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1.
Anna M. Plonka Debasis Banerjee John B. Parise 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(11):m335-m337
The title compound, [Mg2(C12H14O4)2]n, is the first example of an s‐block metal adamantanedicarboxylate coordination polymer. The asymmetric unit comprises two crystallographically unique MgII centers and two adamantane‐1,3‐dicarboxylate ligands. The compound is constructed from a combination of chains of corner‐sharing magnesium‐centered polyhedra, parallel to the a axis, connected by organic linkers to form a layered polymer. The two MgII centers are present in distorted tetrahedral and octahedral coordination environments derived from carboxylate O atoms. Tetrahedrally coordinated MgII centers have been reported in organometallic compounds, but this is the first time that such coordination has been observed in a magnesium‐based coordination polymer. The bond valance sums of the two MgII centers are 2.05 and 2.11 valence units, matching well with the expected value of 2. 相似文献
2.
Luigi R. Nassimbeni Hong Su 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(6):o319-o322
The structures of the inclusion compounds 4,4′‐(cyclohexane‐1,1‐diyl)diphenol–3‐chlorophenol (1/1) and 4,4′‐(cyclohexane‐1,1‐diyl)diphenol–4‐chlorophenol (1/1), both C18H20O2·C6H5ClO, are isostructural with respect to the host molecule and are stabilized by extensive host–host, host–guest and guest–host hydrogen bonding. The packing is characterized by layers of host and guest molecules. The kinetics of thermal decomposition follow the R2 contracting‐area model, kt = [1 − (1 − α)½], and yield activation energies of 105 (8) and 96 (8) kJ mol−1, respectively. 相似文献
3.
Shi Zhou Chuan‐Bi Li Qing‐Wei Wang Seik Weng Ng 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(7):m224-m226
In the title cadmium(II) complex, [Cd(C8H4O5)(C14H14N4)(H2O)]n, the 5‐hydroxybenzene‐1,3‐dicarboxylate (5‐OH‐1,3‐bdc) and 1,4‐bis(imidazol‐1‐ylmethyl)benzene (1,4,‐bix) ligands bridge water‐coordinated CdII atoms to generate a three‐dimensional network. Two carboxylate groups from different ligands function as O,O′‐chelates, while two imidazole N atoms from different ligands coordinate in a monodentate fashion, and one water molecule completes the seven‐coordinate pentagonal bipyramid around the CdII atom, in which the N atoms occupy the axial sites and the O atoms occupy the equatorial sites. The overall architecture is a twofold interpenetrated CdSO4‐type framework. The two crystallographically equivalent frameworks are linked by O—H...O hydrogen bonds between the water, hydroxy and carboxylate groups. 相似文献
4.
Magdalena Wilk Jan Janczak Veneta Videnova‐Adrabinska 《Acta Crystallographica. Section C, Structural Chemistry》2012,68(2):m41-m44
The rigid organic ligand (pyridine‐3,5‐diyl)diphosphonic acid has been used to create the title novel three‐dimensional coordination polymer, [Ca(C5H6NO6P2)2(H2O)]n. The six‐coordinate calcium ion is in a distorted octahedral environment, formed by five phosphonate O atoms from five different (pyridin‐1‐ium‐3,5‐diyl)diphosphonate ligands, two of which are unique, and one water O atom. Two crystallographically independent acid monoanions, L1 and L2, serve to link metal centres using two different coordination modes, viz.η2μ2 and η3μ3, respectively. The latter ligand, L2, forms a strongly undulated two‐dimensional framework parallel to the crystallographic bc plane, whereas the former ligand, L1, is utilized in the formation of one‐dimensional helical chains in the [010] direction. The two sublattices of L1 and L2 interweave at the Ca2+ ions to form a three‐dimensional framework. In addition, multiple O—H...O and N—H...O hydrogen bonds stabilize the three‐dimensional coordination network. Topologically, the three‐dimensional framework can be simplified as a very unusual (2,3,5)‐connected three‐nodal net represented by the Schläfli symbol (4·82)(4·88·10)(8). 相似文献
5.
