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1.
Nicholas C. Norman A. Guy Orpen Michael J. Quayle George R. Whittell 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(3):m160-m161
Crystals of the title compound, [NiCl(C18H15P)2], contain one molecule per asymmetric unit with no short intermolecular interactions. This is noteworthy since previous studies have reported that the formally 15‐electron species oligomerizes in the solid state. The nickel(I) centre has a distorted trigonal–planar coordination geometry, the origin of which is suggested to be electronic in nature. 相似文献
2.
Manuel Bardají Antonio Laguna M. Dolores Villacampa 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(11):e487-e488
The cation of the title compound, [Au4(PPh2CH2PPhCH2PPh2)2Cl2][Au(C6F5)3Cl]2 or [Au4Cl2(C32H29P3)2][AuCl(C6F5)3]2, displays a rhomboidal geometry for the Au atoms, with short Au?Au distances of 3.104 (2) and 3.185 (1) Å; the linear coordination at the AuI atoms is distorted: P—Au—P 164.7 (2)° and P—Au—Cl 170.67 (11)°. The anion shows the expected square‐planar geometry at AuIII, with the Au atom 0.022 (5) Å out of the plane of the four donor atoms. 相似文献
3.
Dianne D. Ellis Anthony L. Spek 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(12):e547-e548
In the title compound, [Ag{P(C6H5)}4][B{P(C6H5)}4]·CH3CN, the Ag ion resides on a crystallographic twofold rotation axis and is tetrahedrally coordinated. There is a disparity between the two independent Ag—P distances. This is due, in part, to the temperature differences (all previous determinations are at room temperature) but also to the packing effects of various anions. 相似文献
4.
Kenneth W. Henderson Alan R. Kennedy Arlene E. McKeown Robert E. Mulvey 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(6):674-675
The title complex, [ZrCl2(C4H8O)2(C14H14N)2]·0.5C7H8, was prepared in an unusual manner by utilizing [Mg{N(CH2Ph)2}2] as a ligand transfer reagent. The Zr atom lies in a distorted octahedral environment where steric repulsion from the large dibenzylamino ligands leads to a widening of the N—Zr—N angle [99.95 (9)°] and corresponding compression of other angles [Cl—Zr—Cl 160.95 (3)° and O—Zr—O 78.22 (7)°]. This distortion is compared with those found in the previously determined structures of the dimethylamino and diethylamino analogues. 相似文献
5.
Robert McCrindle Alan J. McAlees Erle Zang George Ferguson 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(4):e132-e133
The synthesis and X‐ray structural analysis of the title compound, [PdCl2(C3H7N)(C18H15P)]·C3H6O, are described. The crystal structure contains discrete monomeric molecules of the carbene complex and solvent molecules separated by normal van der Waals distances. The Pd atom is four‐coordinate in an essentially square‐planar environment, with the chlorine ligands mutually cis; Pd—P = 2.2495 (7), Pd—Cl = 2.3508 (7) and 2.3600 (7), Pd—C 1.948 (2) and N—C(carbene) 1.274 (3) Å. 相似文献
6.
Stefanus Otto 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(7):793-795
The crystal structure of the title compound, [PtCl(CH3)(C18H33P)2], is isostructural with various platinum(II) and palladium(II) complexes containing two bulky tricyclohexylphosphine ligands in a trans orientation. The Pt atom resides on an inversion centre, resulting in a 50% statistical disorder in the chloro and methyl positions. The most significant geometrical parameters are Pt—P 2.3431 (8), Pt—Cl 2.440 (4) and Pt—C1 2.179 (13) Å, and P—Pt—P 180, P—Pt—Cl 89.15 (12) and 90.85 (12), and C—Pt—Cl 172.7 (5)°. The effective and Tolman cone angles for the tricyclohexylphosphine ligands were calculated as 160 and 162°, respectively. 相似文献
7.
Cara L. Nygren M. E. T. Bragg John F. C. Turner 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(7):m275-m276
In the title compound, [K(C4H8O)][ZrCl2(C12H8N)3(C4H8O)], the Zr atom is pseudo‐octahedral, with two Cl ligands in trans positions. There is extensive interaction between the potassium cation and two of the aromatic carbazolyl ligands in η6 [C⃛K = 3.167 (3)–3.331 (3) Å] and η2 [C⃛K = 3.147 (3)–3.268 (2) Å] fashions. 相似文献
8.
