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1.
Quan‐Zheng Zhang Can‐Zhong Lu 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(2):m78-m80
In the title compound, [Mn2(C7H6NO2)2(C2H3O2)2(C10H8N2)2], the two MnII atoms are each coordinated by one 2,2′‐bipyridyl molecule, one 4‐aminobenzoate ion and two acetate ions. The two Mn atoms exhibit different coordination environments: one is coordinated by two N and four O atoms, while the other is coordinated by two N and three O atoms. The two Mn atoms are bridged by two acetate ions in a syn–anti mode, with an Mn⋯Mn distance of 4.081 (1) Å. 相似文献
2.
Shu‐Mei Chen Can‐Zhong Lu Ya‐Qin Yu Quan‐Zheng Zhang Xiang He 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(9):m437-m439
A novel chain molybdenum compound, {[Mo2O6(C6H5NO2)]·H2O}n, which was synthesized under hydrothermal conditions, consists of an infinite rail‐like chain formed by molybdenum oxide units linked by zwitterionic nicotinic acid ligands. Each Mo atom is coordinated octahedrally by six O atoms and the MoO6 octahedra are linked to one another via edge‐sharing to produce a zigzag polymeric chain, with nicotinic acid ligands located, alternately, on each side of the rail‐like chain plane. 相似文献
3.
Yi‐Hang Wen Ye‐Yan Qin Jian Zhang Zhao‐Ji Li Jian‐Kai Cheng Yao Kang Yuan‐Gen Yao 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(8):m371-m372
The title compound, {[Cu(C10H8N2)(H2O)](C8H4O4)0.5·H2O}n, has been synthesized hydrothermally and characterized by single‐crystal X‐ray diffraction. The compound consists of nearly linear one‐dimensional chains of [Cu(4,4′‐bipy)(H2O)]nn+ cations (4,4′‐bipy is 4,4′‐bipyridyl), surrounded by isophthalate anions and free water molecules. Hydrogen‐bonding interactions involving cationic chains, isophthalate anions and free water molecules lead to the formation of a three‐dimensional network structure. 相似文献
4.
Mao‐Lin Hu Qian Miao Qian Shi Ming‐De Ye 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(9):m460-m464
In the two related polymeric title compounds, {[La2(sip)2(phen)2(H2O)3]·H2O}n [sip is the 5‐sulfonatoisophthalate trianion (C8H3O7S3−) and phen is 1,10‐phenanthroline (C12H8N2)], (I), and {[La(sip)(H2O)3]·H2O}n, (II), the lanthanum(III) ions are nine‐coordinate, with similar distorted monocapped square‐antiprism coordination geometry. The two crystal structures are very different. In (I), the sip anion acts as a pentadentate ligand, one of the coordinated water molecules lies on a twofold axis and further inversion, n‐glide and translation operations generate a two‐dimensional framework. In (II), the sip anion functions as a hexadentate ligand and a three‐dimensional network with trinuclear 24‐membered rings is developed via inversion, n‐glide, twofold‐screw and translation operations. Both structures also have extensive O—H⋯O hydrogen‐bonded networks and π–π interactions. 相似文献
5.
Qiong‐Hua Jin Xia Li Ying‐Quan Zou Kai‐Bei Yu 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(6):676-677
Each Eu3+ ion in the title compound, catena‐poly[europium(III)‐tri‐μ‐4‐methylbenzoato‐O:O,O′;O:O,O′;O,O′:O′], {[Eu(C8H7O2)3]3}n, is coordinated by nine O atoms, and three Eu atoms form a trimeric unit. These trimeric units are linked by bridging–chelating carboxylates to form an infinite one‐dimensional polymer chain. 相似文献
6.
Zhao‐Xun Lian Ping Liu Jia‐Min Zhang Tian‐Xi Wang Tian‐Jun Lou 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(11):m525-m527
In the title compound, [V4O8(SeO3)2(C10H8N2)4], there are two distinct vanadium coordination environments. Alternating corner‐shared VO4N2 octahedra and SeO3 pyramids result in eight‐membered centrosymmetric V2Se2O4 rings. In addition, pairs of V centres form centrosymmetric V2O6N4 clusters via edge‐sharing. These two kinds of secondary building units are linked in an ABABAB fashion to give an infinite chain whose nature is unprecedented in Se–V–O systems. 相似文献
7.
