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Crystal structure of fac-tricarbon-yl(quinoline-2-carboxyl-ato-κ(2) N,O)(tri-phenyl-arsane-κAs)rhenium(I).

ABSTRACT: In the title compound, [Re(C10H6NO2)(CO)3{As(C6H5)3}], the coordination environment of Re(I) is that of a distorted octa-hedron. Three coordination sites are occupied by three carbonyl groups in a facial arrangement and the remaining three sites by tri-phenyl-arsane and deprotonated quinaldic acid in As-mono- and N,O-bidentate fashions, respectively. In the crystal, the complexes are linked through weak C-H⋯O hydrogen bonds, forming a three-dimensional network. It worth noting that, as far as we know, this complex is the first Re(I) tri-phenyl-arsane tricarbonyl compound to be reported.

SUBMITTER: Triantis C

PROVIDER: S-EPMC4770954 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Crystal structure of fac-tricarbon-yl(cyclo-hexyl isocyanide-?C)(quinoline-2-carboxyl-ato-?(2) N,O)rhenium(I).

Project description:In the title compound, [Re(C10H6NO2)(C7H11N)(CO)3], the Re(I) atom is coordinated by three carbonyl ligands in a facial arrangement and by the N, O and C atoms from a chelating quinaldate anion and a monodentate isocyanide ligand, respectively. The resultant C4NO coordination sphere is distorted octa-hedral. A lengthening of the axial Re-CO bond trans to the isocyanide ligand is indicative of the trans effect. Individual complexes are stacked into rods parallel to [001] through displaced ?-? inter-actions. Weak C-H?O hydrogen-bonding inter-actions between the rods lead to the formation of layers parallel to (010). These layers are stacked along [010] by C-H?H-C van der Waals contacts.

| S-EPMC4778812 | biostudies-other

Aqua-tricarbon-yl(4-carboxy-pyridine-2-carboxyl-ato-?N,O)rhenium(I).

Project description:There are two mol-ecules with similar bond dimensions in the asymmetric unit of the title complex, [Re(C(7)H(4)NO(4))(CO)(3)(H(2)O)]. The metal centre is coordinated facially by three carbonyl groups, is chelated by a 4-carboxy-pyridine-2-carboxyl-ate ligand and is also coordinated by a water mol-ecule. O-H?O hydrogen bonds give rise to a three-dimensional network.

| S-EPMC2959348 | biostudies-literature

fac-Tricarbon-yl(pyridine-?N)(1,1,1-trifluoro-acetyl-acetonato-?O,O')rhenium(I).

Project description:In the title compound, [Re(C(5)H(4)F(3)O(2))(C(5)H(5)N)(CO)(3)], the Re(I) atom is six-coordinated owing to bonding by three carbonyl ligands arranged in a fac configuration, two O atoms from the bidentate 1,1,1-trifluoro-acetyl-acetonate ligand and an N atom from a pyridine ligand. In the crystal, the mol-ecules pack in layers, diagonally, in a head-to-tail fashion across the ab plane. These layers are stabilsed by inter-molecular C-H?O and C-H?F hydrogen bonds.

| S-EPMC3247548 | biostudies-literature

Bis(?-2-phenyl-quinoline-4-carboxyl-ato)-?O,O':O;?O:O,O'-bis-[(2,2'-bipyridine-?N,N')(2-phenyl-quinoline-4-carboxyl-ato-?O,O')cadmium(II)].

Project description:The neutral binuclear title complex, [Cd(2)(C(16)H(10)NO(2))(4)(C(10)H(8)N(2))(2)], is centrosymmetric, with the inversion center generating the central (?-O)(2)Cd(2) bridge. The Cd(II) ion is in a strongly distorted CdN(2)O(5) penta-gonal-bipyramidal geometry, defined by two N atoms from one 2,2'-bipyridine ligand and five O atoms from three 2-phenyl-quinoline-4-carboxyl-ate ligands, one monodentate, two bidentate. Weak inter-molecular ?-? inter-actions [centroid-centroid distance = 3.712?(3)?Å] help to establish the packing of the structure.

| S-EPMC3050170 | biostudies-literature

Crystal structure of bromido-fac-tricarbon-yl[5-phenyl-3-(pyridin-2-yl)-1H-1,2,4-triazole-?(2) N,N']rhenium(I).

