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The crystal and molecular structures of [(C3H7O)2PS2]2 (CCDC No.217201) were determined by means of X-ray crystallography. It crystallized in a triclinic system with space group P-1 and lattice parameters a=0.82794(3) nm, b=0.84764(2) nm, c=0.85034(3) nm, α=97.78(3)°, β=110.77(3)°, γ= 94. 95 (3)°,V= 0. 54701(9) nm3, Z= 1. In this molecule, the two diisopropyl dithiophosphate groups, [(C3H7O)2PS2]2,which are parallel to each other, are linked by an S-S bond and there exist inversion centers in the molecule.In the structure, the P=S bonds in the two dithiophosphate units are trans-oriented to each other. 相似文献
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MAO Hong-yan LIU Hong-lei ZHANG Hong-yun XU Chen WANG En-bo HAN Hua-yun WU Qing-an ZHU Yu 《高等学校化学研究》2004,20(3):277-280
The combination of both 4,4′-bipyridine(4,4′-bipy) and dihydrogen phosphate anion ligands with copper(Ⅱ) results in the formation of a novel layered compound Cu(4,4′-bipy)2(H2PO4)2(H2O)2. The crystal structure comprises discrete neutral Cu(4,4′-bipy)2(H2PO4)2(H2O)2 units. The copper atom, located on the crystallographic twofold axis, is coordinated with two nitrogen atoms of terminal 4,4′-bipy ligands and two water molecules at the equatorial positions, and two dihydrogen phosphate oxygen atoms at the axial positions, forming an elongated octahedron. The complex is a two-dimensional distorted rhomboidal network possessing two kinds of rhomboids with dimensions of ca. 1.6792 nm×0.3203 nm and 1.2778 nm×0.3198 nm, respectively. The two-dimensional networks are stacked parallelly on each other along c-axis to give an extended three-dimensional channel network with an interlayer distance of ca. 0.5030 nm. Crystal data: triclinic, space group P1, a=1.0253(2) nm, b=1.4501(3) nm, c=0.79715(16) nm, α=97.91(3)°, β=90.99(3)°, γ=85.54(3)°, V=1.1703(4) nm3, Z=2, R=0.0892, wR=0.2451. 相似文献
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A novel dimer-tungstovanadate,(H3O)4[VW12O40Na(H2O)4]2,was hydrothermally synthesized and structurally characterized by single crystal X-ray diffraction,IR spectra,TGA-DSC thermal analysis and polarograpy.The yellowish crystal crystallized in the triclinic system,space group ,a=1.464 5(3) nm,b=1.4686(3) nm,c=1.4111(3) nm,α=111.82(2)°,βA novel dimer-tungstovanadate,(H3O)4[VW12O40Na(H2O)4]2,was hydrothermally synthesized and structurally characterized by single crystal X-ray diffraction,IR spectra,TGA-DSC thermal analysis and polarograpy.The yellowish crystal crystallized in the triclinic system,space group ,a=1.464 5(3) nm,b=1.4686(3) nm,c=1.4111(3) nm,α=111.82(2)°,β=93.17(3)°,γ=117.47(3)°,V=2.2106(8) nm3,Z=1,Dc=4.552 g.cm-3,λ(Mo Kα)=0.071073 nm,μ=31.402 mm-1,F(000)=2648,R=0.0780.The title compound consists of two Keggin structure units linked together with two hydrated sodium cations to form a dimer with a porous structure with the pore dimension of 0.766 nm×0.7785 nm. 相似文献
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Chiralityduetoalkylbranchingisabundantamongseveralnaturallyoccurringsecondarymetabolites .Thisstructurefeatureisparticularlypredominantamonginsectpheromones[1] ,manyofwhichareofeconomicsignificance .Asaresult,aconsiderableefforthasbeenmadetosynthesizethem… 相似文献
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镧系四元混配化合物[Ln(BA)2(NO3)(phen)]2的合成、晶体结构和波谱研究 总被引:3,自引:0,他引:3
在酸性介质、含水溶剂中合成了四元混配化合物[Ln(BA)2(NO3)(phen)]2(BA=苯甲酸根;Ln=La,Ce,Pr,Nd,Sm,Eu,Dy,Gd,Tb,Er),用元素分析、IR、DTA-TG等方法对配合物进行了表征.研究了配合物的顺磁性能和荧光性能.镨配合物的单晶衍射结果表明,配合物属三斜晶系,双核,Pr3+的配位数为9,4个BA呈二种配位方式,丰富了四元配合物的结构表现形式. 相似文献
