Search results for "COBALT"

showing 10 items of 1098 documents

Metal complexes of the carbonic anhydrase inhibitor methazolamide (Hmacm). Crystal structure of the Zn(macm)2 (NH3)2. Anticonvulsant properties of th…

1995

Complexes of Co(II), Cu(II), and Zn(II) with deprotonated methazolamide and ammonia are synthesized and characterized. The complex Zn(macm)2(NH3)2 crystallizes in the monoclinic C2/c space group with a = 13.468(1), b = 6.759(1), c = 23.014(2) A, beta = 90.27(1), and Z = 4. The structure was refined to R = 0.049 (Rw = 0.053). The Zn(II) ion is coordinated to two deprotonated sulfonamido nitrogen atoms of the macm- ligand and two nitrogen atoms of the ammonia ligands in a distorted tetrahedron. The Zn(macm)2(NH3)2 complex is shown to be a simple model for the methazolamide inhibition of CA. EHMO calculations applied to fractional coordinates of the Zn(macm)2(NH3)2 complex indicate that the at…

Spectrophotometry InfraredCations DivalentInorganic chemistryMethazolamidechemistry.chemical_elementCrystal structureZincCrystallography X-RayBiochemistryInorganic ChemistryMetalDeprotonationmedicineAnimalsMethazolamideHOMO/LUMOMolecular StructureChemistryLigandElectron Spin Resonance SpectroscopyCobaltZincCrystallographyvisual_artvisual_art.visual_art_mediumAnticonvulsantsCoppermedicine.drugMonoclinic crystal systemJournal of Inorganic Biochemistry
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Guest-dependent single-ion magnet behaviour in a cobalt(ii) metal-organic framework.

2015

Single-ion magnets (SIMs) are the smallest possible magnetic devices for potential applications in quantum computing and high-density information storage. Both, their addressing in surfaces and their organization in metal-organic frameworks (MOFs) are thus current challenges in molecular chemistry. Here we report a two-dimensional 2D MOF with a square grid topology built from cobalt(ii) SIMs as nodes and long rod-like aromatic bipyridine ligands as linkers, and exhibiting large square channels capable to host a large number of different guest molecules. The organization of the cobalt(ii) nodes in the square layers improves the magnetic properties by minimizing the intermolecular interaction…

Square tiling010405 organic chemistryIntermolecular forcechemistry.chemical_elementNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesCrystallographyBipyridinechemistry.chemical_compoundchemistryMagnetMoleculeMetal-organic frameworkCobaltTopology (chemistry)Chemical science
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Effect of Cyanato, Azido, Carboxylato, and Carbonato Ligands on the Formation of Cobalt(II) Polyoxometalates: Characterization, Magnetic, and Electro…

2007

Five Co(II) silicotungstate complexes are reported. The centrosymmetric heptanuclear compound K(20)[{(B-beta-SiW(9)O(33)(OH))(beta-SiW(8)O(29)(OH)(2))Co(3)(H(2)O)}(2)Co(H(2)O)(2)]47 H(2)O (1) consists of two {(B-beta-SiW(9)O(33)(OH))(beta-SiW(8)O(29)(OH)(2))Co(3)(H(2)O)} units connected by a {CoO(4)(H(2)O)(2)} group. In the chiral species K(7)[Co(1.5)(H(2)O)(7))][(gamma-SiW(10)O(36))(beta-SiW(8)O(30)(OH))Co(4)(OH)(H(2)O)(7)]36 H(2)O (2), a {gamma-SiW(10)O(36)} and a {beta-SiW(8)O(30)(OH)} unit enclose a mononuclear {CoO(4)(H(2)O)(2)} group and a {Co(3)O(7)(OH)(H(2)O)(5)} fragment. The two trinuclear Co(II) clusters present in 1 enclose a mu(4)-O atom, while in 2 a mu(3)-OH bridging group co…

Stereochemistry010405 organic chemistryOrganic ChemistryCenter (category theory)chemistry.chemical_elementGeneral ChemistryGeneral Medicine[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysis0104 chemical sciencesRedox ActivityParamagnetismCrystallographychemistryElectronic effectCompound K[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]CobaltComputingMilieux_MISCELLANEOUS
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Preferential azido bridging regulating the structural aspects in cobalt(III) and copper(II)–Schiff base complexes: Syntheses, magnetostructural corre…

