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A Cu(Ⅱ) complex [Cu(L)1.5(OSO3)]·3H2O (1) [L=1,4-bis(imidazol-1-yl)benzene] was synthesized by reaction of ligand L with CuSO4·5H2O using solvothermal method and its structure was determined by X-ray crystal structure analysis. The structure indicates that the complex crystallizes in triclinic, space group P1 with a=0.948 8(2), b=1.078 5(2), c=1.108 4(2) nm, α=74.820(2), β=81.331(2), γ=72.638(2)°, V=1.041 5(3) nm3, Z=2, Dcalc=1.687 g·cm-3, F(000)=544, μ=1.205 cm-1, the final R=0.062 3 and wR=0.132 8. The Cu(Ⅱ) atom has distorted square-pyramidal environment with a N3O2 donor set. Each L ligand links two Cu(Ⅱ) atoms using its imidazole groups to form an infinite one-dimensional (1D) ladder-like chain, which further linked by SO42- to form a two-dimensional (2D) network structure. The 2D sheets are further connected by C-H…O hydrogen bonds to give a three-dimensional (3D) structure. CCDC: 650388. 相似文献
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以5-[N-乙酸根(4-吡啶基)]四唑为桥联配体,分别与Cu(ClO)2·6H2O和CdCl2的水溶液反应,获得配聚物[Cu(a4-ptz)2·2H2O]n (1)和[{Cd(a4-ptz)·(H2O)2Cl}·H2O]n (2),2个化合物通过元素分析、IR、TGA等表征,并测定了它的晶体结构。结果表明:化合物1是一个二维四方格子结构的配位聚合体,化合物2含有四元环(Cd2Cl2)的一维Z-型聚合链。化合物2在280 ℃以下热稳定性好,并且不溶于一般溶剂,因此可成为潜在的荧光材料。 相似文献
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铁酸钴纳米微粒的共沉淀法制备和磁性质(英) 总被引:5,自引:0,他引:5
The cobalt ferrite nanoparticles were prepared by coprecipitation in the presence of poly (N-vinylpyrrolidone) (PVP) and characterized by XRD, TEM, EDX and magnetometry. XRD results suggest the formation of pure cobalt ferrite. The mean particle sizes of CoFe2O4 samples annealed at 400 ℃ and 600 ℃ were ca. 6 and 25 nm, respectively as obtained by transmission electron microscopy (TEM). The magnetic measurements indicated that nano-particles obtained at 400 ℃ were superparamagnetic while that prepared at 600 ℃ were ferrimagnetic. 相似文献
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合成了3种离子对配合物 [1-benzyl-3-bromopyridium]+[Ni(mnt)2]- (1),[1-(4′-flurobenzyl)-3-bromopyridiunm]+[Ni(mnt)2]- (2),[1-(4′-cholorobenzyl)-3-bromopyridium]+[Ni(mnt)2]- (3),(mnt=马来二腈基二硫烯,maleonitrile dithiolate)获得了单晶并解析了它们的单晶结构。 相似文献
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合成了通过N-N键桥联的不对称的N2O3席夫碱配体(H3L)的镍(Ⅱ)配合物[Ni2(HL)2]2(DMF)8(H2O)2 (1)。配合物晶体属于三斜晶系,空间群为P1,a=1.273 5(2) nm,b=1.360 4(3) nm,c=1.427 6(3) nm,α=85.358(4)°,β=63.513(3)°,γ=79.545(4)°,V=2.176 8(7) nm3,Z=1,F(000)=980,R1=0.073 6。配合物1的不对称单元中含有两个双核结构Ni2(HL)2(DMF)2(H2O)2 (Ⅰ)和Ni2(HL)2(DMF)4 (Ⅱ)以及两个DMF溶剂分子。通过酚基氧原子桥联的镍-镍距离分别为:Ni(1)-Ni(1A),0.308 4 nm;Ni(2)-Ni(2B),0.310 3 nm(对称操作:A:1-x,2-y,-z;B:1-x,1-y,1-z)。金属镍(Ⅱ)离子采取扭曲的八面体配位构型,一个配体的NO2三齿配位单元和另一个配体的酚基氧原子位于赤道面位置,两个溶剂分子占据轴向位置。晶体中存在着分子内以及分子与溶剂分子间的两种氢键作用。配合物1的变温磁化率测定表明,Ni(Ⅱ)离子之间的反铁磁耦合作用在它的磁性质中起主导作用。 相似文献
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Shibasaki小组设计合成了一系列既含有Lewis酸又含有Bronsted碱的双活性中心催化剂,并应用于一系列不对称反应中,取得了巨大的成功.受双活性中心的启发,我们认为选用在同一催化剂分子中,引入两种Lewis酸性不同的软、硬Lewis酸,两种金属就有可能分别导引参加反应的亲电试剂以及亲核试剂,从而既能大幅度地提高反应的选择性,又能提高催化反应的活性及催化剂的效率,我们称之为"软硬Lewis酸协同效应".我们合成了以手性Salen(t-Bu)为配体的镓钛双金属有机化合物,并以此为催化剂催化苯硫酚对环氧化合物的不对称开环反应,反应效果比Salen(t-Bu)镓或钛单核金属有机化合物都有明显的提高. 相似文献
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5-amino-l,10-phenanthroline (5-AP), as a tautomeric heterocyclic aromatic chelating fluorophore (THACF), can sense Zn^2+ selectively by shifting emission from 495 to 564 nm upon Zn^2+ addition in ethanol. The ratiometric fluorescent sensing behavior has been correlated to the tautomerization of 5-AP affected by solvents and metal chelation. The strategy using THACF as ratiometric fluorescent sensor for Zn^2+ not only simplifies the synthetic procedure but also gives a promising alternative for Zn^2+ ratiometric fluorescent sensor design. 相似文献
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采用水热法合成了一种新的三维配位聚合物[Zn6(bta)4(2,2′-bipy)3](H3bta=1,3,5-苯三乙酸;2,2′-bipy=2,2′-二联吡啶),并通过X射线单晶结构分析、红外光谱、元素分析和热重分析对该配合物进行了表征.结构分析数据表明,该配合物属单斜晶系,Cc空间群,晶胞参数a=1·7714(4)nm,b=2·4391(5)nm,c=1·7120(3)nm,β=104·39(3)°,Z=4,V=7·165(2)nm3,Dc=1·722g/cm3,μ=2·065mm-1,F(000)=3768,R1=0·0645,wR2=0·1424.荧光光谱结果表明,配合物具有良好的荧光性质. 相似文献
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