Huan‐Yu Wang Li‐Hua Huo Shan Gao Jing‐Gui Zhao 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(2):m65-m67
In the title complex, {[Mn(C4O4)(C10H8N2)(H2O)]·H2O}n, each MnII ion has a distorted octahedral coordination formed by two N atoms of a 2,2′‐bipyridine ligand, three carboxyl O atoms of three different acetylenedicarboxylate ligands and one coordinated water molecule. The acetylenedicarboxylate ligands act in a tridentate mode connecting adjacent MnII ions and constructing a two‐dimensional structure which can be regarded as an unusual plywood‐like stacked network. 相似文献
6.
Ming‐Lin Guo Chen‐Hu Guo 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(8):m352-m354
The title complex, {[Zn(C8H3NO6)(H2O)3]·H2O}n, has a one‐dimensional chain structure. The two carboxylate groups of the dianionic 2‐nitroterephthalate ligand adopt mono‐ and bidentate chelating modes. The Zn atom shows distorted octahedral coordination, bonded to three O atoms from two carboxylate groups and three O atoms of three non‐equivalent coordinated water molecules. The one‐dimensional chains are aggregated into two‐dimensional layers through inter‐chain hydrogen bonding. The whole three‐dimensional structure is further stabilized by inter‐layer hydrogen bonds. 相似文献
7.
Xiao‐Min Hao Gang Chen Chang‐Sheng Gu Ji‐Wei Liu 《Acta Crystallographica. Section C, Structural Chemistry》2014,70(7):712-714
In the title coordination polymer, {[Cd(C6H8O4S)(C13H14N2)]·H2O}n, the CdII atom displays a distorted octahedral coordination, formed by three carboxylate O atoms and one S atom from three different 3,3′‐thiodipropionate ligands, and two N atoms from two different 4,4′‐(propane‐1,3‐diyl)dipyridine ligands. The CdII centres are bridged through carboxylate O atoms of 3,3′‐thiodipropionate ligands and through N atoms of 4,4′‐(propane‐1,3‐diyl)dipyridine ligands to form two different one‐dimensional chains, which intersect to form a two‐dimensional layer. These two‐dimensional layers are linked by S atoms of 3,3′‐thiodipropionate ligands from adjacent layers to form a three‐dimensional network. 相似文献
8.
Yong‐Fang Li Zi‐Hong Pan Tian‐Jun Lou 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(11):m516-m518
The title compound, {[Ag2(C10H14N4)2](ClO4)2}n, is a one‐dimensional coordination polymer formed by AgI atoms linearly bridged by 1,1′‐(butane‐1,4‐diyl)diimidazole molecules. The chains have a helical arrangement and pairs of chains are held together by the rarely reported ligand‐unsupported Ag—Ag interaction [2.966 (1) Å], which results in a double‐helix structure. The double helix contains twisted 24‐membered metallomacrocycles, which are composed of four Ag atoms and two ligands. The Ag atoms lie on twofold axes. 相似文献
9.
Jian‐Li Lin Yue‐Qing Zheng 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(12):m501-m503
In the title compound, [Cu2(C6H8O4)(C6H9O4)2(C10H8N2)2(H2O)2]n, the square‐pyramidally coordinated Cu atoms are bridged by both 4,4‐bipyridine and adipate ligands into ladder‐like chains, with exo‐orientated 5‐carboxypentanoate ligands pendant from both side rails. Half of the adipate ligand is related to the other half by inversion symmetry. Interchain O—H⋯O hydrogen bonds from the aqua ligands to the carbonyl O atoms of the 5‐carboxypentanoate ligands are responsible for the formation of two‐dimensional grid‐like (4,4)‐networks, which complete a twofold interpenetration. 相似文献
10.
The title complex, [Ag4(C7H5O3)2(C8H6N2)4(C7H6O3)4], lies about an inversion centre and has a unique tetranuclear structure consisting of four AgI atoms bridged by four N atoms from two 1,8‐naphthyridine (napy) ligands to form an N:N′‐bridge and four O atoms from two salicylate (SA) ligands to form an O:O′‐bridge. The Ag atoms have distorted octahedral coordination geometry. The centrosymmetric Ag4 ring has Ag—Ag separations of 2.772 (2) and 3.127 (2) Å, and Ag—Ag—Ag angles of 107.70 (4) and 72.30 (4)°. All SA hydroxy groups take part in intramolecular O—H⋯O hydrogen bonding. In the crystal packing, the napy rings are oriented parallel and overlap one another. These π–π interactions, together with weak intermolecular C—H⋯O contacts, stabilize the crystal structure. 相似文献
11.
