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1.
Yun Guo Miao Zhang Liang Shen Ying-Ying Jin Zhi-Min Jin 《Crystallography Reports》2010,55(7):1194-1197
The reaction of 2,6-dimethylpyridine with SbCl3 and HCl affords the title compound, the structure of which is ascertained by X-ray diffraction. The unit cell consists of
one bridged Sb2Cl82− anion and two 2,6-dimethylpyridinium cations. The trivalent antimony ion is bonded not only directly to chlorine anions,
but also is coordinated with chlorine anions by secondary bonds. In the crystal, there exists infinite coordinated chains
of [Sb2Cl8]
n
2n− anions running along the a axis, which link 2,6-dimethylpyridinium cations by N-H…Cl hydrogen bonds. 相似文献
2.
N. S. Kozlova O. A. Busanov E. V. Zabelina A. P. Kozlova V. M. Kasimova 《Crystallography Reports》2016,61(3):474-478
Crystals of cerium-doped gadolinium–gallium–aluminum garnet have been grown by the Czochralski method. The transmission and reflection spectra of these crystals in the wavelength range of 250–800 nm have been obtained by optical spectroscopy. Refractive indices are calculated based on the measured Brewster angles, the experimental results are approximated using the Cauchy equation, and a dispersion dependence is obtained. 相似文献
3.
Thomas?W.?Vertrees Gwendolyn?Hoben Andrew?N.?Kobylivker Christopher?L.?Edwards Simon?G.?Bott Andrew?R.?Barron
The molecular structure of [(tBu)2Al(-OC6H5-2-Me)]2 has been determined. Both the ortho-tolyl methyl groups are oriented towards Al(2). The intramolecular steric interaction between the ortho-methyl groups and the tert-butyl ligands results in the geometry about the bridging oxygen being significantly distorted while the geometries about the aluminum centers show a distortion from tetrahedral that is less than the sterically less hindered [(tBu)2Al(-OPh)]2. Crystal data: group C2/c, a = 13.733(3) Å, b = 15.135(3) Å, c = 15.420(3) Å, = 104.24(3), V = 3106(1) Å3, Z = 4, R = 0. 0612, wR2 = 0.1787. 相似文献
4.
Ying Liu Bao Zhang Jian-Min Dou Da-Qi Wang Da-Cheng Li Lei Zhou 《Journal of chemical crystallography》2007,37(11):717-720
Abstract One new mononuclear manganese complex of [Mn(4,4′-bip)2(OH2)4](DBA) · 4H2O (1) (4,4′-bipyridine, 4,4′-bip; H2DBA, benzene-1,3-dicarboxylic acid) has been obtained from the hydrothermal reaction of MnCl2 · 4H2O, 4,4′-bipyridine and H2DBA in the solvent of H2O at 140 °C for 3 days, characterized by X-ray analysis, spectroscopic methods, and thermal analysis. Packing diagram shows
that the three-dimensional network was formed via hydrogen bonds and strong π–π interactions.
Graphical abstract
One Novel Three-dimensional Network Constructed from [Mn(4,4′-bip)
2
(OH
2
)
4
]
2+
Cations and DBA
2−
Anions via Hydrogen-bonding and π–π Interactions
Ying Liu, Bao Zhang, Jian-min Dou, Da-qi Wang, Da-cheng Li, Lei Zhou
One new mononuclear manganese complex of [Mn(4,4’-bip)2(OH2)4](DBA) · 4H2O (1) (4,4’-bipyridine, 4,4’-bip; H2DBA, benzene-1, 3-dicarboxylic acid) has been obtained and haracterized by X-ray analysis, spectroscopic methods, and thermal
analysis. Packing diagram shows that the three-dimensional network was formed via hydrogen bonds and strong π-π interactions.
相似文献
5.
D. Yu. Pushcharovskii E. V. Suleimanov M. Pasero S. Merlino A. V. Barinova E. V. Alekseev 《Crystallography Reports》2003,48(2):212-215
The crystal structure of the compound Sr(AsUO6)2 · 8H2O is determined by X-ray diffraction analysis (monoclinic system, sp. gr. Pc, unit-cell parameters a = 7.154(1) Å, b = 7.101(1) Å, c = 18.901(7) Å, β = 92.67(2)°, Z = 2). The structure is built by (001)-parallel [AsUO6]? layers formed by flattened square UO6 bipyramids and AsO4 tetrahedra. The neighboring layers are connected via SrO8 square antiprisms. The cavities of the polyhedral framework thus formed are occupied by H2O molecules. The displacements of the anion complexes by a half-translation with respect to one another along only one lattice period is a characteristic feature of this polymorphous modification of the uran-mica group. 相似文献
6.
