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1.
同多化合物[C6H5CH2NH(CH3)2]4[Mo8O26]·4H2O的合成与晶体结构 总被引:2,自引:2,他引:0
以MoO3和C6H5CH2N(CH3)2为原料,制得[C6H5CH2NH(CH3)2]4[Mo8O26]·4H2O,并通过扩散法得到无色透明晶体.X射线单晶衍射表明,晶体属三斜晶系,空间群为P墿,晶胞参数a=1.0685(2)nm,b=1.4050(3)nm,c=1.0643(2)nm,α=93.12(3)°,β=110.26(3)°,γ=71.41(3)°,V=1.4179(5)nm3,R=0.0383. 相似文献
2.
《European Journal of Solid State and Inorganic Chemistry #》1998,35(10-11):629-637
After a short survey of what is the present state of the cyclophosphates associated with the organic molecule NH2(CH2)4NH2, we report chemical preparation and crystal structure for a new example of such compounds. [NH3(CH2)4NH3]2P4O12.2H2O is monoclinic (S.G. : P21/n), with Z = 2 and the following unit-cell parameters : a = 7.6728(8) Å, b = 18.962(3) Å, c = 7.9789(9) Å β = 111.751(9)°. Bidimensional layer arrangement of P4O12 rings connected to the water molecules thanks to weak H-bonds run parallel to the ab plane. The organic groupements located between these inorganic planes perform the three-dimensional cohesion by NH····O hydrogen bonds. 相似文献
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《Solid State Sciences》2004,6(2):229-233
Two new organically templated zinc selenites MIL-86 or [H2N(CH2)2NH2]2·Zn4(SeO3)4 and MIL-87 or [H3N(CH2)3NH3]4·Zn4(SeO3)8 have been prepared by the reaction of ZnO with SeO2 under hydrothermal conditions in the presence of organic amines. Crystal data: MIL-86, monoclinic, space group P21/n, a=6.7712(4) Å, b=9.4520(5) Å, c=8.0295(4) Å, β=113.601(1)°, V=470.91(4) Å3; MIL-87, orthorhombic, space group Pbcm, a=8.8311(3) Å, b=7.8391(2) Å, c=16.2992(4) Å, V=1128.36(6) Å3. MIL-86 combines the structural features of templated networks and coordination polymers. Its structure is built up from ZnO3N tetrahedra and SeO3 pseudo-pyramids as the polyhedral building units. The ZnN bond corresponds to a direct link between zinc and the ethylenediamine template. In the other hand, MIL-87 is built up from chains of vertex-linked ZnO4 and SeO3 building units crosslinked by 1,3-diammonium propane cations. These structures are understood by comparison with the already known organically templated zinc phosphites. 相似文献
5.
Berislav Perić Nevenka Brničević Marijana Jurić Pavica Planinić Dubravka Matković-Čalogović 《Structural chemistry》2009,20(5):933-941
Abstract The compound [NH4][(CH3)2NH2]2[Ta(C2O4)4]·2H2O has been synthesized and characterized by elemental and TG/DTA analyses, IR spectroscopy and by the single-crystal X-ray
diffraction study. The structure comprises the [Ta(C2O4)4]3− anion, NH4
+ and [(CH3)2NH2]+ cations and crystallization water molecules. The Ta atom is octacoordinated by oxygen atoms from four bidentate oxalate groups
forming a coordination polyhedron close to the triangular dodecahedron. The charge-assisted hydrogen bonds from both cations
connect the [Ta(C2O4)4]3− anions into a three-dimensional framework.
Graphical Abstract The synthesis and properties of [NH4][(CH3)2NH2]2[Ta(C2O4)4]·2H2O, the first structurally characterized compound with the tetra(oxalato)tantalate(V) anion, is reported.
相似文献
6.
