共查询到20条相似文献,搜索用时 46 毫秒
1.
Sizwe J. Zamisa Patrick Ndungu Bernard Omondi 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(10):1100-1103
The reaction of 4,4′‐bipyridine with copper acetate in the presence of 4‐nitrophenol led to the formation of the title compound, {[Cu(CH3COO)2(C10H8N2)]·C6H5NO3·2H2O}n. The complex forms a double‐stranded ladder‐like coordination polymer extending along the b axis. The double‐stranded polymers are separated by 4‐nitrophenol and water solvent molecules. The two CuII centres of the centrosymmetric Cu2O2 ladder rungs have square‐pyramidal coordination environments, which are formed by two acetate O atoms and two 4,4′‐bipyridine N atoms in the basal plane and another acetate O atom at the apex. The ladder‐like double strands are separated from each other by one unit‐cell length along the c axis, and are connected by the water and 4‐nitrophenol molecules through a series of O—H...O and C—H...O hydrogen‐bonding interactions and two unique intermolecular π–π interactions. 相似文献
2.
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
3.
Yu‐Mei Dai En Tang Jin‐Feng Huang Qiu‐Yan Yang 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(10):m349-m352
The asymmetric unit of the title compound, {[Cu(CO3)(C14H14N4)1.5]·0.5C14H14N4·5H2O}n, contains one CuII cation in a slightly distorted square‐pyramidal coordination environment, one CO32− anion, one full and two half 1,4‐bis(imidazol‐1‐ylmethyl)benzene (bix) ligands, one half‐molecule of which is uncoordinated, and five uncoordinated water molecules. One of the coordinated bix ligands and the uncoordinated bix molecule are situated about centers of symmetry, located at the centers of the benzene rings. The coordinated bix ligands link the copper(II) ions into a [Cu(bix)1.5]n molecular ladder. These molecular ladders do not form interpenetrated ladders but are arranged in an ABAB parallel terrace, i.e. with the ladders arranged one above another, with sequence A translated with respect to B by 8 Å. To best of our knowledge, this arrangement has not been observed in any of the molecular ladder frameworks synthesized to date. The coordination environment of the CuII atom is completed by two O atoms of the CO32− anion. The framework is further strengthened by extensive O—H...O and O—H...N hydrogen bonds involving the water molecules, the O atoms of the CO32− anion and the N atoms of the bix ligands. This study describes the first example of a molecular ladder coordination polymer based on bix and therefore demonstrates further the usefulness of bix as a versatile multidentate ligand for constructing coordination polymers with interesting architectures. 相似文献
4.
Xiao‐Min Hao Gang Chen Chang‐Sheng Gu Ji‐Wei Liu 《Acta Crystallographica. Section C, Structural Chemistry》2014,70(8):770-772
In the title coordination polymer, [Cd2(SO4)2(C13H8N4)(H2O)2]n, there are two crystallographically independent CdII centres with different coordination geometries. The first CdII centre is hexacoordinated by four O atoms of four sulfate ligands, one water O atom and one N atom of a 1H‐imidazo[4,5‐f][1,10]phenanthroline (IP) ligand, giving a distorted octahedral coordination environment. The second CdII centre is heptacoordinated by four O atoms of three sulfate ligands, one water O atom and two N atoms of one chelating IP ligand, resulting in a distorted monocapped anti‐trigonal prismatic geometry. The symmetry‐independent CdII ions are bridged in an alternating fashion by sulfate ligands, forming one‐dimensional ladder‐like chains which are connected through the IP ligands to form two‐dimensional layers. These two‐dimensional layers are linked by interlayer hydrogen bonds, leading to the formation of a three‐dimensional supramolecular network. 相似文献
5.
Di Sun Geng‐Geng Luo Rong‐Bin Huang Na Zhang Lan‐Sun Zheng 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(8):m305-m307
The title compound, {[Ag(C4H6NO4)(C4H5N3)]·H2O}n, was synthesized by the reaction of silver(I) nitrate with 2‐aminopyrimidine and iminodiacetic acid. X‐ray analysis reveals that the crystal structure contains a one‐dimensional ladder‐like AgI coordination polymer and that N—H...O and O—H...O hydrogen bonding results in a three‐dimensional network. The AgI centre is four‐coordinated by three N atoms from three different 2‐aminopyrimidine ligands and one O atom from one iminodiacetate ligand. Comparison of the structural features with previous findings suggests that the existence of a second ligand plays an important role in the construction of such polymer frameworks. 相似文献
6.
