共查询到20条相似文献,搜索用时 138 毫秒
1.
Wiesława Wołodkiewicz Tadeusz Głowiak 《Monatshefte für Chemie / Chemical Monthly》2000,131(7):711-719
Summary. The reaction products of Co(II)-2,3- and -2,5-dichlorobenzoate with imidazole (1, 2; CoL
2⋯2imdċ2H2O, L=C7H3Cl2O, imd=imidazole) were characterized by their spectroscopic and thermochemical properties. The compounds crystallize in the monoclonic
system with space group = P21/c, a=13.848(3), b=12.841(3) ?, c= 7.064(2) ?, β=98.12 °, V=1243.5(4) ?3, Z=2 for 1 and space group =P21/n, a=13.293(3), b= 6.964(2), c=13.800(3) ?, β=108.92(3) °, V=1208.6(4) ?3, Z=2 for 2. The complexes lose their crystal water in one step at 333 K and subsequently decompose to CoO with intermediate formation
of Co3O4.
Received August 9, 1999. Accepted (revised) February 11, 2000 相似文献
2.
The two new compounds Mn(dien)2[MoS4] (1) and Mn(dien)2[Mo2O2S6] (2) (dien = diethylenetriamine) were prepared under solvothermal conditions. Both compounds were obtained as phase-pure products. The structures consist of new [Mn(dien)2]2+ cations and isolated tetrahedral [MoS4]2− (1) or [Mo2O2S6]2− (2) anions. Between the anions and the cations, hydrogen bonding is observed. Compound 1 crystallizes in the tetragonal space group I (a = 10.219(2), c = 9.259(2) ?, Z = 2), whereas 2 crystallizes in the monoclinic space group P21/c (a = 8.703(2), b = 18.390(4), c = 14.603(3) ?, β = 103.18(3)°, Z = 4). The thermal behaviour of the thiomolybdates was investigated using difference thermoanalysis (DTA) and thermogravimetry (TG). Both compounds decompose under argon with a single endothermic signal in the DTA curve (peak maximum: 252 (1) and 242°C (2)). 相似文献
3.
Summary. The two new compounds Mn(dien)2[MoS4] (1) and Mn(dien)2[Mo2O2S6] (2) (dien = diethylenetriamine) were prepared under solvothermal conditions. Both compounds were obtained as phase-pure products. The
structures consist of new [Mn(dien)2]2+ cations and isolated tetrahedral [MoS4]2− (1) or [Mo2O2S6]2− (2) anions. Between the anions and the cations, hydrogen bonding is observed. Compound 1 crystallizes in the tetragonal space group I (a = 10.219(2), c = 9.259(2) ?, Z = 2), whereas 2 crystallizes in the monoclinic space group P21/c (a = 8.703(2), b = 18.390(4), c = 14.603(3) ?, β = 103.18(3)°, Z = 4). The thermal behaviour of the thiomolybdates was investigated using difference thermoanalysis (DTA) and thermogravimetry
(TG). Both compounds decompose under argon with a single endothermic signal in the DTA curve (peak maximum: 252 (1) and 242°C (2)).
Received November 5, 2001. Accepted December 27, 2001 相似文献
4.
Compounds 4-(oxiran-2-ylmethoxy)benzoic acid (2) and 4-acetoxybenzoic acid (4) are synthesized by a new synthetic route and studied by X-ray crystallography. Compound 2 crystallizes in the monoclinic system, P21/n space group, a = 5.1209(2) ?, b = 30.3429(16) ?, c = 5.9153(3) ?, β = 96.725(3)°, V = 912.81(8) ?3, Z = 4. Compound 4 crystallizes in the triclinic system, P-1 space group, a = 7.3400(4) ?, b = 8.0819(3) ?, c = 15.6548(9) ?, α = 85.754(3)°, β = 84.268(2)°, γ = 70.023(3)°, V = 867.63(8) ?3, Z = 4. The crystal structure of 2 comprises two crystallographically independent molecules of the compound. In the crystal structures of 2 and 4, pairs of molecules form carboxyl dimers. 相似文献
5.
