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Catena-Poly[[di-?-chlorido-dicopper(I)]bis-[?-?,?-4-(2-allyl-2H-tetra-zol-5-yl)pyridine]].

ABSTRACT: The title polymer, [Cu(2)Cl(2)(C(9)H(9)N(5))(2)](n), has been prepared by the solvothermal treatment of CuCl with 4-(2-allyl-2H-tetra-zol-5-yl)pyridine. The crystal structure shows that the title compound is a homometallic Cu(I)-olefin coordination polymer, in which the Cu(2)Cl(2) nodes are bridged by two olefin ligands. The asymmetric unit contains one-half of the monomer, the complete monomer having twofold rotation symmetry. The coordination environment of Cu(I) is slightly distorted tetra-hedral, with coordination sites being two ?(2)-Cl atoms, one pyridine N atom of an organic ligand and one allylic double bond of a symmetry-related ligand. Each organic mol-ecule behaves as a bidentate ligand, connecting two neighboring Cu(2)Cl(2) dimers in the polymeric chain, which runs along [010].

SUBMITTER: Wang W

PROVIDER: S-EPMC2961636 | biostudies-literature | 2008 Jun

REPOSITORIES: biostudies-literature

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catena-Poly[[di-μ-chlorido-dicopper(I)]bis-[μ-η,σ-4-(2-allyl-2H-tetra-zol-5-yl)pyridine]].

Wang Wei W

Acta crystallographica. Section E, Structure reports online 20080619 Pt 7

The title polymer, [Cu(2)Cl(2)(C(9)H(9)N(5))(2)](n), has been prepared by the solvothermal treatment of CuCl with 4-(2-allyl-2H-tetra-zol-5-yl)pyridine. The crystal structure shows that the title compound is a homometallic Cu(I)-olefin coordination polymer, in which the Cu(2)Cl(2) nodes are bridged by two olefin ligands. The asymmetric unit contains one-half of the monomer, the complete monomer having twofold rotation symmetry. The coordination environment of Cu(I) is slightly distorted tetra-he ...[more]

PMID: 21202785

Similar Datasets

catena-Poly[[di-?-bromido-dicopper(I)]bis-[?-?,?-4-(2-allyl-2H-tetra-zol-5-yl)pyridine]].

Project description:The title compound, [CuBr(C(9)H(9)N(5))](n), prepared by the solvothermal treatment of CuBr with 4-(2-allyl-2H-tetra-zol-5-yl)pyridine, is a new homometallic Cu(I)-olefin coordination polymer in which dinuclear Cu(2)Br(2) units are linked by the organic olefin ligand 4-(2-allyl-2H-tetra-zol-5-yl)pyridine, which acts as a bidentate ligand connecting two neighbouring Cu(2)Br(2) units through the pyridine N atom and the double bond of the allyl group. The coordination of Cu(I) is slightly distorted tetrahedral.

| S-EPMC2961675 | biostudies-literature

catena-Poly[[bromidocopper(I)]-?-?,?-3-(2-allyl-2H-tetra-zol-5-yl)pyridine].

Project description:The title compound, [CuBr(C(9)H(9)N(5))](n), has been prepared by the solvothermal treatment of CuBr with 3-(2-allyl-2H-tetra-zol-5-yl)pyridine. It is a new homometallic Cu(I) olefin coord-ination polymer in which the Cu(I) atoms are linked by the 3-(2-allyl-2H-tetra-zol-5-yl)pyridine ligands and bonded to one terminal Br atom each. The organic ligand acts as a bidentate ligand connecting two neighboring Cu centers through the N atom of the pyridine ring and the double bond of the allyl group. A three-dimensional structure is formed through weak Cu-Br [3.1579?(8)?Å], C-H?Br and C-H?N inter-actions.

| S-EPMC2961586 | biostudies-literature

catena-Poly[[chloridocopper(I)]-?-?,?-3-(2-allyl-2H-tetra-zol-5-yl)pyridine].

Project description:The title compound, [CuCl(C(9)H(9)N(5))](n), prepared by solvo-thermal synthesis, is a new homometallic Cu(I)-olefin coordination polymer in which the Cu(I) atoms are linked by the 3-(2-allyl-2H-tetra-zol-5-yl)pyridine ligands and are each bonded to one terminal Cl atom. The organic ligand acts as a bidentate ligand bridging two neighboring Cu centers through the bonds to the N atom of the pyridine ring and the double bond of the allyl group. Weak Cu?Cl [3.136?(8)?Å), C-H?Cl and C-H?N inter-actions connect the coordination polymers into a three-dimensional structure.

| S-EPMC2961697 | biostudies-literature

Poly[μ-chlorido-[μ(4)-5-(4-pyrid-yl)tetra-zol-ato]dicopper(I)].

Project description:The title three-dimensional coordination polymer, [Cu(2)Cl(C(6)H(4)N(5))](n), is the product of the hydro-thermal reaction of CuCl(2)·2H(2)O and 5-(4-pyrid-yl)-1H-tetra-zole (4-Hptz). The two independent Cu(I) ions are coordinated in distorted tetra-hedral and distorted trigonal coordination environments. In the unique 5-(4-pyrid-yl)-1H-tetra-zolate ligand, the dihedral angle between the pyridine and tetra-zole rings is 17.3 (2)°.

| S-EPMC2969065 | biostudies-literature

catena-Poly[potassium-di-?-aqua-?-4-(5-tetra-zolio)pyridine].

