摘要
Sulfate-centered Preyssler-type polyoxometalate was used as the precursor to react with transition metal cations and organic ligand for constructing inorganic-organic hybrid materials {H[Ni2（H2O）4（Htrz）3]2（KSsW30O110）}·18H2O （trz = 1,2,4-triazole） （1）, which was characterized by single crystal X-ray diffraction analysis, energy-dispersive X-ray （EDX）, power X-ray diffraction （PXRD）, IR spectra and thermogravimetric （TG） analyses. In 1, the cylindrical vacancy of the inorganic crown-type anion （SsW30Ouo） captures a K^＋ ion resulting in the anion {KS5W3oO110）^9-, which was further connected by dimeric [Ni2（H2O）4（Htrz）3]2 metal-organic units into an one-dimensional （1D） chain-like structure. These 1D chains are further packed to form a three-dimensional （3D） supramolecular structure via Hbonding interactions. Here, the sulfate-centered Preyssler-typepolyoxometalate was firstly used to coordinate with transition metal cations and introduced into the inorganic-organic hybrid materials. Electrocatalytic study indicates that compound I exhibits good electrocatalytic activity toward reduction of H2O2 and NO2^-.
Sulfate-centered Preyssler-type polyoxometalate was used as the precursor to react with transition metal cations and organic ligand for constructing inorganic-organic hybrid materials {H[Ni2（H2O）4（Htrz）3]2（KSsW30O110）}·18H2O （trz = 1,2,4-triazole） （1）, which was characterized by single crystal X-ray diffraction analysis, energy-dispersive X-ray （EDX）, power X-ray diffraction （PXRD）, IR spectra and thermogravimetric （TG） analyses. In 1, the cylindrical vacancy of the inorganic crown-type anion （SsW30Ouo） captures a K^＋ ion resulting in the anion {KS5W3oO110）^9-, which was further connected by dimeric [Ni2（H2O）4（Htrz）3]2 metal-organic units into an one-dimensional （1D） chain-like structure. These 1D chains are further packed to form a three-dimensional （3D） supramolecular structure via Hbonding interactions. Here, the sulfate-centered Preyssler-typepolyoxometalate was firstly used to coordinate with transition metal cations and introduced into the inorganic-organic hybrid materials. Electrocatalytic study indicates that compound I exhibits good electrocatalytic activity toward reduction of H2O2 and NO2^-.
基金
supported by the National Natural Science Foundation of China(No.21671032)
Science and Technology Development Project Foundation of Jilin Province(No.20150520001JH)
Science and Technology Research Foundation of the Thirteenth Five Years of Jilin Educational Committee(No.[2015]0056/JJKH20170605KJ)