Yu. V. Kokunov Yu. E. Gorbunova V. V. Kovalev 《Russian Journal of Inorganic Chemistry》2009,54(10):1603-1610
New complex chlorides [ZnCl2(ODA)] (I) (ODA=oxydianiline, C12H12N2O) and [ZnCl2(H2O)2](Me4Pyz)2 (II) (Me4Pyz = 2,3,5,6-tetramethylpyrazine) were synthesized and crystallographically characterized. Crystals of I are monoclinic, space group C2/c, a = 22.682(2) ?, b = 12.646(1) ?, c = 9.951(1) ?, β = 93.23(2)°, V = 2849.7(5) ?3, ρcalc = 1.569 g/cm3, Z = 8. Structure I contains cyclic fragments consisting of two tetrahedral complexes (ZnCl2N2) and two coordinated bridging oxydianiline ligands. Crystals of II are monoclinic, space group P2(1)/c, a = 8.972(2) ?, b = 13.862(3) ?, c = 17.528(4) ?, β = 101.72(3)°, V = 2134.5(7) ?3, ρcalc = 1.384 g/cm3, Z = 4. In structure II, supramolecular pseudo-metallocycles are formed due to formation of hydrogen bonds O(w)-H…N between coordinated water molecules
and noncoordinated nitrogen atoms of tetramethylpyrazine molecules. 相似文献
6.
Summary. Two novel Er-Cr ion-pair complexes ([Er(DMA)3(H2O)4][Cr(CN)6] and [Er(MPL)4(H2O)3][Cr(CN)6]·2H2O; DMA = dimethylacetamide, MPL = 1-methyl-2-pyrrolidinone) have been synthesized. [Er(DMA)3(H2O)4][Cr(CN)6] crystallizes in the monoclinic system (space group P
c
) with a = 9.789(2), b = 11.263(2), c = 13.997(3)?, β = 105.66(3)°, V = 1485.9(5)?3, Z = 2; [Er(MPL)4(H2O)3][Cr(CN)6]·2H2O crystallizes in the monoclinic system (space group P21) with a = 9.447(2), b = 13.881(3), c = 14.673(3)?, β = 101.85(3), V = 1883.1(7)?3, Z = 2. X-Ray crystal diffraction analyses reveal that the two complexes form a hydrogen bonding network structure through the
CN group and H2O molecules. Variable temperature susceptibilities for the two complexes indicate that weak antiferromagnetic interactions
exist between cation and anion pairs through this hydrogen bonding network. 相似文献
7.
Carbohydrazide is prepared by reacting dimethyl carbonate with hydrazine hydrate. Its single crystal has been cultured with slow evaporation method. Its molecular structure and crystal structure have been determined by X-ray single crystal diffraction technique. The obtained results shows that the crystal belongs to Crystal system of Monoclinic, space group P2(1)/n with crystal parameters of a = 3.725(1), b = 8.834(2), c = 11.96(3), β = 91.97(1)°, V = 392.23(2) 3, Z = 4, D
c = 1.522 g/cm3, μ = 0.128 mm−1, F0 0 0) = 192. Based on the crystal data, we have also carried quantum chemistry calculations on the title compound using the B3LYP and MP2 method with cc-pVTZ basis set. The calculation results further demonstrate the molecular structure of title compound and its coordination properties. 相似文献
8.
Coordination polymers [Ag(Me4Pyz)] PF6(I) and [Ag2(Me4Pyz)3](BF4)2·H2O (II) have been synthesized, and their structures have been determined. The crystals of I are monoclinic, space group C2/c, a = 9.440(2) ?, b = 10.587(2) ?, c = 13.165(3) ?, β= 107.19(3)°, V = 1257.0(5) ?3, d = 2.056 g/cm3, Z = 4. The crystals of II are monoclinic, space group P21/n, a = 13.062(3) ?, b = 12.259(2) ?, c = 18.996(4) ?, β = 97.73(3)°, V = 3014.1(11)?3, ρ = 1.798 g/cm3, Z = 4. The structure of I is built of linear polymeric cations [Ag(C8H12N2)]
∞
+
and octahedral anions [PF6]−. Upon the interaction of tetramethylpyrazine molecule with Ag+ ions, intersecting polymeric chains [Ag(C8H12)]
∞
+
(1D polymer) are formed extending in mutually perpendicular diagonal directions. The structure of II consists of layers (2D polymers) formed by fused sixmembered rings. These rings consist of Ag+ ions linked by bridging ligands Me4Pyz.