Abstract
The six-membered heterocycle [Me2AlSb(t-Bu)2]3 was reacted with the strong Lewis-base 4-dimethylaminopyridine (dmap), yielding the first completely alkyl-substituted monomeric complex dmap–Al(Me2)Sb(t-Bu)2 1. 1 was characterized by NMR spectroscopy and single crystal X-ray diffraction. 1 is monoclinic, space group P2 1 /n with a = 9.9004(2) ?, b = 16.8166(3) ?, c = 13.8400(3) ?, β = 100.746(1)° and Z = 4. 相似文献7.
N. V. Somov F. F. Chausov R. M. Zakirova M. A. Shumilova V. A. Aleksandrov V. G. Petrov 《Crystallography Reports》2017,62(5):734-738
Aquanitrilotris(methylenephosphonato)dirubidium is a 3D coordination polymer with a layer structure. Space group \(P\bar 1\), Z = 2; a = 8.0380(3) Å, b = 9.0522(4) Å, and c = 10.7837(4) Å; α = 113.252(4)°, β = 105.391(3)°, and γ = 96.182(3)°. Rb atoms populate two symmetrically inequivalent positions with c.n. = 8 and 10; significant difference in O–Rb–O angles in the coordination polyhedra is indicative of the ionic type of Rb–O bonds. In the crystal packing, molecules are connected by not only coordination bonds but hydrogen bonds as well. 相似文献
8.
Yong Zhang Jian Zhou Ai-Bin Tang Guo-Qing Bian Jie Dai 《Journal of chemical crystallography》2010,40(6):496-500
Abstract
Two new thiostannates [M(tepa)]2(μ-Sn2S6) (tepa = tetraethylenepentamine, M = Fe2+ 1 and Co2+ 2) were prepared by solvothermal method. Compounds 1 and 2 are isostructural. Both the compounds crystallize in the tetragonal system, space group I41/a (no. 88) with the crystal parameters of 1: a = 25.683(2) ?, b = 25.683(2) ?, c = 9.9860(9) ?, V = 6,586.7(11) ?3, Z = 8, and 2: a = 25.742(3) ?, b = 25.742(3) ?, c = 9.8977(12) ?, V = 6,558.5(14) ?3, Z = 8. The Sn2S6 4− anion acts as a bidentate bridging ligand connecting two transition metal complex cations by trans terminal S atoms to form neutral centrosymmetric [M(tepa)]2(μ-Sn2S6) moieties. 相似文献9.
A. A. Kaminskii A. F. Konstantinova V. P. Orekhova A. V. Butashin R. F. Klevtsova A. A. Pavlyuk 《Crystallography Reports》2001,46(4):665-672
Monoclinic α-KRE(WO4)2 crystals are grown. Their structure is described in two crystallographic settings. The principal refractive indices are determined and the coefficients and characteristic wavelengths are used for calculating refractive indices by the Selmeyer formulas. The data on the anisotropic parametric Raman generation in these crystals under the picosecond pumping are discussed. 相似文献
10.
The crystal structure of nitrilotris(methylenephosphonato)potassium K[μ6-NH(CH2PO3)3H4]—a three-dimensional coordination polymer—was determined. The potassium atom is coordinated by seven oxygen atoms belonging to the six nearest ligand molecules, resulting in distorted monocapped octahedral coordination geometry. The complex contains the four-membered chelate ring K–O–P–O. The K–O chemical bond is predominantly ionic. Meanwhile, the bonds of the potassium atom with some oxygen atoms have a noticeable covalent component. In addition to coordination bonds, the molecules in the crystal packing are linked by hydrogen bonds. 相似文献
11.
Joseph M. Ellsworth Zeeshan M. Khaliq Kathryn L. Seward Mark D. Smith Hans-Conrad zur Loye 《Journal of chemical crystallography》2007,37(11):749-754
Abstract Three new isostructural coordination complexes, M(pca)3, where M = Co (1), Cr (2), or Rh (3) and 2-pyrazine-carboxylate (pca), have been synthesized solvothermally and characterized
by single crystal X-ray diffraction and powder X-ray diffraction. In structures 1-3, the pca ligand chelates to the metal
centers in a tris-chelating arrangement through proximal nitrogen and oxygen donor atoms. Structures 1-3 are monoclinic and
crystallize in the space group C2/C. In structure 1, a = 28.066(13) ?, b = 8.036(4) ?, c = 13.577(6) ?, and β = 90.2(10)°.
