,Libor Dostál,Roman Jambor,Vladimír Buchta,Jir?í Brus,Ivana Císar?ová,Michal Holc?apek,Jaroslav Holec?ek
Abstract:A set of seven 2,6‐bis(dimethylaminomethyl)phenyl]diphenyltin(IV) ({(CH3)2NCH2]2(C6H3)}­(C6H5)2Sn+X?) ionic organotin(IV) compounds (X = Br, NO3, CN, SCN, SeCN, BF4 and PF6) has been prepared and characterized by electrospray ionization mass spectrometry, 1H NMR spectroscopy in CDCl3,119Sn NMR in CDCl3 and DMSO‐d6 solution, as well as by 13C and 119Sn CP/MAS NMR spectroscopy and X‐ray diffraction techniques in the solid state. The in vitro antifungal activity of these water‐soluble ionic organotin(IV) compounds was compared with starting compounds and the antifungal drugs currently in clinical use. Copyright © 2002 John Wiley & Sons, Ltd.
Keywords:water‐soluble organotin(IV) compounds  N  C  N‐ligand  NMR spectroscopy  CP/MAS NMR spectroscopy  X‐ray diffraction  ESI mass spectrometry  in vitro antifungal screening
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