Original Russian Text ? Yu.V. Kokunov, Yu.E. Gorbunova, 2007, published in Zhurnal Neorganicheskoi Khimii, 2007, Vol. 52,
No. 5, pp. 743–750. 相似文献
9.
M. M. Monchak A. V. Pavlyuk V. V. Kinzhibalo M. G. Mys’kiv 《Russian Journal of Coordination Chemistry》2009,35(6):405-410
The alkylation of ethylenediamine with allyl bromide in the presence of a fourfold (with respect to ethylenediamine) molar
amount of NaHCO3 in acetone with an ethanol admixture (15: 1) affords LBr2 · 2H2O (I), where L2+ is the N,N,N,N′,N′,N′-hexaallylethylenediaminium cation. Single crystals of complexes L[CuII(Br0.45Cl3.55)] (II), L[Cu4I(Br4.55Cl1.45)] (III), and L[Cu4IBr6] (IV) are prepared by ac electrochemical synthesis from an ethanolic solution of LBr2 · 2H2O, CuCl2 · 2H2O (or CuBr2) at copper wire electrodes. The crystal structures of compounds I–IV are determined by X-ray diffraction analysis. The crystals of complex I are monoclinic: space group P21/n, a = 8.544(3), b = 10.404(3), c = 13.350(4) ?, β = 97.29(3)°, V = 1177.2(6) ?3, Z = 2. The bromine anions in compound I are bonded to the L2+ cations and water molecules through hydrogen contacts (E)H…Br (E = O, C) of 2.57(3)–2.86(3) ?. The crystals of compounds
II–IV are triclinic: space group P
. For II: a = 8.762(4), b = 9.163(4), c = 16.500(6) ?, α = 95.62(4)°, β = 96.39(4)°, γ = 111.46(4)°, V = 1211.4(9) ?3, Z = 2; for III: a = 9.074(4), b = 9.435(4), c = 9.829(5) ?, α = 116.12(4)°, β = 104.14(4)°, γ = 100.22(4)°, V = 692.3(6) ?3, Z = 1; for IV isostructural III: a = 9.084(4), b = 9.404(4), c = 9.869(4) ?, α = 116.31(3)°, β = 104.00(3)°, γ = 100.37(3)°, V = 692.1(5) ?3, Z = 1. Unlike the isolated tetrahedral CuX42− anion in structure II, an original chain anion (Cu4X62−)
n
is observed in the structures of π complexes III and IV.
Original Russian Text ? M.M. Monchak, A.V. Pavlyuk, V.V. Kinzhibalo, M.G. Mys’kiv, 2009, published in Koordinatsionnaya Khimiya,
2009, Vol. 35, No. 6, pp. 414–419. 相似文献
10.
B. K. Kasenov E. S. Mustafin M. A. Akubaeva S. T. Edil’baeva Sh. B. Kasenova Zh. I. Sagintaeva S. Zh. Davrenbekov 《Russian Journal of Inorganic Chemistry》2010,55(9):1454-1457
Manganites DyM3IMg3Mn4O12 and DyM3IBa3Mn4O12 (MI = Li, Na, K) were synthesized by the solid-state reaction of dysprosium and manganese(III) oxides and magnesium and corresponding alkali metal carbonates. The X-ray powder diffraction studies showed that the crystals
are orthozhombic with the following unit cell parameters and densities: DyLi3Mg3Mn4O12—a = 10.88 ?, b = 10.73 ?, c = 19.63 ?, V
0 = 1656.2 ?3, Z = 8, ρcalc = 5.36 g/cm3, ρpycn = 5.11 ± 0.05 g/cm3; DyNaMg3Mn4O12—a = 10.55 ?, b = 10.72 ?, c = 18.28 ?, V
0 = 2067.4 ?3, Z = 8, ρcalc = 4.60 g/cm3, ρpycn = 4.88 ± 0.09 g/cm3; DyK3Mg3Mn4O12—a = 10.56 ?, b = 10.72 ?, c = 20.89 ?, V
0 = 2206.0 ?3, Z = 8, ρcalc = 4.60 g/cm3, ρpycn = 4.92 ± 0.06 g/cm3; DyLi3Ba3Mn4O12—a = 10.53 ?, b = 10.69 ?, c = 21.28 ?, V
0 = 2395.4 ?3, Z = 8, ρcalc = 5.58 g/cm3, ρpycn = 5.98 ± 0.12 g/cm3; DyNa3Ba3Mn4O12—a = 10.53 ?, b = 10.74 ?, c = 23.00 ?, V
0 = 2602.3 ?3, Z = 8, ρcalc = 5.39 g/cm3, ρpycn = 5.30 ± 0.07 g/cm3; DyK3Ba3Mn4O12—a = 10.52 ?, b = 10.75 ?, c = 25.69 ?, V
0 = 2905.2 ?3, Z = 8, ρcalc = 5.04 g/cm3, ρpycn = 5.00 ± 0.18 g/cm3. 相似文献
11.