Project description:In the title compound, [ReBr(C13H10N4)(CO)3], the Re(I) atom has a distorted octa-hedral coordination environment. Two N atoms of the 5-phenyl-3-(pyridin-2-yl)-1H-1,2,4-triazole ligand and two of the three carbonyl groups occupy the equatorial plane of the complex, with the third carbonyl ligand and the bromide ligand in the axial positions. The three carbonyl ligands are arranged in a fac configuration around the Re(I) atom. Mutual N-H?Br hydrogen bonds arrange mol-ecules into centrosymmetric dimers. Additional stabilization within the crystal structure is provided by C-H?O and C-H?Br hydrogen bonds, as well as by slipped ?-? stacking inter-actions [centroid-to-centroid distance = 3.785?(5)?Å], defining a three-dimensional network.

| S-EPMC4257395 | biostudies-literature

Bis(?-2-phenyl-quinoline-4-carboxyl-ato)bis-[aqua-(1,10-phenanthroline)(2-phenyl-quinoline-4-carboxyl-ato)manganese(II)] dihydrate.

Project description:In the centrosymmetric dinuclear title complex, [Mn(2)(C(16)H(10)NO(2))(4)(C(12)H(8)N(2))(2)(H(2)O)(2)]·2H(2)O, the Mn(II) cation is in a distorted octa-hedral coordination geometry defined by two N atoms from a 1,10-phenanthroline ligand, one water O atom and three O atoms from three 2-phenyl-quinoline-4-carboxyl-ate anions. A pair of 2-phenyl-quinoline-4-carboxyl-ate anions bridge two Mn cations, forming the dinuclear mol-ecule. An intra-moleculr O-H?O hydrogen bond occurs. Inter-molecular O-H?O and O-H?N hydrogen bonds are present in the crystal structure.

| S-EPMC3201393 | biostudies-other

Poly[bis-(?-hemihydrogen 2-phenyl-quinoline-4-carboxyl-ato-?N,O)silver(I)].

Project description:In the title compound, [Ag(C(16)H(10.5)NO(2))(2)], the Ag(I) cation (site symmetry 2) is coordinated by two N atoms in a near-linear AgN(2) arrangement. Two carboxyl-ate O atoms from two additional 2-phenyl-quinoline-4-carboxyl-ate ligands form long Ag-O bonds [2.6585?(17)?Å], resulting in a distorted square-planar arrangement. The bridging ligands result in infinite corrugated sheets propagating in (010). An O-H?O hydrogen bond, disordered about a twofold axis, completes the structure.

| S-EPMC2968213 | biostudies-literature

fac-Tris(pyridine-2-carboxyl-ato-?N,O)cobalt(III).

Project description:In the title compound, [Co(C(6)H(4)NO(2))(3)], the Co(III) ion lies on a threefold rotation axis and is in a distorted octa-hedral environment defined by three N and three O donor atoms from three fac-disposed pyridine-2-carboxyl-ate ligands. The ligands are coordinated in a chelate fashion, forming three five-membered rings. In the crystal, translationally related complex molecules are organized into columns along [001] via C-H?O hydrogen bonds.

| S-EPMC3247521 | biostudies-literature

Poly[[penta-aqua-(?(4)-pyridine-2,4,6-tri-carboxyl-ato)(?(3)-pyridine-2,4,6-tri-carboxyl-ato)diterbium(III)] mono-hydrate].

Project description:The three-dimensional title coordination polymer, {[Tb(2)(C(8)H(2)NO(6))(2)(H(2)O)(5)]·H(2)O}(n), was hydro-thermally synthesized by reacting the corresponding rare-earth salt with pyridine-2,4,6-tricarb-oxy-lic acid (H(3)ptc). There are two independent Tb(III) atoms in the structure, one of which is nine-coordinated, forming a monocapped NO(8) square-anti-prism and the other is eight-coordinated exhibiting a 4,4-bicapped NO(7) trigonal-prismatic environment. The complex units are inter-connected through the ptc(3-) anions acting in different coordination modes, resulting in a three-dimensional coordin-ation polymer. The crystal structure features extensive O-H?O hydrogen bonds.

| S-EPMC3414173 | biostudies-literature

Poly[[penta-aqua-(?(4)-pyridine-2,4,6-tri-carboxyl-ato)(?(3)-pyridine-2,4,6-tri-carboxyl-ato)disamarium(III)] mono-hydrate].

Project description:The asymmetric unit of the title compound, {[Sm(2)(C(8)H(2)NO(6))(2)(H(2)O)(5)]·H(2)O}(n), contains two independent Sm(III) ions, two pyridine-2,4,6-tricarboxyl-ate (ptc) ligands, five aqua ligands and one lattice water mol-ecule. One Sm(III) ion is nine-coordinated by one N and five O atoms from the three ptc ligands and three aqua ligands in a distorted monocapped square antiprismatic geometry, and the other is eight-coordinated by one N and five O atoms from three ptc ligands and two aqua ligands in a 4,4'-bicapped trigonal anti-prismatic geometry. The ptc ligands brigde the Sm(III) ions into a three-dimensional polymeric framework. Extensive O-H?O hydrogen bonding is observed in the crystal structure.

| S-EPMC3297243 | biostudies-literature

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