Project description:The title compound, [K(C(6)H(4)N(5))(H(2)O)(2)](n), was synthesized by hydro-thermal reaction of KOH with 4-(5-tetra-zolio)pyridine. The K atom has a distorted octa-hedral coordination environment and is coordinated by two axial N atoms from the organic ligand and by four water mol-ecules in the equatorial plane. The mol-ecules as a whole are located on crystallographic mirror planes; the K atom is also located on an inversion center. Both the water mol-ecules and the organic ligands act as bridges to link symmetrically the adjacent K atoms into polymeric chains parallel to the c axis. O-H?N hydrogen bonds involving the water O atoms and aromatic ?-? inter-actions [centroid-centroid distance 3.80?(2)?Å] between the pyridine and tetra-zole rings build up an infinite three-dimensional network.

| S-EPMC2969650 | biostudies-literature

catena-Poly[bis(1,3-benzo-thia-zol-3-ium) [[di-chlorido-anti-monate(III)]-di-μ-chlorido-μ-oxido-[chlorido-anti-monate(III)]-μ-chlorido]].

Project description:The title compound, {(C7H6NS)2[Sb2Cl6O]} n , contains two benzo-thia-zolidium cations and one tri-μ-chlorido-tri-chlorido-μ-oxido-di-anti-monate(III) anion. The structure of the inorganic cation may be described as as being built up from two polyhedra, i.e. a square-pyramidal SbCl4O and a distorted octa-hedral SbOCl5 unit, sharing a common face (comprising the O atom and two Cl atoms). The two benzo-thia-zole cations are quasi-planar and subtend a dihedral angle of 19.93 (5)°. The crystal packing can be described by alternating (100) layers and [001] chains of the organic cations and inorganic anions connected through an extensive three-dimensional network of N-H⋯Cl, C-H⋯O and C-H⋯Cl hydrogen bonds. This is consolidated by slipped π-π stacking, with centroid-to-centroid distances between the benzo-thia-zole rings of 3.7111 (18)-3.8452 (16) Å. These inter-actions link the mol-ecules within the layers and also link the layers together and reinforce the cohesion of the ionic structure.

| S-EPMC4770971 | biostudies-literature

catena-Poly[(dichloridocadmium)-di-?-chlorido-[bis-(morpholinium-?O)cadmium]-di-?-chlorido].

Project description:In the title compound, [Cd(2)Cl(6)(C(4)H(10)NO)(2)](n), the coordination geometry of each Cd(II) ion is distorted octa-hedral, but with quite different coordination environments. One Cd(II) atom is coordinated by four Cl atoms and two O atoms from two morpholinium ligands, while the other is coordinated by six Cl atoms. Adjacent Cd(II) atoms are inter-connected alternately by paired chloride bridges, generating a chain parallel to the a axis. Inter-chain N-H?Cl inter-actions form a two-dimensional network.

| S-EPMC3212201 | biostudies-literature

Crystal structure of catena-poly[N,N,N',N'-tetra-methyl-guanidinium [(chlorido-cadmate)-di-μ-chlorido]].

Project description:In the structure of the title salt, {(C5H14N3)[CdCl3]} n , the Cd(II) atom of the complex anion is five-coordinated by one terminal and four bridging Cl atoms. The corresponding coordination polyhedron is a distorted trigonal bipyramid, with Cd-Cl distances in the range 2.4829 (4)-2.6402 (4) Å. The bipyramids are condensed into a polyanionic zigzag chain extending parallel to [101]. The tetra-methyl-guanidinium cations are situated between the polyanionic chains and are linked to them through N-H⋯Cl hydrogen bonds, forming a layered network parallel to (010).

| S-EPMC4704744 | biostudies-literature

Crystal structure of catena-poly[1,3-di-benzyl-benzimidazolium [[chlorido-mercurate(II)]-di-?-chlorido]].

Project description:The asymmetric unit of the polymeric title compound, {(C21H19N2)[HgCl3]} n , comprises one-half of the cationic mol-ecule, the other half being generated by application of twofold rotation symmetry, one Hg and two Cl atoms. The Hg(II) atom, lying on a twofold rotation axis, exhibits a distorted triangular coordination environment and is surrounded by three Cl atoms with Hg-Cl distances in the range 2.359?(2)-2.4754?(13)?Å. Two additional longer distances [Hg?Cl = 3.104?(14)?Å] lead to the formation of polymeric [HgCl1/1Cl4/2](-) chains extending along [001]. The crystal packing can be described by cationic layers alternating parallel to (-110) with the anionic chains located between the layers. The packing is consolidated by ?-? stacking inter-actions between the benzene rings of the central benzimidazole entities, with centroid-to-centroid distances of 3.643?(3)?Å.

| S-EPMC4719861 | biostudies-literature

catena-Poly[heptyl-enedi-ammonium [[tetra-chloridobismuthate(III)]-?-chlorido]].

Project description:The title organic-inorganic hybrid compound, {(C7H20N2)[BiCl5]} n , consists of distorted corner-joined [BiCl6] octa-hedra forming zigzag polymeric anionic chains parallel to [001], separated by columns of heptyl-enedi-ammonium cations. The asymmetric unit contains two crystallographically independent bis-muth metal atoms, one of which lies on an inversion centre and the other on a twofold axis. In the crystal, the polymeric chains and cations are linked by N-H?Cl hydrogen bonds, forming undulating layers parallel to (110).

| S-EPMC3793680 | biostudies-literature

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