Ilia A. Guzei Jeffrey S. Dougan Paul M. Treichel 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(9):1060-1061
The title compound, C36H30NP2+·HSO4?·CHCl3, consists of discrete ions and well separated chloroform solvate molecules. The central feature of the structure is O—H?O hydrogen bonding between two hydrogensulfate ions related by a crystallographic inversion centre. The chloroform solvate molecule takes part in a well defined C—H?O hydrogen bond. 相似文献
9.
Maria H. Johansson Stefanus Otto 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(1):e12-e15
Two different crystals (A and B) were used to structurally characterize trans‐[PtCl2(PPh3)2] and to study random and systematic errors in derived parameters. The compound is isomorphous with trans‐[PdCl2(PPh3)2] and with one of the polymorphs of trans‐[PtMeCl(PPh3)2] reported previously. Half‐normal probability plot analyses based on A and B show realistic s.u.'s and negligible systematic errors. R.m.s. calculations give very good agreement between A and B, 0.0088 Å. Important geometrical parameters are Pt—P = 2.3163 (11) Å, Pt—Cl = 2.2997 (11) Å, P—Pt—Cl = 87.88 (4) and 92.12 (4)°. Half‐normal probability plots and r.m.s. calculations were also used to compare the title compound with the palladium analogue, showing small systematic differences between the compounds. The torsion angles around the Pt—P bond were found to be very similar to those reported for isomorphous complexes, as well as to the torsion angles around the Pt—As bond in trans‐[PtCl2(AsPh3)2]. The NMR coupling constants for the title compound are similar to Pt—P coupling constants reported for analogous trans complexes. 相似文献
10.
Abdul Hamid Othman Yang‐Yi Yang Xiao‐Ming Chen Seik Weng Ng 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(8):e318-e319
The three‐coordinate Ag atom in the title compound, [Ag(C7H3N2O6)(C18H15P)2], shows trigonal–planar coordination [P—Ag—P = 147.1 (1)° and ΣAg = 359.0 (3)°]. Adjacent molecules are linked through the O atoms of adjacent nitro groups [Ag?O = 3.205 (3) and 3.302 (4) Å] into a zigzag chain running parallel to the c axis. 相似文献
11.
Huanrong Li Yingming Yao Qi Shen Linhong Weng 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(8):887-888
The title complex, [La2(C6H7)4(C6H5S)2(C4H8O)2]·2C4H8O, is a centrosymmetric dimer bridged through the S atoms of the benzenethiolate ligands. The bridging La2S2 unit is completely planar, while the geometry around the nine‐coordinate La atom is that of a distorted trigonal bipyramid. The La—S—La and S—La—S angles are 117.51 (4) and 62.5 (1)°, respectively, and the average La—S bond length is 2.9759 Å. The crystals contain two tetrahydrofuran solvate molecules for every complex molecule. 相似文献
12.
Diego Venegas‐Yazigi A. B. P. Lever Alan J. Lough Andrs Vega Vernica Paredes‐García Ramn Latorre Juan Costamagna 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(8):e323-e324
The Ru atom in the title compound, [Ru(C6H5CN)2{P(C6H5)3}{C6H4(NH)2}(H2O)](BF4)2·H2O, has six‐coordinate octahedral geometry, with a trans arrangement of the triphenylphosphine ligand and the water molecule. The asymmetric unit contains one complex cation, two tetrafluoroborate anions and one solvent water molecule, which is disordered over two sites (ratio of occupancies 0.70:0.30). 相似文献
13.
Fangfang Jian Fengli Bei Lude Lu Xujie Yang Xin Wang Ibrahim Abdul Razak S. Shanmuga Sundara Raj Hoong‐Kun Fun 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(7):e288-e289
In the title compound, [Cu(C5H10NO2S2)(C18H15P)2]·C18H15P, the Cu atom is in a distorted tetrahedral coordination, with two triphenylphosphine P atoms and two S atoms from an N,N‐bis(2‐hydroxyethyl)dithiocarbamate ligand occupying the vertices. The crystal structure is characterized by alternate layers of complex and triphenylphosphine molecules. 相似文献
14.
