作者: Yan An , Yan-Yong Lin , Hui Wang , Hong-Zhe Sun , Ming-Liang Tong
DOI: 10.1039/B616754C
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摘要: Two highly charged zinc complexes, [Zn(L1)3](ClO4)8·4H2O (1) and [Zn(L2)2Br](ClO4)5·H2O (2) (L1 = 5,5′-di(1-(triethylammonio)methyl)-2,2′-dipyridyl L2 5,5′-di(1-(tributylammonio)methyl)-2,2′-dipyridyl) were synthesized structurally characterized by crystallography. The atom in 1 shows a distorted octahedral sphere. Variable-pH NMR studies on demonstrated that the saturated six-coordinated [Zn(L1)3]8+ species can partially change into five-coordinated [Zn(L1)2(H2O)]6+ aqueous solution. 2 trigonal-bipyramidal average distance of coordinated Br to cationic N is ca 5.9 A, which comparable adjacent phosphodiesters DNA (ca. 6 A). Both complexes exhibited high nuclease activitiestowards cleavage supercoiled plasmid with activity being maximum under physiological pH. effective may be attributed strong electrostatic interaction metal moiety two positive pendants phosphodiester groups nucleic acid.