Wen‐Na Zhao Jian‐Wei Zou Qing‐Shen Yu 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(9):m443-m444
The title one‐dimensional chain nickel(II)–disulfide complex, [Ni(C14H8O4S2)(C5H5N)2(H2O)]n, has each NiII cation coordinated by two N atoms from two pyridine ligands, three carboxylate O atoms from two different dithiodibenzoate ligands and one O atom from a coordinated water molecule, in a distorted octahedral coordination geometry. Each dithiodibenzoate ion links two NiII cations through its carboxylate O atoms, making the structure polymeric. Hydrogen‐bond interactions between two shoulder‐to‐shoulder chains lead to the formation of a ladder‐like structure. 相似文献
7.
Da‐Hua Hu Wei Huang Kai Cui Yi‐Zhi Li Shao‐Hua Gou Ji‐Lin Yan 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(2):m91-m93
The title polymeric ladder complex, {[Cu2(C7H6NO2)2(C10H8N2)3(H2O)2](NO3)2·4H2O}n, has been synthesized and spectroscopically characterized. The polymeric nature of the compound involves two non‐equivalent 4,4′‐bipyridyl ligands acting as almost orthogonal bridges joining the metal coordination Jahn–Teller‐distorted octahedra, and forming ladders packed under the influence of hydrogen bonds involving the uncoordinated amino group of the p‐aminobenzoate ligand, the NO3− anion and the water molecules. 相似文献
8.
Miao Du Zhi‐Hui Zhang Yan‐Ping You 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(9):o574-o576
Co‐crystallization of hemimellitic acid (benzene‐1,2,3‐tricarboxylic acid) dihydrate (H3HMA·2H2O) with 4,4′‐bipyridine (4,4′‐bpy) affords the 1:1 co‐crystal benzene‐1,2,3‐tricarboxylic acid–4,4′‐bipyridine (1/1), H3HMA·4,4′‐bpy or C9H6O6·C10H8N2. Strong O—H⋯O hydrogen bonds connect the acid molecules to form a one‐dimensional zigzag chain, around which the 4,4′‐bpy components are fixed as arms via O—H⋯N interactions, resulting in a ladder motif. Through weak C—H⋯O non‐covalent forces, the resulting acid layers are extended into a three‐dimensional pillar‐layered architecture supported by rod‐like 4,4′‐bpy components. The influence on hydrogen‐bonding models is also discussed, with the discovery of an unexpected interaction motif that does not follow the routine hydrogen‐bonded hierarchical rule in the construction of an acid–base co‐crystal. 相似文献
9.
Shi‐Jie Li Wen‐Dong Song Dong‐Liang Miao De‐Yun Ma 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(4):m105-m107
In the centrosymmetric dinuclear anions of the title bimetallic complex, {[Mg(H2O)6][Cu2(C8H2NO7)2]·2H2O}n, each CuII ion is strongly coordinated by four O atoms in a distorted square‐planar geometry. Two of these O atoms belong to phenolate groups and the other two to carboxylate groups from 5‐nitro‐2‐oxidoisophthalate (L1) trianions, derived from 5‐nitrobenzene‐1,2,3‐tricarboxylic acid (O2N–H3L). The phenolate O atoms bridge the two CuII ions in the anion. In addition, each CuII cation interacts weakly with a symmetry‐related carboxylate O atom of an adjacent L1 ligand, giving a square‐pyramidal coordination geometry. The copper residue forms a ladder‐like linear coordination polymer via L1 ligands. The [Mg(H2O)6]2+ cations sit on centres of inversion. The polymeric anions, cations and free water molecules are self‐assembled into a three‐dimensional supramolecular network via O—H...O hydrogen bonds. 相似文献
10.
Vijayakumar N. Sonar Sean Parkin Peter A. Crooks 《Acta Crystallographica. Section C, Structural Chemistry》2012,68(10):o405-o407
In the title compounds, C10H8N2O2, (I), and C12H12N2O2, (II), the two carbonyl groups are oriented with torsion angles of −149.3 (3) and −88.55 (15)°, respectively. The single‐bond distances linking the two carbonyl groups are 1.528 (4) and 1.5298 (17) Å, respectively. In (I), the molecules are linked by an elaborate system of N—H...O hydrogen bonds, which form adjacent R22(8) and R42(8) ring motifs to generate a ladder‐like construct. Adjacent ladders are further linked by N—H...O hydrogen bonds to build a three‐dimensional network. The hydrogen bonding in (II) is far simpler, consisting of helical chains of N—H...O‐linked molecules that follow the 21 screw of the b axis. It is the presence of an elaborate hydrogen‐bonding system in the crystal structure of (I) that leads to the different torsion angle for the orientation of the two adjacent carbonyl groups from that in (II). 相似文献
11.