Xia Zhu Bao‐Zong Li Jun‐Hui Zhou Bao‐Long Li Yong Zhang 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(4):m191-m193
In the crystal structure of the title complex, [Zn(N3)2(C6H8N6)]n or [Zn(N3)2(bte)]n, where bte is μ‐1,2‐bis(1,2,4‐triazol‐1‐yl)ethane, each Zn atom is pentacoordinated in a distorted trigonal‐bipyramidal coordination environment involving two N atoms from two bte ligands and three N atoms from three azide ligands. The Zn atoms are bridged by μ‐1,1‐azide groups and bte ligands around a centre of inversion, forming an infinite one‐dimensional chain containing both four‐membered Zn(μ‐1,1‐N3)2Zn and 18‐membered Zn(gauche‐bte)2Zn rings. 相似文献
8.
Wei Su Wen‐Hua Bi Xing Li Rong Cao 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(1):m16-m18
The hydrothermal reaction of Cd(CH3COO)2·2H2O, 4,4′‐bipyridyl and 2‐sulfobenzoic acid produced the title compound, {[Cd2(C7H4O5S)2(C10H8N2)2(H2O)2]·2H2O}n, which forms a two‐dimensional coordination polymer, the sheets of which are linked via hydrogen bonds. Two different types of Cd atoms are present, one lying on a twofold rotation axis and the other on a centre of inversion. Similarly, there are two types of bipyridyl ligand present, one lying across a twofold rotation axis and the other across a centre of inversion. 相似文献
9.
In catena‐poly[[(di‐2‐pyridylamine‐κ2N,N′)silver(I)]‐μ‐nicotinato‐κ2N:O], [Ag(C6H4NO2)(C10H9N3)]n, the AgI atom is tetracoordinated by two N atoms from the di‐2‐pyridylamine (BPA) ligand [Ag—N = 2.3785 (18) and 2.3298 (18) Å] and by one N atom and one carboxylate O atom from nicotinate ligands [Ag—N = 2.2827 (15) Å and Ag—O = 2.3636 (14) Å]. Bridging by nicotinate N and O atoms generates a polymeric chain structure, which extends along [100]. The carboxyl O atom not bonded to the Ag atom takes part in an intrachain C—H⋯O hydrogen bond, further stabilizing the chain. Pairs of chains are linked by N—H⋯O hydrogen bonds to generate ribbons. There are no π–π interactions in this complex. In catena‐poly[[(di‐2‐pyridylamine‐κ2N,N′)silver(I)]‐μ‐2,6‐dihydroxybenzoato‐κ2O1:O2], [Ag(C7H5O4)(C10H9N3)]n, the AgI atom has a distorted tetrahedral coordination, with three strong bonds to two pyridine N atoms from the BPA ligand [Ag—N = 2.286 (5) and 2.320 (5) Å] and to one carboxylate O atom from the 2,6‐dihydroxybenzoate ligand [Ag—O = 2.222 (4) Å]; the fourth, weaker, Ag‐atom coordination is to one of the phenol O atoms [Ag⋯O = 2.703 (4) Å] of an adjacent moiety, and this interaction generates a polymeric chain along [100]. Pairs of chains are linked about inversion centers by N—H⋯O hydrogen bonds to form ribbons, within which there are π–π interactions. The ribbons are linked about inversion centers by pairs of C—H⋯O hydrogen bonds and additional π–π interactions between inversion‐related pairs of 2,6‐dihydroxybenzoate ligands to generate a three‐dimensional network. 相似文献
10.
Yi‐Ming Xie Ji‐Huai Wu 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(5):m220-m221
The title compound, [HgCl2(C10H8N2)]n, features two‐dimensional [HgCl2(4,4′‐bipy)]n neutral networks (4,4′‐bipy is 4,4′‐bipyridine), based on an octahedral Hg atom coordinated by four μ2‐Cl atoms and two μ2‐4,4′‐bipy ligands in trans positions, yielding a HgCl4N2 octahedron. The structure has mmm symmetry about the Hg atoms, with most of the atoms on at least one mirror plane, but the unsubstituted C atoms of the 4,4′‐bipy rings are disordered across a mirror plane. Photoluminescent investigations reveal that the title compound displays a strong emission in the green region, which probably originates from a ligand‐to‐ligand charge‐transfer transition. 相似文献
11.