R. Lalrempuia Patrick J. Carroll Mohan Rao Kollipara 《Journal of Chemical Sciences》2004,116(1):21-27
The reaction of [(η
6-p-cymene)Ru(μCl)2Cl2] with functionalized phosphine viz, diphenyl-2-pyridylphosphine yielded complexes of the type: (a) P-bonded complex [(η
6-p-cymene)RuCl2(PPh2Py)] (1), (b) P-, N-chelated complex [(η
6-p-cymene)RuCl-(PPh2Py)]BF4 (2) and [RuCl2(PPh2Py)2] (3) resulting from the displacement of thep-cymene ligand. These complexes were characterized by1H NMR,31P NMR and analytical data. The structures of complexes1 and2 have been confirmed by single crystal X-ray diffraction study. Complex1 crystallised in triclinic space groupP 1 witha = 10.9403 (3) ?,b= 13.3108 (3) ?,c= 10-5394 (10) ?, α=88.943 (2)°, β = 117.193 (2)°, γ= 113.1680 (10)°, Z=2 andV= 1230.39 (5) ?3. The complex2 crystallises in monoclinic space group P21 witha = 9.1738 (4) ?,b = 14.0650 (6) s, c = 10.7453 (5) ?, β= 106.809 (1)°, Z = 2 andV= 1327.22 (10) ?3 相似文献
12.
Susana H. Tarulli Oscar V. Quinzani Oscar E. Piro Enrique J. Baran Eduardo E. Castellano 《Monatshefte für Chemie / Chemical Monthly》2001,29(5):779-787
The crystal structure of the title complex, [Cd(tsac)2(H2O)], has been determined by single crystal X-ray diffraction methods. It crystallizes in the monoclinic space group C2/c (a = 12.236(3), b = 8.919(3), c = 16.655(3) ?, β = 96.18(2)°, Z = 4). The molecular structure was solved from 1705 independent reflections with I > σ(I) and refined to R 1 = 0.0489. Infrared and Raman spectra of the complex were recorded and are briefly discussed. Its thermal behaviour was investigated by thermogravimetry and differential thermal analysis. 相似文献
13.
Susana H. Tarulli Oscar V. Quinzani Oscar E. Piro Enrique J. Baran Eduardo E. Castellano 《Monatshefte für Chemie / Chemical Monthly》2001,132(7):779-787
Summary. The crystal structure of the title complex, [Cd(tsac)2(H2O)], has been determined by single crystal X-ray diffraction methods. It crystallizes in the monoclinic space group C2/c (a = 12.236(3), b = 8.919(3), c = 16.655(3) ?, β = 96.18(2)°, Z = 4). The molecular structure was solved from 1705 independent reflections with I > σ(I) and refined to R
1 = 0.0489. Infrared and Raman spectra of the complex were recorded and are briefly discussed. Its thermal behaviour was investigated by thermogravimetry
and differential thermal analysis.
Received December 18, 2000. Accepted February 19, 2001 相似文献
14.