Adina Rotar Richard A. Varga Cristian Silvestru 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(8):m355-m356
The title compound, [Sn2(C9H12N)4O(OH)2], consists of two [2‐(Me2NCH2)C6H4]2SnOH units bridged by an O atom located on a twofold rotation axis. The unique Sn atom is six‐coordinated with a (C,N)2SnO2 octahedral core, as a result of the strong intramolecular N→Sn dative coordination trans to the Sn—O bonds [N—Sn—O = 170.24 (12) and 167.83 (10)°]. Owing to the presence of intermolecular H...phenyl contacts, the molecules are arranged in a ladder‐like structure. 相似文献
12.
pH Dependent Synthesis of NdIII Coordination Compounds Based on Bifunctional 5‐(4‐Pyridyl)tetrazole‐2‐acetic Acid
下载免费PDF全文
![点击此处可从《无机化学与普通化学杂志》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Meng Jie Cao Yue Kang Li Peng Peng Sun Chen Yi Zhang Jue Wang Qiao Yun Li Gao Wen Yang 《无机化学与普通化学杂志》2016,642(21):1218-1221
The NdIII coordination compounds [Nd(4‐pytza)3(H2O)2] · 2H2O ( 1 ) and [Nd(4‐pytza)2(H2O)4]Cl · 2H2O ( 2 ) [H4‐pytza = 5‐(4‐pyridyl)tetrazole‐2‐acetic acid] were synthesized by reactions of K4‐pytza and NdCl3 · 6H2O at different pH values. Single crystal X‐ray diffraction analysis reveals that 4‐pytza ligands in 1 in a μ1,3‐COO syn‐syn or μ1,1,3‐COO bridging mode coordinate to two central NdIII atoms to display a dinuclear unit, which is connected by one of these 4‐pytza ligands acting in end‐to‐end bridging mode to form a 1D ladder‐like chain. Different from 1 , each 4‐pytza in 2 with a μ1,3‐COO syn‐anti bridging mode coordinates to two NdIII atoms to display a 1D zigzag chain. Furthermore, the luminescence properties of 1 and 2 were investigated at room temperature in the solid state. 相似文献
13.
Christopher Glidewell John N. Low Susan A. McWilliam Janet M. S. Skakle James L. Wardell 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(2):o97-o99
In 2‐trifluoromethyl‐4‐nitroaniline, C7H5F3N2O2, (I), the molecules lie across a mirror plane in space group Pnma. The molecules are linked by paired N—H?O hydrogen bonds to form a C(8)[R(6)] chain of rings, pairs of which are linked into a molecular ladder by a single C—H?O hydrogen bond. The isomeric 3‐trifluoromethyl‐4‐nitroaniline, (II), has Z′ = 2 in space group P21/c. Each molecule is linked to four others by N—H?O hydrogen bonds to form sheets built from alternating R(12) and R(32) rings. 相似文献
14.
(2,9‐Dimethyl‐1,10‐phenanthroline‐κ2N,N′)(pyridine‐2,6‐dicarboxylato‐κ3O2,N,O6)copper(II) trihydrate
Ibrahim Uar Ahmet Bulut Orhan Büyükgüngr 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(11):m479-m481
The copper(II) centre in the mononuclear title complex, [Cu(C7H3NO4)(C14H12N2)]·3H2O, is surrounded by one bidentate 2,9‐dimethyl‐1,10‐phenanthroline (dmphen) ligand and one tridentate pyridine‐2,6‐dicarboxylate ligand, and exhibits a distorted square‐pyramidal geometry. The crystal packing involves both hydrogen‐bonding and π–π interactions. The solvent water molecules link monomers to one another through hydrogen‐bonding interactions, forming ladder‐like chains in the bc plane. Face‐to‐face and slipped π–π interactions also occur between dmphen rings of neighboring molecules and are responsible for interchain packing. 相似文献
15.
Zhe‐Hui Weng Zi‐Lu Chen Fu‐Pei Liang 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(1):m64-m66
The title compound, [Mn7(C2H2N3)8(C2H3O2)4(OH)2]n, is composed of centrosymmetric heptanuclear building units with the central Mn atom on an inversion center. In the building block, three MnII ions are held together by one μ3‐hydroxide group, two μ2‐triazolate (trz) ligands and two μ2‐acetate groups, forming an Mn3 cluster. Two Mn3 clusters are bridged by an Mn atom via two μ2‐trz ligands and two μ2‐O atoms from two acetate ions to construct a heptanuclear building block. The heptanuclear building units, lying parallel to each other along the b direction, form one‐dimensional ladder‐like chains and are further interlinked, resulting in a three‐dimensional framework through Mn—Ntrz bonds. 相似文献
16.
