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首页> 外文期刊>Inorganica Chimica Acta >Syntheses, structures and properties of three Keggin-based metal-organic complexes derived from flexible bis-pyridyl-bis-amide and rigid phenanthroline mixed ligands
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Syntheses, structures and properties of three Keggin-based metal-organic complexes derived from flexible bis-pyridyl-bis-amide and rigid phenanthroline mixed ligands

机译:源自柔性双吡啶基双酰胺和刚性菲咯啉混合配体的三种Keggin基金属有机配合物的合成,结构和性质

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摘要

Three Keggin-type polyoxometalate (POM)-based metal-organic complexes (MOCs) constructed from mixed ligands of phenanthroline (phen) and flexible bis-pyridyl-bis-amide ligands with different spacer length: [Cu_2(SiW_(12)O_(40))L~1(phen)_2(H_2O)]·3H_2O (1), [Cu_2(SiW_(12)O_(40))L~2(phen)_2(H_2O)4] (2) and [Cu_2(SiW_(12)O_(40))L~3(phen)_2(H_2O)_4]·6H_2O (3) (L~1 = N,N0-bis(3-pyridinecarboxamide)-1,2-ethane, L~2 = N, N0-bis(3-pyridinecarboxamide)-1,4-butane, L~3 = N,N0-bis(3-pyridinecarboxamide)-1,6-hexane), have been synthesized under hydrothermal conditions and structurally characterized by single crystal X-ray diffraction analyses, elemental analyses, thermogravimetric (TG) analyses, IR spectra and powder X-ray diffraction (PXRD) analyses. Complex 1 exhibits a 2D network, in which [SiW12O_40]4~- (SiW12) anions act as tetradentate linkages. Complex 2 is a 0D structure containing a dinuclear complex cation [Cu_2L~2(- phen)_2(H_2O)_4]~(4+) and a discrete SiW12 anion. Complex 3 shows a 1D chain structure, in which the SiW12 anions as bidentate linkages bridge the adjacent complex cations [Cu_2L~3(phen)_2(H_2O)_4]~(4+). The spacer lengths of the bis-pyridyl-bis-amide ligands play important roles in tuning the structures of the title complexes. In addition, the introduction of the secondary ligand phen shows significant effect on the dimensionalities of POM-based bis-pyridyl-bis-amide complexes. The electrochemical behavior and electrocatalytic properties of complex 3, as well as the photocatalytic activities of the title complexes have been studied.
机译:由菲咯啉(phen)和具有不同间隔长度的柔性双吡啶基-双酰胺配体的混合配体构建的三种基于Keggin型多金属氧酸盐(POM)的金属-有机配合物(MOC):[Cu_2(SiW_(12)O_( 40))L〜1(phen)_2(H_2O)]·3H_2O(1),[Cu_2(SiW_(12)O_(40))L〜2(phen)_2(H_2O)4](2)和[Cu_2 (SiW_(12)O_(40))L〜3(phen)_2(H_2O)_4]·6H_2O(3)(L〜1 = N,N0-双(3-吡啶甲酰胺)-1,2-乙烷,L 〜2 = N,N0-双(3-吡啶甲酰胺)-1,4-丁烷,L〜3 = N,N0-双(3-吡啶甲酰胺)-1,6-己烷),已在水热条件下合成,结构通过单晶X射线衍射分析,元素分析,热重(TG)分析,IR光谱和粉末X射线衍射(PXRD)分析进行表征。配合物1具有2D网络,其中[SiW12O_40] 4-(SiW12)阴离子充当四齿键。络合物2为0D结构,其包含双核络合物阳离子[Cu_2L〜2(-phen)_2(H_2O)_4]〜(4+)和离散的SiW12阴离子。配合物3显示一维链结构,其中SiW12阴离子作为双齿键桥接相邻的配合物阳离子[Cu_2L〜3(phen)_2(H_2O)_4]〜(4+)。双-吡啶基-双-酰胺配体的间隔长度在调节标题复合物的结构中起重要作用。另外,第二配体phen的引入对基于POM的双-吡啶基-双酰胺复合物的尺寸显示出显着影响。研究了配合物3的电化学行为和电催化性能,以及标题配合物的光催化活性。

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