摘要
采用3,5-二(4-吡啶)1,2,4-三唑(Hbpt)为配体与钴盐反应,在水热法条件下成功合成了3个配合物,分别是:[Co(Hbpt)2(HCOO)2(H2O)2]n·4nH2O(1),[Co(Hbpt)2(HCOO)2(H2O)2]n(2)和[Co(bpt)2(H2O)4]n·2nH2O(3),并通过X-射线单晶衍射和红外对它们进行了表征。配合物1和2均为三斜晶系,P1空间群,配合物3为单斜晶系,P21/c空间群。中心金属Co(Ⅱ)都是六配位,每个Co(Ⅱ)分别与2个Hbpt配体桥联而形成零维的结构单元,这些结构单元通过氢键和π-π堆积弱作用进一步连接而形成三维超分子网络结构。此外,还对配合物1和3的热稳定性做了分析。
Three Co (Ⅱ) complexes constructed from 3,5-bis(4-pyridyl)-1,2,4-triazolyl(Hbpt), namely [Co(Hbpt)2(HCOO)2(H2O)2]n·4n H2O(1), [Co(Hbpt)2(HCOO)2(H2O)2]n(2) and [Co(bpt)2(H2O)4]n·2n H2O(3), have been hydrothermally synthesized and structurally characterized by IR spectroscopy and single crystal X-ray diffraction.The X-ray crystallographic analyses show that all of them present three-dimensional supramolecular frameworks in which crystal configurations are linked by π-π stacking interactions and strong intermolecular hydrogenbonding interactions. In addition, the thermogravimetric analyses(TGA) for complexes 1 and 3 are also discussed.CCDC: 1001364, 1; 1001365, 2; 1001366, 3.
出处
《无机化学学报》
SCIE
CAS
CSCD
北大核心
2014年第11期2645-2652,共8页
Chinese Journal of Inorganic Chemistry
基金
浙江省自然科学基金(No.LY12B01002)
浙江师范大学“浙江省省属高校化学重中之重学科”和“先进催化材料教育部重点实验室”开放课题基金项目资助