Ming‐Liang Tong Xiao‐Ming Chen Seik Weng Ng 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(9):e374-e375
The Cu atom in the title complex {[Cu(C10H8N2)(C12H8N2)(ClO4)2]·H2O}n, has an N4O2 octahedral coordination geometry, the Cu atoms being bridged by the bipyridine and chelated by the phenanthroline heterocycles. Adjacent molecules are linked into a zigzag chain running along the c axis of the monoclinic unit cell. The chains are connected through lattice water molecules to produce a layer structure. 相似文献
12.
Zhong‐Lu You Hai‐Liang Zhu Wei‐Sheng Liu 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(12):m620-m622
The title compound, {[Ag2(C4H4N2)3](CF3SO3)2·2H2O}n, is a polymeric pyrazine–silver(I) complex. Each AgI ion is three‐coordinated by N atoms of three different pyrazine ligands, forming a T‐shaped coordination configuration. In the crystal structure, uncoordinated water molecules are linked to trifluoromethanesulfonate anions through intermolecular O—H⋯O hydrogen bonds. There are weaker Ag⋯O interactions involving the water and sulfonate O atoms. 相似文献
13.
Xia Li Ying‐Quan Zou Bo Zheng Huai‐Ming Hu 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(5):m197-m199
The title compound, [Eu(C9H9O4)3]n or [Eu(2,3‐DMOBA)3]n, where 2,3‐DMOBA is 2,3‐dimethoxybenzoate, is an infinite one‐dimensional non‐centrosymmetric coordination polymer. The unique EuIII atom is bridged by six carboxylate ligands; it is ennea‐coordinated and has a distorted tricapped trigonal prism geometry. The Eu—O distances are in the range 2.315 (3)–2.959 (5) Å. 相似文献
14.
Cheng‐Bing Ma Feng Chen Chun‐Xia Zhang Ming‐Qiang Hu Chang‐Neng Chen Qiu‐Tian Liu 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(6):m285-m287
The polymeric title complex, {[Mn(C4H4O4)(C10H8N2)(H2O)]·0.5C10H8N2}n, possesses a three‐dimensional open‐framework structure, with the solvate 4,4′‐bipyridine (bipy) molecules, which lie around centers of inversion, clathrated in the channels of the framework. The MnII center is surrounded by three succinate (succ) ligands, one water molecule and two bipy ligands, and displays a slightly distorted octahedral coordination environment, with cis angles ranging from 84.14 (12) to 96.56 (11)°. Each succ dianion coordinates to three MnII atoms, thus acting as a bridging tridentate ligand; in turn, the MnII atoms are bridged by three succ ligands, thus forming a two‐dimensional Mn–succ sheet pillared by the bridging bipy ligands. Two hydrogen‐bonding interactions, involving the water molecules and the carboxy O atoms of the succ ligands, are present in the crystal structure. 相似文献
15.
Yong Cui Jing Ren Gang Chen Weichao Yu Yitai Qian 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(12):e552-e553
The title complex, [PbBr2(bipy)]n (bipy is 4,4′‐bipyridine, C10H8N2), was obtained by hydrothermal reaction of Pb(O2CCH3), NaBr and bipy. The bipy group acts as a linear bifunctional bridge forming a planar {–[Pb(bipy)]–}n belt in the direction of the b axis. The remaining lead coordination sites are occupied by Br ions which link Pb centres in adjacent belts through double bridges to form extended two‐dimensional layers. 相似文献
16.
Alexander S. Lyakhov Pavel N. Gaponik Michail M. Degtyarik Ludmila S. Ivashkevich 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(6):m204-m206
In the polymeric title complex, [CuCl2(C3H6N4)2]n, there are two ligands in the asymmetric unit. The Cu atom adopts an elongated octahedral geometry, with two 2‐ethyltetrazole ligands [Cu—N = 2.0037 (16) and 2.0136 (16) Å] and two Cl atoms [Cu—Cl = 2.2595 (6) and 2.2796 (6) Å] in equatorial positions. A Cl atom and a symmetry‐related 2‐ethyltetrazole molecule [Cu—Cl = 2.8845 (8) Å and Cu—N = 2.851 (2) Å] lie in the axial positions of the octahedron. One of the two 2‐ethyltetrazole ligands of the asymmetric unit exhibits bidentate binding to two Cu atoms through two N atoms of the tetrazole ring, whereas the other ligand is coordinated in a monodentate fashion via one tetrazole N atom. The Cu‐atom octahedra form dimer entities by sharing edges with equatorial and axial Cl atoms. The dimers are linked together through the 2‐ethyltetrazole ligands to form one‐dimensional polymeric zigzag chains extending along the b axis. The chains are connected into infinite layers parallel to the (10) plane via the 2‐ethyltetrazole ligands. 相似文献
17.
