期刊文献+
共找到4篇文章
< 1 >
每页显示 20 50 100
一个新型的多酸基超分子化合物的合成表征及光催化和电化学传感器性能研究 被引量:1
1
作者 田爱香 金靓 应俊 《渤海大学学报(自然科学版)》 CAS 2020年第4期308-313,共6页
在水热的条件下,选择了经典的Keggin型多金属氧酸盐H_3PMo12O40与一个吡啶基五元杂环衍生物配体-2-(4-吡啶基)4,5-二(2-吡啶基)咪唑(Py3Piz)反应,通过调节pH值得到了一个新多酸基超分子化合物[(Py3Piz)PMo12O40](1)(Py3Piz=2-(4-吡啶基)... 在水热的条件下,选择了经典的Keggin型多金属氧酸盐H_3PMo12O40与一个吡啶基五元杂环衍生物配体-2-(4-吡啶基)4,5-二(2-吡啶基)咪唑(Py3Piz)反应,通过调节pH值得到了一个新多酸基超分子化合物[(Py3Piz)PMo12O40](1)(Py3Piz=2-(4-吡啶基)4,5-二(2-吡啶基)咪唑),使用红外光谱(FT-IR)与单晶X-射线衍射仪对其结构进行了表征,化合物1的结构单元包含一个游离的配体Py3Piz与一个多金属氧酸盐阴离子[PMo12O40]^3-,多酸阴离子[PMo12O40]^3-和配体Py3Piz通过氢键相互作用构成了锯齿状的1D超分子链,相邻的1D超分子链又通过氢键相互作用构成了波浪形的2D的超分子层.在性质方面研究了其光催化活性和电化学性能,结果表明化合物1对有机染料RhB具有良好的光催化降解活性,并且1-CPE对过氧化氢和亚硝酸钾具有一定的电催化性能. 展开更多
关键词 多金属氧酸盐 水热合成 电化学 光催化
下载PDF
Keggin型多金属氧酸盐与三氮唑构建的二维杂化化合物的结构与性能研究
2
作者 田爱香 于海燕 +1 位作者 关雅文 付玉帛 《渤海大学学报(自然科学版)》 CAS 2019年第2期97-102,共6页
以Keggin型多酸阴离子作为无机构筑单元,三氮唑作为有机构筑单元,于水热条件下,合成了一种二维配位化合物.该化合物分子式为C8H12Ag4Mo12N12O44V.利用元素分析、单晶X-射线衍射以及红外光谱对该多酸化合物进行了表征.该晶体属于单斜晶系... 以Keggin型多酸阴离子作为无机构筑单元,三氮唑作为有机构筑单元,于水热条件下,合成了一种二维配位化合物.该化合物分子式为C8H12Ag4Mo12N12O44V.利用元素分析、单晶X-射线衍射以及红外光谱对该多酸化合物进行了表征.该晶体属于单斜晶系,P21/n空间群.化合物的晶胞参数为a=10.665(5),A,b=20.761(9),A,c=11.518(5),A,α=90°,β=95.259°,γ=90°,V=2539.4(19)A^3,Z=4,ωR1=0.0301,ωR2=0.3036.在该化合物中,Keggin型阴离子[VMo12O40]3-和配体之间通过银离子相连,形成了化合物的1D链状结构.一维链之间通过与金属银配位,形成格子状2D层状结构. 展开更多
关键词 多金属氧酸盐 水热技术 电化学 光催化
下载PDF
Two Anderson-based supramolecular compounds modified by 4,4'-dipyridy synthesized in one-pot
3
作者 LI Tingting tian aixiang YING Jun 《分子科学学报》 CAS 2024年第2期160-166,共7页
Using symmetrical rigid organic ligand 4,4'-dipyridy(4,4'-bipy),two new Anderson-based supramolecular compounds,namely,[H_(2)(4,4'-bipy)]_(3)·(TeMo_(6)O_(24))·(H_(2)Mo_(6)O_(19))(1)and{Cu_(2)[H(4... Using symmetrical rigid organic ligand 4,4'-dipyridy(4,4'-bipy),two new Anderson-based supramolecular compounds,namely,[H_(2)(4,4'-bipy)]_(3)·(TeMo_(6)O_(24))·(H_(2)Mo_(6)O_(19))(1)and{Cu_(2)[H(4,4'-bipy)]_(2)(H_(2)O)_(6)(TeMo_(6)O_(24))}·4H_(2)O(2),were synthesized in one-pot under hydrothermal conditions.The compounds 1 and 2 have been tested by IR spectra,elemental analyses and single-crystal X-ray diffraction.Compound 1 contains one discrete Anderson anion,one Lindqvist anion and three 4,4'-bipy organic ligands.The anions and 4,4'-bipy alternate with each other by hydrogen bonding,building a supramolecular 1D chain.Adjacent 1D chains are interlinked through hydrogen bonding interactions to further connect a supramolecular 2D layer.Compounds containing both Anderson and Lindqvist polyanions are not common in the crystal structure of POMs.Compound 2 contains one Anderson anion and two metal-organic subunits{Cu_(2)[H(4,4'-bipy)]_(2)(H_(2)O)_(6)}^(6+)as modifiers.The Anderson anions and{Cu_(2)[H(4,4'-bipy)]_(2)(H_(2)O)_(6)}^(6+)subunits are organized into alternating through hydrogen