Synthesis, structure, cytotoxic activities, and DNA-binding of 1-D copper(II) and zinc(II) coordination polymers
被引:16
作者:
Jiang, Man
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机构:
Ocean Univ China, Marine Drug & Food Inst, Qingdao 266003, Shandong, Peoples R China
Qindao Municipal Med Grp, Qingdao 266011, Shandong, Peoples R ChinaOcean Univ China, Marine Drug & Food Inst, Qingdao 266003, Shandong, Peoples R China
Jiang, Man
[1
,2
]
Li, Yan-Tuan
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机构:
Ocean Univ China, Marine Drug & Food Inst, Qingdao 266003, Shandong, Peoples R ChinaOcean Univ China, Marine Drug & Food Inst, Qingdao 266003, Shandong, Peoples R China
Li, Yan-Tuan
[1
]
Wu, Zhi-Yong
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机构:
Ocean Univ China, Marine Drug & Food Inst, Qingdao 266003, Shandong, Peoples R ChinaOcean Univ China, Marine Drug & Food Inst, Qingdao 266003, Shandong, Peoples R China
Wu, Zhi-Yong
[1
]
机构:
[1] Ocean Univ China, Marine Drug & Food Inst, Qingdao 266003, Shandong, Peoples R China
[2] Qindao Municipal Med Grp, Qingdao 266011, Shandong, Peoples R China
Two 1-D coordination polymers have been synthesized and identified as [Zn(ox)(en)](n)(H2O)(2n) (1) and [Cu-2(dmeo)(N-3)(2)](n) (2), where en represents diaminoethane, ox and dmeo stand for dianions of oxalic acid and N,N'-bis[2-(dimethylamino)ethyl]oxamide, respectively. Polymer 1 was characterized by elemental analysis, molar conductance measurement, IR and electronic spectra, and single-crystal X-ray diffraction. Polymer 1 consists of 1-D chains bridged by oxalate. The Zn-II can be described as a distorted octahedral environment and the Zn-II center dot center dot center dot Zn-II separation through the mu-oxalato-bridge is 5.5420(9) angstrom. Hydrogen bonds assemble the coordination polymers to a 3-D supermolecular structure. The crystal structure of 2 has been reported previously. However, the bioactivities were not studied. The DNA-binding properties and cytotoxic activities of the two coordination polymers are investigated. The results suggest that the two polymers interact with HS-DNA in groove binding with binding affinity following the order of 1 > 2, which is consistent with their anticancer activities.