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
18.
Dmitry O. Ivashkevich Alexander S. Lyakhov Dariya S. Pytleva Sergei V. Voitekhovich Pavel N. Gaponik 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(6):m221-m223
In the title compound, [Cu2Cl4(C6H10N8)2]n, the ligand has C2 symmetry, and the Cu and Cl atoms lie on a mirror plane. The coordination polyhedron of the Cu atom is a distorted square pyramid, with the basal positions occupied by two N atoms from two different ligands [Cu—N = 2.0407 (18) Å] and by the two Cl atoms [Cu—Cl = 2.2705 (8) and 2.2499 (9) Å], and the apical position occupied by a Cl atom [Cu—Cl = 2.8154 (9) Å] that belongs to the basal plane of a neighbouring Cu atom. The [CuCl2(C6H10N8)]2 units form infinite chains extending along the a axis via the Cl atoms. Intermolecular C—H⃛Cl contacts [C⃛Cl = 3.484 (2) Å] are also present in the chains. The chains are linked together by intermolecular C—H⃛N interactions [C⃛N = 3.314 (3) Å]. 相似文献
19.
Yu‐Ling Wang Qing‐Yan Liu Li Xu 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(7):m304-m307
The crystal structure of the title compound, {[Tm(C8H3O7S)(H2O)5]·1.5C10H8N2·0.5H2O}n, is built up from two [Tm(SIP)(H2O)5] molecules (SIP3− is 5‐sulfonatobenzene‐1,3‐dicarboxylate), three 4,4′‐bipyridyl (bpy) molecules and one solvent water molecule. One of the bpy molecules and the solvent water molecule are located on an inversion centre and a twofold rotation axis, respectively. The TmIII ion coordination is composed of four carboxylate O atoms from two trianionic SIP3− ligands and five coordinated water molecules. The Tm3+ ions are linked by the SIP3− ligands to form a one‐dimensional zigzag chain propagating along the c axis. The chains are linked by interchain O—H...O hydrogen bonds to generate a two‐dimensional layered structure. The bpy molecules are not involved in coordination but are linked by O—H...N hydrogen bonds to form two‐dimensional layers. The two‐dimensional layers are further bridged by the bpy molecules as pillars and the solvent water molecules through hydrogen bonds, giving a three‐dimensional supramolecular structure. π–π stacking interactions between the parallel aromatic rings, arranged in an offset fashion with a face‐to‐face distance of 3.566 (1) Å, are observed in the crystal packing. 相似文献
20.
Rajesh Koner Israel Goldberg 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(5):m185-m189
The title compounds, [Cu(CHO2)2(C10H8N2)]n, (I), and {[Cu(C10H4O5)(C12H12N2)(H2O)2]·2H2O}n, (II), are composed of one‐dimensional linear coordination polymers involving copper(II) ions and bidentate bipyridyl species. In (I), the polymeric chains are located on twofold rotation axes at (x, x, 0) and are arranged in layered zones centered at z = 0, , ½ and parallel to the ab plane of the tetragonal crystal. Weak coordination of the formate anions of one layer to the copper centers of neighboring layers imparts a three‐dimensional connectivity to this structure. In (II), the polymeric chains propagate parallel to the a axis of the crystal. Noncoordinated water molecules link the chains through O—H...O hydrogen bonding in directions perpendicular to c, imparting to the entire structure three‐dimensional connectivity. The metal ions adopt distorted octahedral and square‐based pyramidal environments in (I) and (II), respectively. This study indicates that, under the given conditions, extended coordination involves CuII centers associating with the bipyridyl ligands rather than with the competing benzofurandicarboxylate entities. 相似文献