S. B. Artemkina M. S. Tarasenko A. V. Virovets N. G. Naumov 《Russian Journal of Coordination Chemistry》2012,38(4):257-263
Heterometallic chloride complexes [Mo5NbI8Cl6]
n− (n = 2, 3) are synthesized. The crystal structures of their salts are determined: for (Ph4P)2[Mo5NbI8Cl6] (I), triclinic crystal system, spacegroup P
[`1]\bar 1, a = 10.9886(6), b = 11.4604(5), c = 13.4343(7) ?, α = 66.124(2), β = 86.892(2), γ = 86.490(2)°, Z = 1, V = 1543.35(13) ?3; and for (4-MePyH)5[Mo5NbI8Cl6]Cl2 (II), monoclinic crystal system, space group C2/m, a = 16.4937(4), b = 14.7335(3), c = 11.6534(3) ?, β = 99.8750(10)°, Z = 2, V = 2789.94(11) ? The geometric parameters of compounds I and II and the conditions for the formation of the complexes with the charges −2 and −3 are discussed. 相似文献
15.
Kosterina E. V. Troyanov S. I. Kemnitz E. Aslanov L. A. 《Russian Journal of Coordination Chemistry》2001,27(7):458-462
The reaction of Rb, Cs, or Tl carbonates with a solution of phosphorous acid gave crystalline acid phosphites RbH2PO3(I), CsH2PO3(II), and TlH2PO3(III). The crystal structures of the compounds were studied by a single-crystal X-ray diffraction analysis at 150 K: I, monoclinic system, a= 7.530(2) Å, b= 8.634(2) Å, c= 12.426(2) Å, = 102.46(3)°, V= 788.8(3) Å3, Z= 8, space group P21/c, R
1= 0.0409; II, monoclinic system, a= 7.930(2) Å, b= 8.929(2) Å, c= 13.163(3) Å, = 104.84(3)°, V= 900.9(4) Å3, Z= 8, space group P21/c, R
1= 0.0239; III, orthorhombic system, a= 6.603(1) Å, b= 6.785(1) Å, c= 8.836(2) Å, V= 395.9(1) Å3, Z= 4, space group Pna21, R
1= 0.0350. The PHO3tretrahedra in structures I–IIIare joined via hydrogen bonds into infinite zigzag-like chains [HPHO3]
n–
n, which form layers alternating with layers of metal cations. The layers of anionic chains are wavelike in Iand IIand planar in III. Apparently, IIIis not isostructural to Ior IIdue to the fact that Tl(I) has a stereochemically active pair of electrons. 相似文献
16.
P. E. Plyusnin E. Yu. Semitut I. A. Baidina S. V. Korenev 《Journal of Structural Chemistry》2011,52(2):383-388
The crystal structures of double complex salts [M(NH3)5Br][AuBr4]2·H2O (M = Ir, Rh) are determined by single crystal XRD. The compounds crystallize in the triclinic system, P-1 space group, Z = 4. Crystallographic characteristics: [Ir(NH3)5Br][AuBr4]2·H2O: a = 8.2982(3) ?, b = 15.3045(4) ?, c = 17.4378(6) ?, α = 73.064(1)°, β = 88.938(1)°, γ = 86.221(1)°, V = 2113.95(12) ?3, d
x = 4.419 g/cm3, R = 0.0469; [Rh(NH3)5Br][AuBr4]2·H2O: a = 8.2855(2) ?, b = 15.2881(3) ?, c = 17.4053(4) ?, α = 73.015(1)°, β = 88.913(1)°, γ = 86.267(1)°, V = 2104.08(8) ?3, d
x = 4.165 g/sm3, R = 0.0480. The crystal structure of [Ir(NH3)5Br]Br2 is determined. The compound crystallizes in the orthorhombic system, Pnma space group, Z = 4. Crystallographic characteristics: a = 13.8521(3) ?, b = 10.8570(2) ?, c = 6.9908(1) ?, V = 1049.31(3) ?3, d
x = 3.273 g/cm3, R = 0.0127. 相似文献
17.