Gladysheva M. V. Plyusnin P. E. Komarov V. Yu. Tsygankova A. R. Gerasimov E. Yu. Shubin Yu. V. Korenev S. V. 《Journal of Structural Chemistry》2022,63(4):556-568
Journal of Structural Chemistry - New complex salts [Pd(NH3)4][Pd(NH3)3NO2][CrOx3]·H2O I, [Pd(NH3)4][Pd(NH3)3NO2][CoOx3]·H2O II, and a series of solid solutions... 相似文献
7.
利用水热法首次合成了具有两种配位环境Cd原子的新型杂多蓝化合物[NH3(CH2)2NH3]5[Cd(H2O)][CdMoV12O30(HPO4)6(H2PO4)2]·5H2O.通过元素分析、ICP、TG和X射线单晶衍射确定了其组成,使用IR和EPR进行了结构表征.通过N2吸附脱附测定了比表面积和孔径,为催化研究提供了基础数据.结果表明:该晶体为三斜晶系,P-1空间群;晶胞参数a=1.200 2(2)nm,b=1.465 1(3)nm,c=2.119 2(4)nm,V=3.5642(12)nm3,β=83.01(3)°,Z=2,F(000)=293 2,R1=0.0300,wR3=0.071 6. 相似文献
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(C5H4CH3)3Ho和(C5H4CH3)2Ho(C5H5)与5-本基四唑在THF中反应,得到了复合产物「(C5H4CH3)2HoN4CPh」2.「(C5H4CH3)(C5H5)HoN4CPh」2,该晶体属三斜晶系,P1空间群,晶胞参数为a=9.386(3),b=13.071(3),c=16.571(2)A,α=86.90(1),β=74.61(2),γ=77.30(2)°,V=1912.8(8 相似文献
10.
无机-有机杂化钒氧酸盐由于其结构的多样性以及在催化、医药、光、电、磁等材料领域中的应用前景而受到人们的广泛关注。近年来这一研究领域的重大进步是将有机氮配体或者过渡金属配合物直接连接到矾氧骨架上以获得各种新奇结构。合成出许多属于L/V/O、MXLY/V/O、L/P/V/O和MXLY 相似文献
11.
X. F. Wang X. Zh. Liu J. Wang Zh. H. Zhang W. Sun Y. M. Kong X. D. Zhang 《Russian Journal of Coordination Chemistry》2008,34(2):134-145
The three title complexes, NH4[HoIII(Edta)(H2O)3] · 1.5H2O (I) (H4Edta = ethylenedianine-N,N,N′,N′-tetraacetic acid), (NH4)4[Ho 2 III (Dtpa)2] · 9H2O (II) (H5Dtpa = diethylenetriamine-N,N,N′,N″,N″-entaacetic acid), and (NH4)3[HoIII(Ttha)] · 5H2O (III) (H6 Ttha = triethylenetetramine-N,N,N′,N″,N?,N?-hexaacetic acid), have been prepared and characterized by FT-IR, elemental analyses, and single-crystal X-ray diffraction technique. Complex I has a nine-coordinate mononuclear structure with distorted monocapped square antiprismatic conformation and its crystal structure belongs to orthorhombic system and Fdd2 space group. The crystal data are as follows: a = 19.343(9), b = 35.125(17), c = 12.364(6) Å, V = 8400(7) Å3, Z = 16, M = 552.26, ρcalcd = 1.747 g cm?3 μ = 3.828 mm?1, and F(000) = 4368. Complex II has a binuclear nine-coordinate pseudomonocapped square antiprismatic conformation and its crystal structure belongs to triclinic system and space P1 group. The crystal data are as follows: a = 9.7637(16), b = 9.9722(16), c = 12.945(2) Å, α= 85.853(2)°, β = 77. 140(2)°, γ = 77.140(2)°, V = 1198.4(3) Å3, Z = 1, M = 1340.80, ρcalcd = 1.858 g cm?3, μ = 3.380 mm?1, and F(000) = 674. As for complex III, it also has nine-coordinate mononuclear structure with distorted tricapped trigonal prism and its crystal structure belongs to monoclinic system andP21/c space group. The crystal data are as follows: a = 10.349(3), b = 12.760(4), c = 23.142(7) Å, β = 91.020(6)°, V = 3055.6(16) Å3, Z = 2, M = 797.55, ρcalcd = 1.734 g cm?3, μ = 2.674 mm?1, and F(000) = 1624. The results showed that although the ligands are different from one another in the shape and the numbers of coordination atoms, they all have nine-coordinate structures. However, one of them has binuclear structure and the other two have mononuclear structures because of the difference of the ligands. 相似文献
12.