2011

International audience; A tridentate NNO donor Schiff base ligand [(1Z,3E)-3-((pyridin-2-yl)methylimino)-1-phenylbut-1-en-1-ol = LH] in presence of azide ions coordinates with cobalt(II) and copper(II) ions giving rise to three new coordination complexes [Co2(L)2(μ1,1-N3)2(N3)2] (1), [Cu2(L)2(μ1,3-N3)]·ClO4 (2) and [(μ1,1-N3)2Cu5(μ-OL)2(μ1,1-N3)4(μ1,1,1-N3)2]n (3). The complexes have been characterized by elemental analysis, FT-IR, UV–Vis spectral studies, and single crystal X-ray diffraction studies. These complexes demonstrate that under different synthetic conditions the azide ions and the Schiff base ligand (LH) show different coordination modes with cobalt(II) and copper(II) ions, givi…

Stereochemistry1chemistry.chemical_elementCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesPhysical and Theoretical Chemistrychemistry.chemical_classification1-Schiff base010405 organic chemistryAlkene3-Azide[CHIM.MATE]Chemical Sciences/Material chemistryCopper0104 chemical sciencesCrystallographyCuII Schiff basechemistryVTM Alkene oxidationCrystal structuresM = CoIIIAzideμ1Single crystalCobalt
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Iron(III), chromium(III) and cobalt(II) complexes with squarate: Synthesis, crystal structure and magnetic properties

2011

The preparation and variable temperature-magnetic investigation of three squarate-containing complexes of formula [Fe 2 (OH) 2 (C 4 O 4 ) 2 (H 2 O) 4 ]·2H 2 O ( 1 ) [Cr 2 (OH) 2 (C 4 O 4 ) 2 (H 2 O) 4 ]·2H 2 O ( 2 ) and [Co(C 4 O 4 )(H 2 O) 4 ] n ( 3 ) [H 2 C 4 O 4  = 3.4-dihydroxycyclobutene-1,2-dione (squaric acid)] together with the crystal structures of 1 and 3 are reported. Complex 1 contains discrete centrosymmetric [Fe 2 (OH) 2 (C 4 O 4 ) 2 (H 2 O) 4 ] diiron(II) units where the iron pairs are joined by a di-μ-hydroxo bridge and two squarate ligands acting as bridging groups through adjacent oxygen atoms. Two coordinated water molecules in cis position complete the octahedral environ…

StereochemistryChemistrychemistry.chemical_elementCrystal structureSquaric acidInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronIntramolecular forceMaterials ChemistryAntiferromagnetismMoleculePhysical and Theoretical ChemistryIsostructuralCobaltInorganica Chimica Acta
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A two-dimensional magnetic architecture with bridging polynitrile and 2,2′-bipyrimidine ligands

2004

cited By 7; International audience; A new polymeric, two-dimensional compound [Co2(bpym)(dcne) 4 (H2O)2] (1) (dcne = [(CN)2CC(O) OEt)]- = 2,2-dicyano-1-ethoxyethenolate anion and bpym = 2,2'-bipyrimidine) has been synthesized and characterized by X-ray crystallography. The structure is monoclinic space group P21/a and consists of two-dimensional networks of octahedrally coordinated Co(II) ions, bridged by bis-bidentate 2,2'-bipyrimidine and μ2-dcne anions. Magnetic measurements revealed a broad maximum in the xm vs T plot at 20 K which is characteristic of antiferromagnetic exchange between the high spin cobalt(II) centres. © EDP Sciences.

StereochemistryGeneral Physics and Astronomychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesNegative ionsCobalt complexesIonAntiferromagnetismTransition metal[CHIM]Chemical SciencesAntiferromagnetism2.2'-bipyrimidine010405 organic chemistryOrganic polymersSpace groupX ray crystallographyMagnetic measurementsMagnetic susceptibility3. Good health0104 chemical sciencesCrystallographychemistrySynthesis (chemical)CobaltMonoclinic crystal systemJournal de Physique IV (Proceedings)
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Single chain magnet behaviour in an enantiopure chiral cobalt(II)–copper(II) one-dimensional compound