Magnus Magnussen Jesper Bendix 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(9):m342-m344
The title compound, mer‐[RuCl3N(C18H15As)2], is the first structurally characterized example of a nitride complex in which ruthenium is six‐coordinated to monodentate ligands only. The Ru[triple‐bond]N bond length [1.6161 (15) Å] is relatively long, and the trans influence of the nitride ligand is reflected by the difference between the Ru—Cltrans and Ru—Clcis bond lengths [0.1234 (4) Å]. The N—Ru—Cltrans axis is sited on a twofold axis. 相似文献
15.
Ming Li Maoyu Shang Hugues F. Duval W. Robert Scheidt 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(10):1206-1207
The precise structure of the title compound, [Fe2O(C44H24Br4N4)2]·2CH2Cl2, is reported. The Fe—N distances are non‐equivalent in pairs because of the asymmetric peripheral substitution; the values are 2.098 Å to the brominated rings and 2.041 Å to the other two rings. The Fe—O bond distance is 1.7583 (4) Å. The molecule has required twofold symmetry so that there is one unique porphyrin macrocycle and one Fe—O bond length in contrast to a previous report on the same species. 相似文献
16.
Alexander Filippou Peter Portius Athanassios Philippopoulos Gabriele Kociok‐Khn Burkhard Ziemer 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(9):e378-e379
trans‐[MoCl2(dppe)2] [dppe is 1,2‐ethanediylbis(diphenylphosphine), C26H24P2] was obtained as a side product from the reaction of trans‐[Mo(dppe)2(N2)2] with Cp*GeCl to give the germylyne complex trans‐[Cl(dppe)2Mo[triple‐bond]Ge(η1‐Cp*)]. The crystal structures of the hemipentane (0.5C5H12) and ditetrahydrofuran (2C4H8O) solvates of trans‐[MoCl2(dppe)2], (IIIa) and (IIIb), respectively, have been determined. 相似文献
17.
Belkacem Benmerad Achoura Guehria‐Laïdoudi Grald Bernardinelli Fadila Balegroune 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(3):321-323
The title compound, [La2(C3H2O4)3(H2O)4]·H2O, forms a layer‐type polymeric structure. The layers, which contain infinite puckered four‐membered La—O—La—O rings in a pseudo‐ternary symmetry, are formed by the lanthanum and one independent malonate group. They are interconnected by the second independent malonate group, giving a three‐dimensional framework in which wide channels accommodate one disordered water molecule of crystallization. The La atom lies on a twofold axis and is ten‐coordinated by eight O atoms from carboxylate groups and two water molecules. One malonate group is monodentate and triply bridging chelating, whilst the other is doubly monodentate. The extensive network of hydrogen bonds and bridge bonds observed in this structure enhances the structural stability. Despite some identical subfeatures, this structure is quite different from that observed in [La2(C3H2O4)3(H2O)3]·2H2O. 相似文献
18.
William Levason Elizabeth H. Newman Michael Webster 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(11):1308-1309
The title compound, [Ce(NO3)3(C2H6O)(C18H15OP)2], contains discrete molecules with nine‐coordinate Ce atoms having all nitrate groups bonded as symmetrical bidentate ligands [Ce—O(P) 2.369 (2) and 2.385 (2), Ce—O(N) 2.549 (3)–2.596 (3) and Ce—O(Et) 2.515 (3) Å]. 相似文献
19.
Zofia Olejnik Tadeusz Lis 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(11):1310-1311
The title compound, [Mn(CF3COO)2(H2O)4], crystallizes in the monoclinic space group C2/c. At about 215 K, it undergoes a reversible phase transition, which leads to crystal twinning. The crystal structure of the high‐temperature phase was determined at 220 K. The Mn2+ ion lies on a twofold axis and is octahedrally coordinated by two monodentate trifluoroacetate ligands in apical positions and by four equatorial aqua ligands, two of which lie on the twofold axis. Hydrogen‐bonding interactions connect the complex molecules, generating a three–dimensional network. 相似文献
20.
Fangfang Jian Lude Lu Xin Wang S. Shanmuga Sundara Raj Ibrahim Abdul Razak Hoong‐Kun Fun 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(8):939-940
In the crystal structure of the title complex, [Au(C7H14NS2)(C18H15P)2]·C4H10, the Au atom is in a distorted tetrahedral environment consisting of the two P atoms of the triphenylphosphine ligands and the two S atoms of the diisopropylthiocarbamate ligand. The molecular structure and packing are stablized by van der Waals interactions. 相似文献