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Synthesis, crystal structure and magnetic properties of poly[[diaqua{μ₆-2-[bis-(carboxyl-atometh-yl)amino]-terephthalato}-dicobalt(II)] 1.6-hydrate].

ABSTRACT: The asymmetric unit of the polymeric title compound {[Co₂(C₁₂H₇NO₈)(H₂O)₂]·1.6H₂O} _n comprises two Co^II ions, which are coordinated by fully deprotonated 2-aminodi-acetic terephthalic acid (adtp^4-) and terminal water mol-ecules in distorted octa-hedral N₁O₅ and O₆ coordination environments. The title compound features tetra-nuclear Co^II units bridged by κ ³ O:O:O'- and κ ³ O:O,O'-carboxyl-ate groups, which are joined into ribbons via syn-anti carboxyl-ate bridges. The parallel adtp^4- ligands with an alternately reversed arrangement further link adjacent Co^II ribbons into (010) layers, which are assembled into a three-dimensional supra-molecular network via inter-molecular hydrogen bonds. The disordered water solvent mol-ecules are situated in channels parallel to [100]. Magnetic measurements and analyses reveal that the title compound displays anti-ferromagnetic behaviour. The purity of the title compound was characterized by X-ray powder diffraction.

SUBMITTER: Ma J

PROVIDER: S-EPMC8423006 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Synthesis and crystal structure of <i>catena</i>-poly[[hexa-aqua{μ<sub>3</sub>-2-[bis-(carboxyl-atometh-yl)amino]-terephthalato}dicobalt(II)] penta-hydrate] containing water tapes and penta-mers.

Project description:The title coordination polymer, {[Co2(C12H7NO8)(H2O)6]·5H2O} n , was crystallized at room temperature from an aqueous solution of 2-aminodi-acetic terephthalic acid (H4adtp) and cobalt(II) nitrate. The asymmetric unit consists of one adtp4- ligand, one and two half CoII ions, six water ligands coordinated to CoII ions and five uncoordinated water mol-ecules. Two of the cobalt cations lie on centres of inversion and are coordinated in octa-hedral O2(OH2)4 environments, whereas the other adopts a slightly distorted octa-hedral NO3(OH2)2 environment. The crystal structure contains parallel stacked, one-dimensional zigzag chains, {[Co2(C12H7NO8)(H2O)6]} n , which assemble into a three-dimensional supra-molecular architecture via networks of hydrogen bonds involving the coordinated and free water mol-ecules. One-dimensional 'water tapes' are formed, containing alternating six-membered and twelve-membered rings of water mol-ecules, together with water penta-mers, in which a central uncoordinated water mol-ecule is hydrogen bonded to two coordinated and two free water mol-ecules in a tetra-hedral arrangement.

| S-EPMC8423001 | biostudies-literature

Poly[diaqua-μ(2)-oxalato-di-μ(4)-terephthalato-diytterbium(III)].

Project description:The crystal structure of the title complex, [Yb(2)(C(8)H(4)O(4))(2)(C(2)O(4))(H(2)O)(2)](n), features an extended three-dimensional framework made up of Yb(3+) ions coordinated by terephthalate ligands, oxalate ligands and water mol-ecules. The Yb(3+) ion has a distorted square-anti-prismatic coordination formed by one aqua ligand, two O atoms from an oxalate ligand and five O atoms belonging to four terephthalate anions. Two symmetry-independent terephthalate anions, as well as the oxalate anion, occupy special positions on inversion centers. The water molecule participates in O-H⋯O hydrogen bonding with both terephthalate anions.

| S-EPMC3008045 | biostudies-literature

Poly[[diaqua-(μ(4)-l-tartrato)(μ(2)-l-tartrato)dizinc(II)] tetra-hydrate].

Project description:In the title compound, {[Zn(C(4)H(4)O(6))(H(2)O)]·2H(2)O}(n), the l-tartrate ligands adopt μ(4)- and μ(2)-coordination modes. The Zn(II) atom adopts an octa-hedral geometry and is chelated by two kinds of l-tartrate ligands through the hydr-oxy and carboxyl-ate groups and coordinated by one unchelating carboxyl-ate O atom and one water mol-ecule. In the crystal, the l-tartrate ligands link the Zn(II) atoms, forming a two-dimensional coordination layer; these layers are futher linked into a three-dimensional supra-molecular network by O-H⋯O hydrogen bonds between the two-dimensional coordin-ation layers and the uncoordinated water mol-ecules. The latter are equally disordered over two positions.

| S-EPMC2983975 | biostudies-literature

catena-Poly[[[bis-(3-amino-pyrazine-2-carboxyl-ato)triaqua-praseodymium(III)]-μ-3-amino-pyrazine-2-carboxyl-ato-[(3-amino-pyrazine-2-carboxyl-ato)diaqua-formatopraseodymium(III)]-μ-3-amino-pyrazine-2-carboxyl-ato] hexa-hydrate].

Project description:The asymmetric unit of the polymeric title compound, {[Pr(2)(C(5)H(4)N(3)O(2))(5)(CHO(2))(H(2)O)(5)]·6H(2)O}(n), has two independent Pr(III) atoms; one is coordinated by two water mol-ecules and the other by three water mol-ecules. The first is N,O-chelated by three 3-amino-pyrazine-2-carboxyl-ate ions, whereas the second is chelated by two carboxyl-ate ions; both exist in a monocapped square-anti-prismatic geometry. The polymeric chains that run along the a axis inter-act with the lattice water mol-ecules, generating a three-dimensional hydrogen-bonded network. The formate ion is disordered over two positions with respect to the non-coordinated atoms in a 1:1 ratio.

| S-EPMC3200950 | biostudies-literature

Poly[[octaaqua-?4-(benzene-1,2,4,5-tetra-carboxyl-ato)-dicobalt(II)] octa-hydrate].