2010

The self-assembly of an enantiomerically pure, chiral dianionic oxamatocopper(II) complex with cobalt(II) ions leads to neutral oxamato-bridged heterobimetallic chains that combine chirality and slow magnetic relaxation, providing thus the first example of ‘‘chiral single chain magnets (CSCMs). Ruiz Garcia, Rafael, Rafael.Ruiz@uv.es ; Lloret Pastor, Francisco, Francisco.Lloret@uv.es

StereochemistryHigh Energy Physics::LatticeUNESCO::QUÍMICAchemistry.chemical_elementSingle chainComputer Science::Computational Geometry010402 general chemistry01 natural sciences:QUÍMICA [UNESCO]CatalysisIonMagnetic RelaxationMaterials ChemistryMagnetic relaxation[CHIM.COOR]Chemical Sciences/Coordination chemistrySelf-assembly ; Dianionic oxamatocopper ; Cobalt ; Ions ; Magnetic RelaxationComputingMilieux_MISCELLANEOUSIons010405 organic chemistryUNESCO::QUÍMICA::Química inorgánicaHigh Energy Physics::PhenomenologyMetals and AlloysGeneral ChemistrySelf-assemblyCobalt:QUÍMICA::Química inorgánica [UNESCO]Copper3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyEnantiopure drugchemistryMagnetCeramics and CompositesDianionic oxamatocopperChirality (chemistry)Cobalt
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Six-coordinate CoIII and four-coordinate MII (M = Co, Zn) mixed-valence dimers supported by a deprotonated pyridine amide ligand: magnetism of a CoII…

2009

Using a pyridine amide ligand 4-methyl-2-{N-(2-pyridyl)carbamoyl}pyridine (HL), in its deprotonated form, binuclear mixed-valence homonuclear bimetallic complexes [CoIII,II2(L)3(X)]X·S [X = Cl (1); X = Br, S = CH3OH (2)] and heteronuclear bimetallic complex [CoIIIZnII(L)3(Cl)]Cl·CH3OH·5H2O (3) have been synthesized. Structural analysis revealed that trivalent cobalt is in distorted octahedral and bivalent cobalt/zinc is in distorted tetrahedral environment. Three L(−) ligands provide six-coordination by utilizing three pyridine amide units (pyridine N and amide N donor set) in a facial mode, which in turn places three 4-methylpyridine nitrogens to coordinate to another metal center, which c…

StereochemistryLigandDimerSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryCatalysischemistry.chemical_compoundCrystallographychemistryOctahedronHeteronuclear moleculeAmidePyridineMaterials ChemistryCobaltNew Journal of Chemistry
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Aerobic epoxidation of olefins catalysed by square-planar cobalt(III) complexes of bis-N,N′-disubstituted oxamides and related ligands

1997

The new square-planar nickel(II) complexes of o-phenylenebis(N′-methyloxamidate) and related ligands catalyse the aerobic epoxidation of olefins with co-oxidation of pivalaldehyde; the modulation of catalytic activity by substituents along this series of metal complexes points out the role of high-valent nicke(IV)-oxo species as the putative intermediate in these oxygen atom transfer reactions.

StereochemistryOrganic Chemistrychemistry.chemical_elementBiochemistryMedicinal chemistryCatalysisMetalNickelOxygen atomchemistryvisual_artDrug Discoveryvisual_art.visual_art_mediumCobaltTetrahedron Letters
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Synthesis and Physicochemical Characterization of Bis(macrocycles) Involving a Porphyrin and a meso ‐Substituted Corrole – X‐ray Crystal Structure of…

2005

A very efficient, simple synthesis of face-to-face porphyrin–corrole free-bases bearing substituents at the meso positions of the corrole ring is reported. Starting from the (porphyrin–aldehyde)zinc species 1Zn, porphyrin–corrole free-bases (3M, 3C) are obtained in two steps, in fairly good yields (40–43 %), compared to 11 steps for their corrole β-pyrrole-substituted counterparts. Moreover, the possibility to directly synthesize the free-base (porphyrin–corrole)cobalt complex (5M or 5C) allows for the further preparation of heterodimetallic derivatives. Crystals of the bis(pyridine) adduct of 5M have been grown; the molecular structure clearly shows that the two pyridine molecules are coor…

StereochemistryStackingFree basechemistry.chemical_elementCrystal structurePorphyrinAdductInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPyridineCorroleCobaltEuropean Journal of Inorganic Chemistry
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