In structure 2 a = 28.318(3) ?, b = 8.089(4) ?, c = 13.792(12) ?, and β = 90.256(2)°. In structure 3, a = 28.679(4) ?, b = 8.051(13) ?,
c=13.847(2) ?, and β = 90.585(2)°.
Graphical Abstract Three new isostructural coordination complexes, M(pca)3, where M = Co, Cr, or Rh and 2-pyrazine-carboxylate (pca), have been synthesized solvothermally and characterized by single
crystal X-ray diffraction and powder X-ray diffraction.
相似文献
12.
O. V. Rudnitskaya E. K. Kultyshkina A. I. Stash A. A. Glukhova N. U. Venskovskiĭ 《Crystallography Reports》2008,53(4):608-612
The complex [(NH2)2CSSC(NH2)2]2[OsBr6]Br2 · 3H2O is synthesized by the reaction of K2OsBr6 with thiocarbamide in concentrated HBr and characterized using electronic absorption and IR absorption spectroscopy. Its crystal structure is determined by X-ray diffraction. The crystals are orthorhombic, a = 11.730(2) Å, b = 14.052(3) Å, c = 16.994(3) Å, space group Cmcm, and Z = 4. The [OsBr6]2? anionic complex has an octahedral structure. The Os-Br distances fall in the range 2.483–2.490 Å. The α,α′-dithiobisformamidinium cation is a product of the oxidation of thiocarbamide. The S-S and C-S distances are 2.016 and 1.784 Å, respectively. The H2O molecules, Br?ions, and NH2 groups of the cation are linked by hydrogen bonds. 相似文献
13.
Saeed Ahmad Muhammad Nawaz Tahir Hafza Mariyam Javaid Muhammad Monim-ul-Mehboob Muhammad Ashraf Shaheen Rashid Mahmood 《Journal of chemical crystallography》2012,42(4):401-404
Abstract
A cyanido-bridged Cu(II)–Ag(I) bimetallic complex, [Cu(Imidazole)4{Ag(CN)2}2] has been prepared and structurally characterized. The compound crystallizes in the orthorhombic space group Pmna. The crystal structure of the complex consists of trinuclear molecules made up of one [Cu(Imidazole)4]+2 and two [Ag(CN)2]− units. The trinuclear molecules are interlinked to each other through N–H–N and C–H–N hydrogen bonds. The Cu(II) ions are located on mirrors and assume distorted octahedral geometry with the basal plane consisting of four imidazole N-atoms. 相似文献14.
Abstract
A new 1D coordination polymer [Me4N]3{[Mn(L)][Nb6Cl12(CN)6]}·3MeCN·H2O (1) (L = acacen 2− = N,N′-bis(acetylacetone)-1,2-ethylenediimine) was synthesized from reaction between [Me4N]4[Nb6Cl12(CN)6] and [Mn(L)]Cl in acetonitrile. The crystal structure of 1 was determined from single-crystal X-ray diffraction analysis. Compound 1 crystallizes in the tetragonal system, space group I41/a (No. 88), a = 30.585(4), c = 27.348(6) ?, V = 25582(7) ?3, Z = 16. Its 1D framework consists of chains formed of metal clusters and Mn(L) complexes linked to each other by Nb–C≡N–Mn–N≡C–Nb linkages. The chains extend along the a and b crystallographic axes and are related to each other by 41 screw axis. The chains are held together by [Me4N]+ cations and solvent molecules located in channels running between the chains. 1 and the previously reported 1D coordination polymer [Me4N]3{[Mn(5-MeO-salen)][Nb6Cl12(CN)6]} (3) differ from each other in terms of their synthesis and their structural characteristics. 相似文献15.
