Departamento de Química Inorgánica, Universidad Autónoma de Madrid, Madrid, Spain.
J Inorg Biochem. 2011 May;105(5):600-8. doi: 10.1016/j.jinorgbio.2011.01.014. Epub 2011 Feb 3.
Several methyltin(IV) and butyltin(IV) complexes with the ligand benzil bis(benzoylhydrazone) and 4,4'-bipyridyl as coligand were synthesised and characterized by elemental analysis and by IR, (1)H, (13)C and (119)Sn NMR spectroscopies. Some of them were also analyzed using single crystal X-ray diffraction. The title compounds were evaluated for their in vitro antimicrobial properties. All buthyltin complexes showed significant inhibition of Gram positive bacteria, resulting Bacillus subtilis, Sarcina lutea and both methicillin-susceptible and methicillin-resistant Staphylococcus epidermidis the most sensitive strains. Furthermore, they were able to inhibit the growth of Gram negative bacteria, especially Proteus vulgaris, whereas no activity was exhibited against fungi. All methyltin complexes were devoid of antimicrobial properties.
几种含有配体苯甲酰基双(苯甲酰腙)和 4,4'-联吡啶作为共配体的甲基锡(IV)和丁基锡(IV)配合物被合成并通过元素分析和 IR、(1)H、(13)C 和 (119)Sn NMR 光谱进行了表征。其中一些还使用单晶 X 射线衍射进行了分析。评估了标题化合物的体外抗菌性能。所有丁基锡配合物对革兰氏阳性菌均显示出显著的抑制作用,导致枯草芽孢杆菌、藤黄微球菌以及对甲氧西林敏感和耐甲氧西林的表皮葡萄球菌成为最敏感的菌株。此外,它们还能够抑制革兰氏阴性菌的生长,尤其是普通变形杆菌,而对真菌则没有活性。所有甲基锡配合物均无抗菌性能。