Project description:The title polymeric coordination compound, {[Co2(C10H2O8)(H2O)8]·8H2O} n , was obtained by slow diffusion of a dilute aqueous solution of CoCl2 and the sodium salt of benzene-1,2,4,5-tetracarboxylic acid (H4btec) through an agar-agar gel bridge in a U-shaped tube. The two independent Co(2+) ions are each situated on an inversion centre and are coordinated in a slightly distorted octa-hedral geometry by four water O atoms and two carboxyl-ate O atoms from two btec(4-) ligands (-1> symmetry), forming a layer parallel to (11-1). This layer can be described as a mol-ecular two-dimensional square grid with the benzene rings at the nodes and the Co(II) atoms connecting the nodes. O-H?O hydrogen-bonding interactions involving the coordinating water molecules, the carboxylate O atoms and lattice water molecules lead to the formation of a three-dimensional network.

| S-EPMC3885008 | biostudies-other

catena-Poly[[[diaqua-thulium(III)]-μ-6-carboxy-nicotinato-μ-pyridine-2,5-di-carboxyl-ato] dihydrate].

Project description:The title compound, {[Tm(C(7)H(3)NO(4))(C(7)H(4)NO(4))(H(2)O)(2)]·2H(2)O}(n), is isotypic with the analogous Tb(III) compound [Li et al. (2009 ▶). Acta Cryst. E65, m410]. All interatomic distances and angles and the hydrogen-bond geometries are very similar for the two structures. The refined Flack parameter of 0.49 (2) suggests inversion twinning.

| S-EPMC2968913 | biostudies-literature

catena-Poly[[[diaqua-terbium(III)]-μ-6-carboxy-nicotinato-μ-pyridine-2,5-di-carboxyl-ato] dihydrate].

Project description:The title compound, {[Tb(C(7)H(3)NO(4))(C(7)H(4)NO(4))(H(2)O)(2)]·2H(2)O}(n), is isotypic with the analogous Tm(III) compound [Li, Zhang, Wang & Bai (2009). Acta Cryst. E65, m411]. The Tb(III) atom is octa-coordinated by two water mol-ecules and by four carboxyl-ate O atoms and two pyridyl N atoms from two pyridine-2,5-dicarboxyl-ate (2,5-pydc) and two 6-carboxy-nicotinate (2,5-Hpydc) ligands. The 2,5-pydc and 2,5-Hpydc ligands bridge Tb(III) atoms, generating helical coordination polymers along [001]. An extensive network of O-H⋯O hydrogen bonds is formed between the coordination polymers and the uncoordinated water mol-ecules. The refined Flack parameter of 0.54 (2) suggests inversion twinning.

| S-EPMC2968984 | biostudies-literature

Poly[diaqua-?(2)-oxalato-di-?(4)-terephthalato-dilutetium(III)].

Project description:In the title compound, [Lu(2)(C(8)H(4)O(4))(2)(C(2)O(4))(H(2)O)(2)](n), the Lu(3+) cations are each coordinated by eight O atoms of four terephthalate anions, one oxalate anion and one aqua ligand to complete a distorted square-anti-prismatic geometry. They are bridged by the terephthalate ligands, generating a three-dimensional framework, which is further stabilized by the oxalate ligands. The terephthalate ions and oxalate ions are all located on centers of inversion.

| S-EPMC2970178 | biostudies-literature

Poly[[diaqua[μ(5)-(R,S)-2-({2-[(1,2-di-carboxyl-atoeth-yl)amino]-eth-yl}amino)-butane-dioato]cobaltate(III)sodium] di-hydrate].

Project description:In the asymmetric unit of the title coordination polymer, {[CoNa(C(10)H(12)N(2)O(8))(H(2)O)(2)]·2H(2)O}(n), the Co(II) ion is coord-inated in a distorted octa-hedral environment, defined by two N atoms and four carboxyl-ate O atoms. Two Co(II) ions and two 2-({2-[(1,2-dicarboxyl-atoeth-yl)amino]-eth-yl}amino)-butane-dio-ate (EDDS) ligands form a dimeric complex dianion [Co(2)(EDDS)(2)]. These dimeric units are connected via Na(+) ions, forming a three-dimensional polymeric structure. In the crystal, the ligand N-H groups and the coordinated and solvent water mol-ecules are involved in inter-molecular N-H⋯O and O-H⋯O hydrogen bonding, reinforcing the three-dimensional polymeric structure.

| S-EPMC3246970 | biostudies-literature

Poly[[diaqua-tris(?2-4,4'-bi-pyridine)-bis[?2-2-(carb-oxylato-methyl-sulfan-yl)nicotinato]dicobalt(II)] 1.3-hydrate].

Project description:The title complex, [Co2(C8H5NO4S)2(C10H8N2)3(H2O)2]·1.3H2O, was synthesized under hydro-thermal conditions. The Co(II) ion is six-coordinated in a slightly distorted octa-hedral environment resulting from two carboxyl-ate O atoms of two 2-carb-oxy-methyl-sulfanyl nicotinate (2-CMSN(2-)) anions, one water mol-ecule and three N atoms of three 4,4'-bi-pyridine ligands, with one 4,4'-bi-pyridine ligand situated on a centre of inversion. Two neighboring Co(II) ions are linked by two anions, giving a dinuclear [Co2(2-CMSN)2] subunit with a Co?Co separation of 6.8600?(3)?Å. The dinuclear subunits are joined by bridging 4,4'-bi-pyridine linkers, generating a three-dimensional network structure. Disordered water mol-ecules are situated in the free space of this network. O-H?O hydrogen bonding within and between the subunits enhances the stability of the structure.

| S-EPMC3772411 | biostudies-literature