Treatment of the labile cluster Os3(CO)10(CH3CN)2 with morpholine in benzene at 60°C afforded Os3(CO)10(μ-η2-NC4H6O)(μ-H) (1). Decarbonylation of 1 at 128°C gave Os3(CO)9(μ3-η2-NC4H6O)(μ-H) (2), which reacts with PPh3 at ambient temperature to give an addition product Os3(CO)9(μ-η2-NC4H6O)(PPh3)(μ-H) (3). Compound 1 reacted with PPh3 at 98°C to give the substitution product 4 which is an isomer of 3. The reaction of Ru3(CO)12 with morpholine in the presence of Me3NO in refluxing benzene at 80°C afforded Ru3(CO)9(μ3-η2-NC4H6O)(μ-H) (5). Compounds 1– 5 have been characterized by elemental analysis, infrared, 1H NMR, and mass spectroscopic data. The molecular structure of 1 has been determined by single crystal X-ray diffraction analysis. Compound 1 crystallizes in the monoclinic space group P2/c with a = 29.598(8) Å, b = 9.202(2) Å, c = 14.496(4) Å, β = 93.19(3)°, Z = 8, and V = 3942(2) Å3. Compound 1 consists of an isosceles triangle of osmium atoms with one elongated Os–Os edge, which is bridged by the hydride and the morpholine ligand. 相似文献
16.
The crystal structure of (HPhen)2S2O8 · 2H2O is studied using X-ray diffraction. The crystals are monoclinic, a = 23.716(5) Å, b = 10.220(2) Å, c = 13.103(3) Å, β = 128.03(2)°, V = 2501.6(9) Å3, Z = 4, space group C2/c, and R = 0.0745 for 1579 reflections with I > 2σ(I). The crystal is built of S2O 8 2? centrosymmetric anions, HPhen + cations, and molecules of crystallization water. Hydrogen bonds link the structural units into chains. Within a chain, stacking interactions are observed between the phenanthroline rings (the interplanar spacing between the rings is 3.8 Å, and the dihedral angle between their planes is 8°). The data of IR spectroscopy confirm the formation of the N(Phen)-H bond. 相似文献
17.
N. L. Sizova V. L. Manomenova E. B. Rudneva A. É. Voloshin 《Crystallography Reports》2007,52(5):884-888
The Vickers hardness of the (010) and (001) planes in (NH4)2Ni(SO4)2 · 6H2O (ANSH) crystals has been measured. Anisotropy hardness of the first kind is revealed for the (010) plane in ANSH. The hardness anisotropy coefficient k 2 was determined to be 1.5. The temperature dependence of the microhardness of the (001) face of ANSH crystals was investigated in the temperature range from 20 to 80°C. The character of fracture of the (100), (010), and (001) planes during indentation with a spherical indenter has been qualitatively determined. 相似文献
18.
The crystal structure of mineral bussenite, Na2Ba2Fe[TiSi2O7][CO3]O(OH)(H2O)F, found in the Khibiny massif (the Kola Peninsula) has been determined. The parameters of the triclinic unit-cell are a = 5.399(3) Å, b = 7.016(9) Å, c = 16.254(14) Å, α = 102.44(8)°, β = 93.18(6)°, γ = 90.10(7)°, sp. gr. \(P\bar 1\), R = 0.054 for 1418 reflections with |F| > 2.5σ(F). The mineral studied belongs to the family of layered titanosilicates, in which, unlike the sulfate-and phosphate-containing representatives of this family, the interlayer spaces are filled with carbonate groups. 相似文献
19.
V. L. Manomenova E. B. Rudneva L. F. Malakhova N. G. Furmanova A. É. Voloshin T. N. Smirnova 《Crystallography Reports》2007,52(5):918-922
Large single crystals of rubidium nickel hexahydrate Rb2Ni(SO4)2 · 6H2O (RNSH) of optical quality were grown for the first time. The atomic structure of RNSH crystals was refined. A comparative analysis of the crystal structures of (M 1+)2Ni(SO4)2 · 6H2O, where M 1+ is K, Rb, or Cs, was performed. The solubility curve of RNSH in water was measured. The optical and thermogravimetric properties of RNSH were investigated. The internal defect structure of RNSH crystals was studied by X-ray topography. 相似文献
20.
L. B. Serezhkina A. V. Vologzhanina E. S. Klynin A. A. Korlyukov I. K. Moiseev V. N. Serezhkin 《Crystallography Reports》2012,57(2):252-257
The compound [UO2(NO3)2(H2O)2] · 2C12H18O was synthesized and studied by IR spectroscopy and X-ray diffraction. The structure consists of the neutral island groups
[UO2(NO3)2(H2O)2], which belong to the crystal-chemical group AB
01
2
M
1
2 (A = UO2
2+, B
01 = NO3−, M
1 = H2O) of uranyl complexes, and 1-adamantyl methyl ketone molecules. The characteristic features of the association of the complexes
[UO2(NO3)2(H2O)2] and 1-adamantyl methyl ketone molecules in the crystal structure via hydrogen bonds are considered with the use of Voronoi-Dirichlet
polyhedra. 相似文献