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LI Ya-feng~ ** ZHANG Li-mei~ WU Lei-lei~ WANG Sheng-hai~ WANG Hai-lian~ SHANG Xuan-xuan~ . College of Chemistry Molecular Engineering . College of Mathematics Physics Qingdao University of Science & Technology Qingdao P. R. China 《高等学校化学研究》2006,(6)
IntroductionThe interest in polyoxometalates that are widelyused in medical chemistry, catalyst reactions, and ma-terial sciences stems from their complicated aggregatesformed by means of corner-, edge- and face-sha-ring[1—4]. The exploitation of new str… 相似文献
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A new complex [Ni(en)3]4[HVⅣ12VⅤ6O42(PO4)] has been hydrothermally synthesized and characterized by X-Ray diffraction, IR and Elemental analysis. Single crystal X-ray analysis indicates that this compoud crystallizes in cubic system,space group Im 3m with a=17.4081(2)?, V=5275.38(10)?3, R=0.0420, wR=0.1055, Z=2, Dc=1.663g·cm-3, μ=2.297mm-1, F(000)=2636. The crystal structure consists of [Ni(en)3]2+ cations and {HV18O42(PO4)}8- cluster anion which construct from 18 {VO5} square pyramids. The VO5 pyramids joined each other to form a {V18O42} cage hosting a tetrahedral {PO4}3- moiety with disordered oxygen atoms. CCDC: 185574. 相似文献
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以2-(2-吡啶基)咪唑(pIM)、Co2+和NaVO3为原料,在水热条件下,制备了新的钒氧簇化合物[Co (pIM) V2O6](1)。采用X射线单晶衍射、粉末X射线衍射、傅里叶变换红外光谱和元素分析等方法对化合物进行了表征。单晶解析表明,该化合物由VO4四面体和CoO3N2四方锥通过氧原子共边、共角连接成二维结构。基于钒氧簇在催化氧化体系中的高效活性,1作为非均相反应的催化剂,在以H2O2为氧化剂的催化烯烃环氧化反应中表现出优秀的催化性能,催化剂能够多次重复使用且活性基本保持不变。此外,磁化率研究表明1中存在反铁磁相互作用。 相似文献
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The synthesis and structures and thermal properties of two compounds: {(H2O)2K--(H2O)3-Co(H2O)3}2[V10O28] (1) and {(H2O)2K--(H2O)3-Ni(H2O)3}2[V10O28] (2) are described. These compounds have been prepared by the reaction of aqueous solutions (pH=3.5) of KVO3with MCl2·6H2O (M=Co, Ni) at 70–72°C. The isomorphous structures of the two compounds consist of interlinked chains composed of arrays of {V10O28} clusters which are joined through {(H2O)2K--(H2O)3-M(H2O)3} bridges. Thermogravimetric studies revealed the complete removal of all water molecules in multiple steps in the temperature range 90–208°C. 相似文献
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1 INTRODUCTION In the past years, polyoxovanadates have attracted extensive interest in solid-state material chemistry owing to the formation of mixed-valence com- pounds that exhibit rich electronic and magnetic properties relevant to catalysis, medicine and ma- terials science[1~4]. The following polyoxovanadates have been found and structurally characterized: [V5O14]3-, [V6O19]8-, [V10O28]6-, [V12O32]4-, [V13- O34]3-, [V15O36]5-, [V15O42]9-, [V17O42]4-, [V18- O42]12-, [V16O38]7… 相似文献
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以2-(2-吡啶基)咪唑(pIM)、Co2+和NaVO3为原料,在水热条件下,制备了新的钒氧簇化合物[Co(pIM)V2O6] (1)。采用X射线单晶衍射、粉末X射线衍射、傅里叶变换红外光谱和元素分析等方法对化合物进行了表征。单晶解析表明,该化合物由VO4四面体和CoO3N2四方锥通过氧原子共边、共角连接成二维结构。基于钒氧簇在催化氧化体系中的高效活性,1作为非均相反应的催化剂,在以H2O2为氧化剂的催化烯烃环氧化反应中表现出优秀的催化性能,催化剂能够多次重复使用且活性基本保持不变。此外,磁化率研究表明1中存在反铁磁相互作用。 相似文献
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Expansion of Germanato‐Polyoxovanadate Cluster Cores: Solvothermal Syntheses and Selected Properties of (trenH2)2[{M(tren)}4V15Ge6O48(H2O)] (M = Co and Zn)
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Two germanato‐polyoxovanadates with the {V15Ge6O48} cluster core are extended by covalent bonds to four transition metal amine complexes [M(tren)]2+ (M = Co and Zn, tren = tris(2‐aminoethyl)amine). The complexes have bonds to terminal atoms of the Ge2O7 units and such expansion of a germanato‐polyxovanadate was never observed before. The characterization of these compounds revealed the presence of two protonated tren molecules charge balancing the negative charges of the [{M(tren)}4V15Ge6O48(H2O)]4– anion. 相似文献
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本文采用水热技术合成了一种具有经典ACO拓扑结构的多钒氧酸盐{[Cu4(VⅣ11VⅤ7O42(PO4))(C3H10N2)8]·4H2O}n (1,C3H10N2=1,2-丙二胺),并且通过元素分析、红外、热重、单晶X-射线衍射对化合物1进行了表征。晶体学分析表明,阴离子簇[VⅣ11VⅤ7O42(PO4)]8-与8个过渡金属配合物阳离子[Cu(C3H10N2)2]2+相连而产生具有经典ACO拓扑结构的三维孔道结构。化合物1为四方晶系,P4/nnc空间群,a=b=1.505 91(10) nm,c=1.871 3(3) nm,V=4.243 8(7) nm3,Z=2。化合物1沿c轴方向具有0.753 nm×0.753 nm孔道。 相似文献
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以大环铜配合物[CuL](ClO4)2(L=5,7,7,12,14,14-六甲基-1,4,8,11-四氮杂环十四-4,11-二烯)与NH4VO3反应合成了一个新的钒氧多酸桥联大环铜配合物[CuL]2[H2V10O28]·7H2O(1),其结构经IR,元素分析和X-射线单晶衍射表征。1(CCDC: 1510831)属单斜晶系,P2(1)/n空间群,晶胞参数a=11.512(3) , b=18.170(4) , c=14.534(3) , β=102.997(4)°, V=2 962.3(11) 3, Dc=1.986 mg·cm-3, Z=2, μ=2.300 mm-1, R1=0.047 2, wR2=0.118 2。 相似文献