G. Z. Kaziev A. V. Oreshkina S. Holguin Quinones A. F. Stepnova V. E. Zavodnik Antonio de Ita D. A. Alekseev 《Russian Journal of Coordination Chemistry》2010,36(12):887-890
The sodium hydrogen oxovanadate [Na2(H2O)8] 2H2[V10O28] · 4H2O was synthesized and studied by TGA, X-ray diffraction, and NMR and IR spectroscopy. The crystals are triclinic, space group
P
$
\bar 1
$
\bar 1
, a = 8.545(7) ?, b = 10.827(2) ?, c = 11.627(2) ?, α = 105.48(3)°, β = 99.38(3)°, γ = 101.29(3)°, V = 989.9(3) ?3, ρ(calcd) = 2,381 g/cm3, Z= 1. 相似文献
18.
S. A. Talipov M. T. Khonkeldieva L. Yu. Izotova Z. G. Tilyakov B. T. Ibragimov 《Journal of Structural Chemistry》2011,52(1):186-192
Gossypol forms stable solvates with 4- and 2-picolines at room temperature. The solvates are investigated by single crystal
X-ray diffraction and thermal analysis. Solvate crystals of gossypol with 4-picoline (1) have the 1:3 composition (gossypol:4-picoline) and crystallize in the P21/c space group. This substance is isostructural to a trisolvate of gossypol with pyridine. Solvate crystals of gossypol with
2-picoline (2) have the 1:4 composition (gossypol:2-picoline) and crystallize in the P-1 space group. The unit cell parameters for the investigated structures are as follows: 1 monoclinic crystals, C30H30O8·3C6H7N, a = 10.7530(1) ?, b = 20.7834(3) ?, c = 19.1166(2) ?, β = 95.537(1)°, V = 4252.32(9) ?3, M = 797.92, Z = 4, d
x = 1.246 g/cm3, and R = 0.0489 for 4102 reflections; 2 triclinic crystals, C30H30O8·4C6H7N, a = 11.467(1) ? b = 14.962(2) ?, c = 15.570(3) ?, α = 75.62(1)°, β = 69.83(1)°, γ = 79.58(1)°, V = 2414.6(7) ?3, M = 891.04, Z = 2, d
x = 1.226 g/cm3, and R = 0.0528 for 3779 reflections. The results of the single crystal XRD and thermal analysis confirm that gossypol with 4-picoline
forms a trisolvat, and a tetrasolvate with 2-picoline. The transition from 4-picoline to 2-picoline proves to change the type
of the host-guest association from one-dimensional to zero-dimensional, i.e., to lead to a new crystal structure. Desolvation
of compound 2 begins at a lower temperature than that for compound 1, which is explained by their different crystal structures. Keywords: gossypol, 4-picoline, 2-picoline, clathrate formation,
crystal structure. 相似文献
19.
A new 2D metal-organic coordination polymer [Cu(trtr)2]n (1) (Htrtr = 3-(1,2,4-triazolyl-4-yl)-1H-1,2,4-triazole) is synthesized through the hydrothermal reaction of Cu(ClO4)2 with Htrtr. The crystal structure of 1 is determined by a direct method from X-ray diffraction data (Rigaku Mercury CCD, MoK
α radiation). 1 crystallizes in the monoclinic C2/c space group with unit cell parameters: a = 14.158(2) ?, b = 9.8050(14) ?, c = 11.413(3) ?, β = 127.9870(10)°, V = 1248.7(4) ?3, Z = 4, D
calc = 1.775 g/cm3. 1 features a 2D grid based on the propagation of 28-membered rings, which is further fabricated into a 3D supramolecular framework
via the hydrogen bond linkage. The fluorescence of 1 shows a blue emission at 441 nm with a 14 nm red-shift compared to that of free Htrtr, which can be assigned to LMCT. 相似文献
20.
N. V. Kuratieva V. S. Tkach D. S. Suslov M. V. Bykov S. A. Gromilov 《Journal of Structural Chemistry》2011,52(4):813-815
A single crystal X-ray diffraction study is carried out for [Pd(P(i-Pr)3)2(acac)]BF4, T = 150(2) K. Crystal data: a = 10.2935(4) ?, b = 11.3591(5) ?, c = 13.8728(6) ?, α = 89.154(2)°, β = 68.448(1)°, γ = 85.032(1)°, P-1 space group, V = 1502.75(11) ?3, Z = 2, d
x = 1.354 g/cm3. 相似文献