Radka Novotn Zdenk Trvní
ek 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(2):158-161
The asymmetric unit of the title compound, C6H5N3O, consists of discrete molecules of 9‐deazahypoxanthine [systematic name: 3H‐pyrrolo[3,2‐d]pyrimidin‐4(5H)‐one]. The structure displays N—H...O hydrogen bonding, connecting the molecules into centrosymmetric dimers. These dimers are then connected by N—H...N hydrogen bonds into a ladder‐like chain along the c axis. The secondary structure is stabilized by weak noncovalent contacts of the C—H...O and C—H...C types, as well as by π–π stacking interactions, which organize the structure into a zigzag architecture. 相似文献
17.
Biao Yan Hongya Li Haixia Ma Xiangrong Ma Zhiyong Sun Yajun Ma 《Acta Crystallographica. Section C, Structural Chemistry》2020,76(9):891-896
Bis(4,5‐diamino‐1,2,4‐triazol‐3‐yl)methane monohydrate (BDATZM·H2O or C5H10N10·H2O) was synthesized and its crystal structure characterized by single‐crystal X‐ray diffraction; it belongs to the space group P (triclinic) with Z = 2. The structure of BDATZM·H2O can be described as a two‐dimensional ladder plane with extensive hydrogen bonding and no disorder. The thermal behaviour was studied under non‐isothermal conditions by differential scanning calorimetry (DSC) and thermogravimetric/differential thermogravimetric (TG/DTG) methods. The detonation velocity (D) and detonation pressure (P) of BDATZM were estimated using the nitrogen equivalent equation according to the experimental density. A comparison between BDATZM·H2O and bis(5‐amino‐1,2,4‐triazol‐3‐yl)methane (BATZM) was made to determine the effect of the amino group; the results suggest that the amino group increases the hydrophilicity, space utilization and energy, and decreases the thermal stability and symmetry of the resulting compound. 相似文献
18.
Marijana estan Gerald Giester Berislav Peri 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(11):m595-m597
The synthesis and crystal structure of the mononuclear title compound, [Co(C2O4)(C10H8N2)2]·5H2O, is reported. The Co atom is six‐coordinated by two O atoms of a bidentate oxalate group and by four N atoms of two bipyridine ligands. The neutral [Co(C2O4)(C10H8N2)2] entities are connected by π–π stacking interactions of the aromatic systems into a two‐dimensional layer, interconnected through a ladder‐like hydrogen‐bonding pattern of solvate water molecules. 相似文献
19.
Hans Reuter Rüdiger Pawlak 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(7):804-805
In the solid state, the title compound, di‐μ‐hydroxo‐1:2κ2O;‐3:4κ2O‐dihydroxo‐1κO,4κO‐octakis(2‐methyl‐2‐phenylpropyl)‐1κ2C,2κ2C,3κ2C,4κ2C‐di‐μ3‐oxo‐1:2:3κ3O;2:3:4κ3O‐tetratin(IV), [Sn4O2(OH)4(C10H13)8], forms centrosymmetric dimeric [(Neophyl2SnOH)(Neophyl2SnOH)O]2 molecules (Neophyl = 2‐methyl‐2‐phenylpropyl), with an almost planar Sn–O framework that adopts a ladder‐type structure consisting of three four‐membered rings. The hydroxyl groups are shielded by the organic groups, which prevent them from further condensation and from the formation of hydrogen bonds. 相似文献
20.
Yuki Nakagawa Yukihiro Takahashi Jun Harada Tamotsu Inabe 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(4):400-402
In the ionic charge‐transfer (CT) complex composed of bis(ethylenedithio)tetrathiafulvalene (ET) and 2,3‐dichloro‐5,6‐dicyano‐p‐benzoquinone (DDQ), C10H8S8·C8Cl2N2O2, the donor and acceptor molecules both form centrosymmetric dimers associated by strong face‐to‐face π–π interactions. The disordered DDQ molecules form a one‐dimensional π‐stacked column, while the ET molecules form a two‐leg ladder through additional short S...S contacts between adjacent π–π‐bonded dimers. The crystal structure of ET–DDQ revealed in this study will provide a valuable example of the two‐leg spin ladder system, which has rarely been reported for ET‐based CT complexes. 相似文献