Qing‐Wei Wang Xiu‐Yan Wang Ming Wang Bing‐Yang Li Xiao‐Yuan Ma 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(8):m276-m278
In the title coordination compound, [Mn(C8H10O4)(C14H14N4)(H2O)2]n, each MnII centre occupies an inversion centre. The 1,4‐bis(imidazol‐1‐ylmethyl)benzene (1,4‐bix) ligand and the trans‐cyclohexane‐1,4‐dicarboxylate dianion (chdc) both function in bridging modes, linking adjacent MnII centres into a two‐dimensional four‐connected (4,4) network. These two‐dimensional layers are stacked in a parallel mode. Hydrogen bonds between water molecules and carboxylate O atoms link neighbouring (4,4) networks, yielding a three‐dimensional α‐polonium net. 相似文献
12.
Eleonora Freire Ricardo Baggio 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(4):m164-m166
The present form of barium acetate, formulated as [Ba(C2H3O2)2(H2O)3]n, is the largest reported hydrate of the salt and this leads to a distinct structural behaviour setting it apart from the rest of the family. The compound is a linear polymer with a nine‐coordinate Ba(Oaqua)3(Oacetate)6 monomer unit. The non‐H part of the structure is ordered according to C2/m symmetry, while the disordered water H atoms only abide by this symmetry in a statistical sense. Each molecule is halved by a mirror plane bisecting the Ba centre, one water molecule and one acetate ligand, while containing the other acetate ligand. The chains are interconnected by a disordered water–water/acetate O—H...O hydrogen‐bonding network involving all water H atoms. The structure and stability of this phase are compared with the other known acetates of barium which differ in the degree of hydration. 相似文献
13.
Anwar Usman Ibrahim Abdul Razak Suchada Chantrapromma Hoong‐Kun Fun Varughese Philip A. Sreekanth M. R. Prathapachandra Kurup 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(11):o652-o654
The title compound, C16H17N5S, is in the thione form and crystallizes with two independent molecules in the asymmetric unit. In both molecules, the pentamethyleneimine five‐membered ring adopts an envelope conformation, and in one of the molecules this ring shows positional disorder. The thione S and hydrazine N atoms are in the Z configuration with respect to the C—N bond. 相似文献
14.
Amy L. Kopf Paul A. Maggard Charlotte L. Stern Kenneth R. Poeppelmeier 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(4):m165-m168
The novel title hybrid isomorphous organic–inorganic mixed‐metal dichromates, [Ni(Cr2O7)(C10H8N2)2] and [Cu(Cr2O7)(C10H8N2)2], have been synthesized. A non‐centrosymmetric three‐dimensional (4,6)‐net is formed from a linear chain of vertex‐linked [Cr2O]2− and [MN4O]2+ (M = Ni and Cu) units, which in turn are linked by the planar bidentate 4,4′‐bipyridine ligand through the four remaining vertices of the [MN4O]2+ octahedra. There are two such three‐dimensional nets that interpenetrate with inversion symmetry. 相似文献
15.
Mikhail S. Grigoriev Christophe Den Auwer Daniel Meyer Philippe Moisy 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(4):m163-m165
The basic units in the structure of the title compound, {[UO2(C6H7NO6)(H2O)2]·3H2O}n, are ribbons in which every UO22+ cation is coordinated in a monodentate manner to three tridentate‐bridging nitriliotriacetate dianions. Hydrogen bonds bind the ribbons into a three‐dimensional structure. 相似文献
16.
Wei Sun Yan‐Tuan Li Zhi‐Yong Wu Ning‐Yu Xiao 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(3):m111-m113
In the crystal structure of the title complex, [Ni2(C10H20N4O2)(C12H12N2)2](ClO4)2 or [Ni(dmaeoxd)Ni(dmbp)2](ClO4)2 {H2dmaeoxd is N,N′‐bis[2‐(dimethylamino)ethyl]oxamide and dmbp is 4,4′‐dimethyl‐2,2′‐bipyridine}, the deprotonated dmaeoxd2− ligand is in a cis conformation and bridges two NiII atoms, one of which is located in a slightly distorted square‐planar environment, while the other is in an irregular octahedral environment. The cation is located on a twofold symmetry axis running through both Ni atoms. The dmaeoxd2− ligands interact with each other via C—H⋯O hydrogen bonds and π–π interactions, which results in an extended chain along the c axis. 相似文献
17.
