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Synthesis,characterization and antibacterial activity of 3‐(2‐methoxyphenyl)‐2‐sulfanylpropenoic acid and di‐isopropylammonium [3‐(2‐methoxyphenyl)‐2‐sulfanylpropenoato] triphenylstannate(IV). The crystal structure of [HQ][SnPh3(o‐mpspa)]
Authors:Pedro Álvarez‐Boo  José S Casas  Eduardo E Castellano  M Delfina Couce  Rosa Farto  Eduardo Freijanes  José Sordo
Institution:1. Departamento de Química Inorgánica, Universidade de Vigo, E‐36310 Vigo, Spain;2. Departamento de Química Inorgánica, Universidade de Santiago de Compostela, E‐15782 Santiago de Compostela, Spain;3. Instituto de Física de S?o Carlos, Universidade de S?o Paulo, S?o Carlos, SP, Brazil;4. Laboratorio de Microbiología, Universidade de Vigo, E‐36310 Vigo, Spain
Abstract:Reaction of 3‐(2‐methoxyphenyl)‐2‐sulfanylpropenoic acid H2(o‐mpspa)] with SnPh3OH in the presence of di‐isopropylamine resulted in the formation of the complex HQ]SnPh3(o‐mpspa)] (where HQ = di‐isopropylammonium cation and o‐mpspa = 3‐(2‐methoxyphenyl)‐2‐sulfanylpropenoato), which was characterized by mass spectrometry and vibrational spectroscopy, as well as by 1H, 13C and 119Sn NMR spectroscopy. The single‐crystal X‐ray structural analysis of the new complex shows a trigonal‐bipyramidal coordination geometry around the Sn atom where o‐mpspa behaves as a bidentate chelating ligand. Dimeric units arise from the existence of N? H…O hydrogen bonds between the NH2 group of the di‐isopropylammonium cation and the oxygen atoms of the two neighbouring carboxylato groups. The bacteriostatic activity of the complex is also reported. Copyright © 2007 John Wiley & Sons, Ltd.
Keywords:tin  triphenyltin complexes  3‐(2‐aryl)‐2‐sulfanylpropenoic acids  X‐ray  antibacterial activity
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