Synthesis, Raman, FT-IR, NMR spectroscopic data and antimicrobial activity of mixed aza-oxo-thia macrocyclic compounds
作者:Naz Mohammed Aghatabay、Yaghub Mahmiani、Hüseyin Çevik、Başaran Dulger
DOI:10.1016/j.ejmech.2008.02.038
日期:2009.1
Mixed aza-oxo-thia macrocyclic ligands 1,3,5,11,13,15-hexaaza-6,10,16,20-tetraoxo-8,18-dithia-2,3,4:12,13,14-dipyridine cyclocosane (L1); 1,3,5,12,14,16-hexeaza-6,11,17,22-tetraoxo-8,9,19,20-tetrathia-2,3,4:13,14,15-dipyridine cyclodocosane (L2); 1,3,5,13,15,17-hexaaza-6,12,18,24-tetraoxo-9,21-dithia-2,3,4:14,15,16-dipyridine cyclotetracosane (L3) and 1,3,5,14,16,18-hexaaza-6,13,19,26-tetraoxo-9,10
混合氮杂-氧-硫杂大环配体1,3,5,11,13,15-六氮杂-6,10,16,20-四氧-8,18-二硫杂-2,3,4:12,13,14-二吡啶环烷(L 1) ; 1,3,5,12,14,16-己六-6,11,17,22-四氧8,9,19,20-四硫-2,3,4:13,14,15-二吡啶环二十二烷(L 2) ; 1,3,5,13,15,17-hexaaza-6,12,18,24-tetraoxo-9,21-dithia-2,3,4:14,15,16-二吡啶环四氢烷(L 3)和1 ,3,5,14,16,18-hexaaza-6,13,19,26-tetraoxo-9,10,22,23-tetrathia-2,3,4:15,16,17-dipyrididine cyclohexacosane (L 4)进行了合成。配体的结构特征已通过元素分析拉曼,红外,1 H和13进行了研究13 C N