G. Prochniak V. Videnova‐Adrabinska 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(2):m103-m106
This study presents the coordination modes and two‐dimensional network of a novel strontium(II) coordination polymer, [Sr(C7H5O5S)2(H2O)3]n. The eight‐coordinate Sr2+ ion is in a distorted bis‐disphenoidal coordination environment, surrounded by four sulfonate and one carboxyl O atom from five benzenesulfonate ligands, two of which are symmetry unique, and by three O atoms from three independent aqua ligands. The compound exhibits a monolayer structure with coordination bonds within and hydrogen bonds between the layers. The μ4 acid ligand bridges the metal ions in two dimensions to form a thick undulating monolayer with a hydrophobic interior and hydrophilic surfaces. A second independent monoanion is arranged outward from both sides of the monolayer and serves to link adjacent monolayers via carboxyl–water and water–carboxyl hydrogen bonds. 相似文献
18.
Shan‐Shan Liu Shuai Yuan Hai‐Feng Lu Meng‐Zhen Xu Di Sun 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(6):610-612
The cation‐templated self‐assembly of 1,4‐bis(2‐methyl‐1H‐imidazol‐1‐yl)butane (bmimb) with CuSCN gives rise to a novel two‐dimensional network, namely catena‐poly[2,2′‐dimethyl‐1,1′‐(butane‐1,4‐diyl)bis(1H‐imidazol‐3‐ium) [tetra‐μ2‐thiocyanato‐κ4S:S;κ4S:N‐dicopper(I)]], {(C12H20N4)[Cu2(NCS)4]}n. The CuI cation is four‐coordinated by one N and three S atoms, giving a tetrahedral geometry. One of the two crystallographically independent SCN− anions acts as a μ2‐S:S bridge, binding a pair of CuI cations into a centrosymmetric [Cu2(NCS)2] subunit, which is further extended into a two‐dimensional 44‐sql net by another kind of SCN− anion with an end‐to‐end μ2‐S:N coordination mode. Interestingly, each H2bmimb dication, lying on an inversion centre, threads through one of the windows of the two‐dimensional 44‐sql net, giving a pseudorotaxane‐like structure. The two‐dimensional 44‐sql networks are packed into the resultant three‐dimensional supramolecular framework through bmimb–SCN N—H...N hydrogen bonds. 相似文献
19.
Xiao‐Dan Wang Guang‐Feng Hou Ying‐Hui Yu Jin‐Sheng Gao 《Acta Crystallographica. Section C, Structural Chemistry》2012,68(12):m336-m339
The title compound, {[Ni(C9H4O6)(C14H14N4)]·0.41H2O}n, exhibits a three‐dimensional hydrogen‐bonded supramolecular framework. The NiII cation is six‐coordinated in a distorted triangular prism defined by two N atoms from two 1,3‐bis(imidazol‐l‐ylmethyl)benzene (bix) ligands and four O atoms from two 5‐carboxybenzene‐1,3‐dicarboxylate (HBTC) dianions. The bix molecules and HBTC dianions both act as bidentate ligands, linking the NiII cations to form a one‐dimensional coordination polymer. A two‐dimensional wave‐like net is constructed by O—H...O hydrogen bonds linking adjacent chains. Partially occupied solvent water molecules fill the cavities and link these layers to form a three‐dimensional supramolecular structure via O—H...O hydrogen bonds. The title compound was also characterized by powder X‐ray diffraction and thermogravimetric analysis. 相似文献
20.
Jian‐Hai Luo Chang‐Cang Huang Xi‐He Huang Jin‐Gen Wang 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(3):m121-m122
The title compound, [Cu2Fe3(C5H5)3(C2H3O2)(C6H4O2)3(C3H7NO)2], belongs to the classic dimeric paddle‐wheel structure type. It is an unusual example in that it contains two different carboxylate groups, viz. ferrocenecarboxylate and acetate. With three ferrocenecarboxylate groups and only one acetate group bridging the two Cu centres, a noncentrosymmetric molecular arrangement results. 相似文献