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Synthesis, crystal structure and thermal properties of dibromidobis(2-methylpyridine N-oxide-κO)cobalt(II)

ABSTRACT:

SUBMITTER: Nather C

PROVIDER: S-EPMC10848989 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature

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Synthesis, crystal structure and reactivity of bis-(μ-2-methyl-pyridine N-oxide-κ2O:O)bis-[di-bromido-(2-methyl-pyridine N-oxide-κO)cobalt(II)] butanol monosolvate.

Project description:Reaction of CoBr2 with 2-methyl-pyridine N-oxide in n-butanol leads to the formation of the title compound, [CoBr2]2(2-methyl-pyridine N-oxide)4·n-butanol or [Co2Br4(C6H7NO)4]·C4H10O. The asymmetric unit of the title compound consists of one CoII cation as well as two bromide anions and two 2-methyl-pyridine N-oxide coligands in general positions and one n-butanol mol-ecule that is disordered around a center of inversion. The CoII cations are fivefold coordinated by two bromide anions and one terminal as well as two bridging 2-methyl-pyridine N-oxide and linked by two symmetry-related μ-1,1(O,O) 2-methyl-pyridine N-oxide coligands into dinuclear units that are located on centers of inversion. In the crystal structure, the dinuclear units are also connected via pairs of C-H⋯Br hydrogen bonds into chains that elongate in the b-axis direction. The n-butanol mol-ecules are located between the chains and are linked via O-H⋯Br hydrogen bonds each to one chain. Powder X-ray diffraction (PXRD) measurements reveal that a pure phase has been obtained. Measurements using thermogravimetry and differential thermoanalysis shows one mass loss up to 523 K, in which the n-butanol mol-ecules are removed. PXRD measurements of the residue obtained after n-butanol removal shows that a completely different crystalline phase has been obtained and IR investigations indicate significant structural changes in the Co coordination.

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Crystal structure of bis-(3,5-di-methyl-pyridine-κN)bis-(methanol-κO)bis-(thio-cyanato-κN)cobalt(II).

Project description:The asymmetric unit of the title complex, [Co(NCS)2(C7H9N)2(CH3OH)2], comprises of one CoII cation located on a centre of inversion, one thio-cyanate ligand, one methanol ligand and one 3,5-di-methyl-pyridine ligand. The CoII cation is octa-hedrally coordinated by two terminal N-bonding thio-cyanate anions, two methanol mol-ecules and two 3,5-di-methyl-pyridine ligands into a discrete complex. The complex mol-ecules are linked by inter-molecular O-H⋯S hydrogen bonding into chains that elongate in the direction parallel to the b axis.

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cis-Bromido(methyl-amine)-bis-(propane-1,3-di-amine)-cobalt(III) dibromide.

Project description:In the title compound, [CoBr(CH5N)(C3H10N2)2]Br2, the cobalt(III) ion has a distorted octa-hedral coordination environment and is surrounded by four N atoms in the equatorial plane, with an additional N atom and the Br atom occupying the axial positions. In the crystal, the complex cation and the two counter anions are linked via N-H⋯Br and C-H⋯Br hydrogen bonds, forming a three-dimensional network.

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Project description:Cobalt(II) nitrate hexa-hydrate and sodium dicyanamide self-assembled in dimethyl-formamide (DMF) and 4-methyl-pyridine solutions to form the title compound, [Co(C(2)N(3))(2)(C(6)H(7)N)(2)](n). The Co(2+) ion lies on an inversion center and adopts an octa-hedral coordination geometry in which four N atoms from four different dicyanamide ligands lie in the equatorial plane and two 4-methyl-pyridine N atoms occupy the axial positions. The Co(II) atoms are connected by two bridging dicyanamide ligands, resulting in a chain parallel to the c axis. The chains are connected into a three-dimensional network by C-H⋯N hydrogen bonds.

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Crystal structures of di-μ-bromido-bis{di-bromido-[η5-2-(di-methyl-amino)-inden-yl]zirconium(IV)} and di-bromido-bis-[η5-2-(di-methyl-amino)-inden-yl]zirconium(IV).

Project description:In the title compounds, [Zr2Br6(C11H12N)2], (I) and [ZrBr2(C11H12N)2], (II), the positions of the η5-binding 2-di-methyl-amino-indenyl units are fixed by intra-molecular C-H⋯Br inter-actions involving aromatic or di-methyl-amino H atoms. The binuclear mol-ecule of (I) is located on a general position, while the mononuclear mol-ecule of (II) is situated on a twofold rotation axis. Both ZrIV atoms in (I) are ligated by one cyclo-penta-dienyl (CP) ring and four Br ligands (two bridging, two terminal), while in (II) the ZrIV atom is ligated by two CP rings and two terminal Br ligands. The crystal structures of both (I) and (II) comprise of strands of π-π- and N-π-bonded mol-ecules, which in turn are linked by C-H⋯Br inter-actions.

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catena-Poly[di-μ3-bromido-hexa-μ2-bromido-dibromidobis(O-methyl pyridine-2-carboximidate-κ(2) N,N')penta-mercury(II)].

Project description:The title compound, [Hg5Br10(C7H8N2O)2] n , contains two μ3-bridging Br atoms, six μ2-bridging Br atoms and two terminal Br atoms. One Hg(II) atom, lying on an inversion center, adopts a distorted octa-hedral geometry defined by six Br atoms. Two Hg(II) atoms adopt a distorted square-pyramidal geometry by five Br atoms and the other two Hg(II) atoms have a distorted tetra-hedral geometry by two N atoms from a chelating O-methyl pyridine-2-carboximidate ligand and two Br atoms. The Br atoms link the Hg(II) atoms into a ribbon structure along [100].

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μ-Methyl-ene-bis-[di-bromido(diethyl ether-κO)aluminium(III)]: crystal structure and chemical exchange in solution.

Project description:In the title compound, [Al2Br4(CH2)(C4H10O)2], the mol-ecule lies on a crystallographic twofold axis passing through the bridging C atom. Each AlIII atom is four-coordinate, being bonded to two bromide ions, bridging the CH2 group as well as the oxygen atom of a diethyl ether ligand in a slightly distorted tetra-hedral arrangement with angles ranging from 101.52 (8) to 116.44 (5)°. The Al-CH2-Al angle, 118.4 (2)°, is the smallest observed for a structure where this moiety is not part of a ring. In the crystal, weak C-H⋯Br inter-actions, characterized as R 2 2(12) rings, link the mol-ecules into ribbons in the [101] direction. The title compound is monomeric and coordinatively saturated in the solid state, as each aluminum is four-coordinate, but in solution the ether mol-ecules from either or both Al atoms can dissociate, and would be expected to rapidly exchange, and this is supported by NMR data.

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Crystal structure of di-bromido-bis-(1,3-dibenzyl-1,3-diazinan-2-one-κO)cobalt(II).

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