bonding interactions to construct a supramolecular 1D chain.Additionally,the electrochemical properties of compounds 1 and 2 as well as photocatalytic properties are investigated.Results show that compounds 1 and 2 have photocatalytic activity,which can photocatalyze the degradation of organic dyes MB and AF.Also,compounds 1 and 2 have good electrochemical properties for amperometric detection of NO2-and Cr(Ⅵ).Furthermore,Compound 2 can be used as materials of supercapacitor. 展开更多
关键词 Anderson POM hydrothermal syntheses supramolecular structure ELECTROCHEMISTRY PHOTOCATALYSIS
原文传递
Substituent groups from aromatic dicarboxylates modulated structural diversification in the assembly of Co(Ⅱ)complexes based on the bis-pyridyl-bis-amide ligands 被引量:2
4
作者 WANG XiuLi MU Bao +4 位作者 LIN HongYan YANG Song LIU GuoCheng tian aixiang ZHANG JuWen 《Science China Chemistry》 SCIE EI CAS 2013年第5期557-566,共10页
Four coordination polymers based on two bis-pyridyl-bis-amide ligands and three aromatic dicarboxylates with different substituent groups, namely, [Co(3-bpcb)x.5(NPH)(H20)]" 4H20 (1), [Co(3-bpcb)(NIPH)] ... Four coordination polymers based on two bis-pyridyl-bis-amide ligands and three aromatic dicarboxylates with different substituent groups, namely, [Co(3-bpcb)x.5(NPH)(H20)]" 4H20 (1), [Co(3-bpcb)(NIPH)] (2), [Co(3-bpcb)0.5(5-H2AIP)]" 2H20 (3), [Co(3-bpcd)0.5(5-H2AIP)(H20)]" 2H20 (4) [3-bpcb = N,N'-bis(3-pyridinecarboxamide)-l,4-benzene, 3-bpcd = N,N'-bis(3- pyridine)cyclohexane-l,4-dicarboxamide, H2NPH = 3-nitrophthalic acid, H2NIPH = 5-nitroisophthalic acid, 5-HaAIP = 5-aminoisophthalic acid] have been synthetized under hydrothermal conditions. Complex 1 displays a one dimensional (1D) chain based on the binuclear [Co2(NPH)2] units and 3-bpeb ligands, which is extended into a three dimensional (3D) supra- molecular framework through hydrogen bonding and n-n stacking interactions. In complex 2, the (3,5)-connected two dimen- sional (2D) layers are constructed from 1D Co-NIPH chains and bidentate-bridging 3-bpeb ligands. Complex 3 is a 2D double layer based on Co-5-H2AIP 2D layers and 3-bpeb pillars. Complex 4 also displays a 2D network, which is constructed from the Co-5-H2AIP 1D double chains and 3-bpcd ligands. Finally, complexes 2--4 are extended into 3D supramolecular frame- works by hydrogen bonding or n-re stacking interactions. The substituent groups of dicarboxylates play an important role in the assembly and structures of the title complexes. In addition, the fluorescent properties of complexes 1-4 and the electrochemi- cal behaviors of 3 and 4 at room temperature have been investigated. 展开更多
关键词 coordination polymer bis-pyridyl-bis-amide ligand hydrothermal reaction fluorescent property
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部