Login for students

Login for employees

Publication detail

Structure of azo dye organotin(IV) compounds containing a C,N-chelating ligand, part II, and their in vitro antifungal activity
Authors: Novák Petr | Lyčka Antonín | Císařová Ivana | Buchta Vladimír | Silva Luis | Kolářová Lenka | Růžička Aleš | Holeček Jaroslav
Year: 2005
Type of publication: článek v odborném periodiku
Name of source: Applied Organometallic Chemistry
Publisher name: John Wiley & Sons Ltd.
Place: Chichester
Page from-to: 500-509
Titles:
Language Name Abstract Keywords
cze Structure of azo dye organotin(IV) compounds containing a C,N-chelating ligand, part II, and their in vitro antifungal activity Eight complexes of azo dyes used in routine industrial processes and the [(2-dimethylaminomethyl) phenyl](R-2)tin(IV) moiety (R = Ph or n-Bu) have been prepared, their NMR, electrospray ionization mass spectrometry, IR and UV-VIS spectra measured, and the X-ray structure of ([2-(N,N-dimethylaminomethyl)phenyl](diphenyl))tin(IV)-2-{[N'-(2-oxo-1-phenylcarbamoylpropyliden)hydrazo]}benzoate (3a), determined. The compounds reveal similar structures in chloroform solution (NMR) and in the solid state (X-ray, IR). Four compounds exist in the hydrazone tautomeric form. The central tin atoms in all compounds exist in slightly distorted trans-trigonal bipyramidal geometry with the 'negative' atoms (nitrogen, oxygen) in axial and the carbon atoms in equatorial positions; no intramolecular attacks from the dyes' cores were observed. The in vitro antifungal activity of the compounds studied was comparable to similar organotin(IV) compounds and antifungal drugs in clinical use. Copyright (c) 2005 John Wiley E Sons, Ltd.
eng Structure of azo dye organotin(IV) compounds containing a C,N-chelating ligand, part II, and their in vitro antifungal activity Eight complexes of azo dyes used in routine industrial processes and the [(2-dimethylaminomethyl) phenyl](R-2)tin(IV) moiety (R = Ph or n-Bu) have been prepared, their NMR, electrospray ionization mass spectrometry, IR and UV-VIS spectra measured, and the X-ray structure of ([2-(N,N-dimethylaminomethyl)phenyl](diphenyl))tin(IV)-2-{[N'-(2-oxo-1-phenylcarbamoylpropyliden)hydrazo]}benzoate (3a), determined. The compounds reveal similar structures in chloroform solution (NMR) and in the solid state (X-ray, IR). Four compounds exist in the hydrazone tautomeric form. The central tin atoms in all compounds exist in slightly distorted trans-trigonal bipyramidal geometry with the 'negative' atoms (nitrogen, oxygen) in axial and the carbon atoms in equatorial positions; no intramolecular attacks from the dyes' cores were observed. The in vitro antifungal activity of the compounds studied was comparable to similar organotin(IV) compounds and antifungal drugs in clinical use. Copyright (c) 2005 John Wiley E Sons, Ltd. organotin(IV) compounds; azo dyes; C,N-chelating ligand; NMR; X-ray diffraction; electrospray ionization mass spectrometry; azo-hydrazone tautomerism

Departments

Other Parts

Map

en.mapy.cz

Services

Popular Links

© 2023 University of Pardubice, Studentská 95, 532 10 Pardubice 2
Phone: +420 466 036 111, 466 036 112, 466 036 113
Webmaster, RSS
Data box ID: f5vj9hu
Accessibility Statement
CC BY-NC-ND 4.0Creative CommonsAttributionNonCommercialNoDerivatives