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A new tetradecaborate, [H3N(CH2)2NH3]2[B14O20(OH)6](1), was synthesized by a boric acid ‘flux’ method, and characterized by X-ray powder diffraction, ICP, IR, TGA and DTA analyses. Single-crystal X-ray diffraction analysis showed that it crystallized in the monoclinic space group P1(No.2) with a=0.85092(10) nm, b=0.88678(11) nm, c=1.00724(13) nm, α=95.099(2)o, β=96.950(2)o, γ=116.845(2)o, V=0.66425(14) nm3, Z=2, R1=0.0625[I2σ(I)], and wR2=0.1172(all data). The molecule structure of compound 1 comprises the isolated polyanion clusters [B14O20(OH)6]4– and diprotonated ethylenediamine molecules. Each polyanion cluster contains an 8-ring enclosed by six B3O3 3-ring units. Adjacent clusters are further connected with each other through strong hydrogen-bonding interactions of N(O)―H···O to form a three dimensional(3D) supramolecular structure with 2D pseudo channels along the [010] and [001] directions. The diprotonated ethylenediamine molecules located in the channels interact with the host through extensive hydrogen-bonds. Compound 1 presents few example containing isolated polyborate anions synthesized by a boric acid ‘flux’ method. 相似文献
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Two new layered lanthanide sulfates,[C10H10N2][Pr2(SO4)4(H2O)2](1)and[H5O2][Sm(SO4)2(H2O)3](2)were synthesized via solvothermal reaction and structurally characterized by single-crystal X-ray diffraction(XRD), infrared(IR) spectroscopy, thermal analysis, fluorescent spectra and inductively coupled plasma(ICP). Crystal data for compound 1, triclinic, P space group, a=0.8052(4) nm, b=0.9438(4) nm, c=1.4990(7) nm, α=79.450(5)°, β= 83.703(5)°, γ=74.048(5)°, V=1.0746(9) nm3, Z=2; for compound 2, monoclinic, P21/c space group, a=0.6599(11) nm, b=1.8940(3) nm, c=0.8765(14) nm, β=96.596(2)°, V=1.0883(3) nm3, Z=4. Structure analysis indicates that both the compounds exhibit a 2D corrugated layer structure, with protonated 4,4'-bipyridine cations and water dimmers (H5O2)+ located between the inorganic layers of compounds 1 and 2, respectively. Luminescent properties of compounds 1 and 2 were further investigated. 相似文献
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Katsuyuki Aoki 《高等学校化学研究》2005,21(4):396-400
Fe(Ⅱ) complex Fe[HB(pz)3]2(compound 1, pz=pyrazole) and Ni(Ⅱ) complex Ni[HB(pz)3]2(compound 2) have been obtained by the reaction of MCI2(M=Fe and Ni) with NaHB(pz)3 in MeOH. The two complexes(compounds 1 and 2) were characterized by IR, NMR, elemental analysis and X-ray diffraction. Compound 1 crystallizes in space group P21/c with a=1.224(3) nm, b=1.161(2) nm, c=1.648(3) nm, β=107.62(15)°, V=2.233(8) nm3, Z=2. Compound 2 crystallizes in space group P21/c with a=0.97926(18) nm, b=1.7423(3) nm, c=1.3156(2) nm, β=97.055(16)°, V=2.2277(7) nm3, Z=4. The results of X-ray structural analyses show that both compounds 1 and 2 are monomeric neutral, possessing a similar coordination mode and a similar structure around the metal centers. The related spectral characterizations, steric effects and binding properties are discussed. 相似文献
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采用Gly-Glyo,2,2'-联吡啶与Cu(NO3)2·H2O在二次水溶液中反应,合成了以Gly-Glyo作为中继基的新型双核配合物.经X射线单晶结构分析确定该配合物晶体的化学结构式[(C10H8N2)Cu(H2NCH2CONHCH2COO)Cu(C10H8N2)2](NO3)3.晶体属三斜晶系,P1空间群,晶胞参数:a=1.4268nm,b=1.1754nm,c=1.4059nm,α=104.01°,β=91.56°,γ=72.22°,Z=2.衍射数据在NicoletXRDR3型四圆衍射仪上收集,结构参数经块矩阵最小二乘法精修后,最终一致性因子R值为0.070. 相似文献
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ZHANG Hong LI Yang guang LAN Yang WANG Xiu liDuan Li ying WANG En bo ** HU Chang wenInstitute of Polyoxometalate Chemistry Department of Chemistry Northeast Normal University Changchun P. R. ChinaYAO Yuan gen CHEN Jiu tong 《高等学校化学研究》2002,18(3):252-254
IntroductionLayered intercalation compounds haveattracted increasing research attention due to theirapplications in diverse areas,for instance,some ofthem are used as rechargeable batteries,heterogeneous catalysts,and an exchange[1— 12 ] . Inprevious literatures,several layered mixed- valencevanadium oxides were reported,such as VO2 · 1 /2 H2 O[13 ] ,[H2 N( CH2 ) 4 NH2 ]V4O9[14 ] ,NH4V3 O8[15] ,( C6H14 · N2 ) V6O14 · 1 / 2 H2 O[16] ,[HN( C2 H4) 3 NH]V6O14 [17] ,NMe4V6O14 [18]… 相似文献