L. B. Serezhkina E. V. Peresypkina M. O. Karasev A. V. Virovets V. N. Serezhkin 《Russian Journal of Inorganic Chemistry》2013,58(2):160-165
Cs3[UO2(CH3COO)3]2[UO2(CH3COO)(NCS)2(H2O)] (I) and Cs5[UO2(CH3COO)3]3[UO2 (NCS)4(H2O)] · 2H2O (II) have been synthesized via the reaction between uranyl acetate and cesium thiocyanate in aqueous solution. According to single-crystal X-ray diffraction data, both compounds crystallize in monoclinic system with the unit cell parameters a = 18.7036(5) Å, b = 16.7787(3) Å, c = 12.9636(3) Å, β = 92.532(1)°, space group C2/c, Z = 4, R = 0.0434 (I); and a = 21.7843(3) Å, b = 24.6436(5) Å, c = 13.1942(2) Å, β = 126.482(1)°, space group Cc, Z = 4, R = 0.0273 (II). Uranium-containing structural units of compound (I) are mononuclear [UO2(CH3COO)3]? and [UO2(CH3COO)(NCS)2(H2O)]? moieties, which correspond to the AB 3 01 and AB01M 3 1 crystallochemical groups (A = UO 2 2+ , B01 = CH3COO?, M1 = NCS? and H2O). The structure of compound II is built of [UO2(CH3COO)3]? and [UO2(NCS)4(H2O)]2? complexes, which belong to the AB 3 01 and AM 5 1 crystallochemical groups, respectively. Uranium-containing complexes in both structures are linked into a framework by hydrogen bonds and electrostatic interactions with cesium cations. The IR spectra of compounds I and II agree well with X-ray diffraction data. 相似文献
13.
1 INTRODUCTION The chalcogenidometallates with open frame- works have attracted considerable interest as pos- sible zeolite-like materials, of which highly interes- ting properties could be expected. Over the last de- cades a large number of thioanti… 相似文献
14.
M. Ishaque Khan Thomas Hope Sabri Cevik Chong Zheng Douglas Powell 《Journal of Cluster Science》2000,11(3):433-447
The synthesis and crystal structures of [H3NCH2CH2NH3][V2O6] (1) and [HN(CH2CH2)3NH][VV
2VIV
4O14]·H2O (2) are described. The structure of the oxidized compound 1 consists of parallel stacks of vanadium oxide chains of corner sharing {VO4} tetrahedra. The chains are stabilized by extensive hydrogen bonding involving oxide ligands of the chains and ethylenediammonium ions which fill the space between the stacks of chains. The structure of compound 2 consists of vanadium oxide layers separated by doubly protonated 1,4-diazabicyclo[2.2.2]octane and lattice water. The vanadium oxide layers, containing mixed-valence vanadium (VV and VIV) centers, are composed of zigzag ribbons of edge-sharing {VO5} square pyramids interconnected by {VO4} tetrahedra. Crystal data. C2H10N2O6V2 , 1: monoclinic, space group P21/c (No. 14), a=5.5359(5), b=12.9430(12), c=5.6856(5) Å, =90, =97.460(2), =90°, V=403.93(6) Å3, Z=2. A total of 2506 reflections (
max=27.89°) was collected, of which 954 were used to resolve the structure. The structure was solved by direct methods and least-squares refinement converged at R=0.0592. C6H16N2O15V6, 2: monoclinic, space group C2 (No. 5), a=19.303(4), b=6.667(2), c=7.579(2) Å, =90, =111.31(2), =90°, V=908.4(4) Å3, Z=2. A total of 1779 reflections was collected, of which 1591 unique reflections were used for structural elucidation. The structure was solved by direct methods and least-squares refinement converged at R=0.0314. 相似文献
15.
用X-射线衍射法测定了[C5H4C(CH3)(C3H7)CH2CH= CH2]NdMg2(μ3-OH)(μ3-Cl)(μ2-Cl)3(THF)4Cl的晶体结构。它属三斜晶系,空间群为P1- ,a= 12.698(3), b= 13.616(3), c= 13.712(3), α= 68.91(3), β= 84.34(3), γ= 63.07(3)°, V= 1966(1)3, Mr= 849.74, Dx= 1.412 g·cm - 3, μ= 1.7297 m m - 1, F(000)= 840, Z= 2, R= 0.073, w R= 0.086(I≥3σ(I))。分子中Nd(Ⅲ)原子的配位数为八,形成一个严重扭曲的八面体结构。两个Mg 原子的配位情况相似,它们的配位数都是六,构成两个扭曲的八面体。这三个八面体通过三个共用平面联接 相似文献
16.
The structure of double complex salts [Pd(NH3)3(NO2)][Rh(NH3)2(NO2)4] and [PdEn2][Rh(NH3)(NO2)5]·0.75H2O is determined by single crystal X-ray diffraction. In the structures, the main structural moieties are identified. 相似文献
17.
L. B. Serezhkina A. V. Vologzhanina N. A. Neklyudova V. N. Serezhkin M. Yu. Antipin 《Russian Journal of Inorganic Chemistry》2008,53(8):1193-1196
Single crystals of (NH4)2[(UO2)2C2O4(CH3COO)4] · 2H2O have been synthesized and studied. The compound crystallizes in the orthorhombic system with the unit cell parameters a = 6.9225(14) Å, b = 12.327(3) Å, c = 14.619(3) Å, space group Immm, Z = 2, and V = 1247.6(5) Å3. The main structural units of the crystals are the isle binuclear groups [(UO2)2C2O4(CH3COO)4]2? belonging to the crystal-chemical group A2K02B 4 01 (A = UO 2 2+ , K02 = C2O 4 2? , B01 = CH3COO?) of the uranyl complexes. The uranium-containing groups are linked into a three-dimensional framework due to electrostatic interaction with the ammonium cations and through a system of hydrogen bonds involving atoms of the water molecules, oxalate and acetate ions, and ammonium and uranyl cations. 相似文献
18.
The X-ray crystal structures of (NH4)2(15-crown-5)3[Cu(mnt)2] (1) and (NH4)2(benzo-15-crown-5)4- [Cu(mnt)2]·0.5H2O (2) were determined. Two single crystals are composed of distinct structures of ammonium-crown ether supramolecular cation and [Cu(mnt)2]2- anion. The triple-decker dication in complex 1 and a sandwich dimmer in complex 2 were observed. X-Band EPR studies on the single crystals of both complex 1 and complex 2 have been carried out at room temperature, which revealed that complex 2 showed a perfect hyperfine structure of Cu whereas that of complex 1 could not be observed. The principal values and direction cosines of the principal axes of the g and A tensors were computed by a least-squares fitting procedure. The spin density of Cu(Ⅱ) was estimated according to the principal values of the A tensors and compared well with the results calculated based on DFT method. 相似文献
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《Solid State Sciences》2003,5(7):1041-1046
The salt para methyl phenyl dimethyl ammonium tetrachloroantimonate (III) crystallizes in the monoclinic system with space group Cc. The unit cell dimensions are: a=13.780(1) Å, b=14.943(2) Å, c=8.192(1) Å, β=113.39(1)°, with Z=4. The structure consists of ammonium cations and polynuclear anions in which distorted SbCl5 square pyramids sharing a common Cl atom are held together in infinite chains parallel to the c axis. These chains are themselves interconnected by means of the NH⋯Cl hydrogen bonds. Differential scanning calorimetry study was carried out. The Raman of polycrystalline samples have been recorded at different temperatures between 77 and 300 K. A low-temperature phase transition at 230 K of order-disorder type was found. 相似文献