Search results for "Ordination"

showing 10 items of 1367 documents

Malonate-based copper(II) coordination compounds: Ferromagnetic coupling controlled by dicarboxylates

2003

Studies on structural and magnetic properties of polynuclear transition metal complexes, aimed at understanding the structural and chemical factors governing electronic exchange coupling mediated by multiatom bridging ligands, are of continuing interest to design new molecular materials exhibiting unusual magnetic, optical and electrical properties, bound to their molecular nature. Looking at potentially flexible bridging ligands, the malonate group seems a suitable candidate. The occurrence of two carboxylate groups in the 1,3 positions allows this ligand to adopt simultaneously chelating bidentate and different carboxylato bridging modes (syn–syn, anti–anti and syn–anti trough one or two …

chemistry.chemical_classificationDenticityLigandStereochemistrychemistry.chemical_elementCopperCoordination complexInorganic ChemistryCrystallographychemistry.chemical_compoundMalonateFerromagnetismchemistryTransition metalMaterials ChemistryCarboxylatePhysical and Theoretical Chemistry
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Copper(II) complexes with 2,5-bis(2-pyridyl)pyrazine and oxalate and croconate: Synthesis, crystal structure and magnetic properties

2012

Abstract Two new copper(II) complexes of formula [Cu2(2,5-dpp)(C2O4)2(H2O)4] (1) and [Cu2(2,5-dpp)(C5O5)2(H2O)4]·3H2O (2) [2,5-dpp = 2,5-bis(2-pyridyl)pyrazine, C2O42− = oxalate and C5O52− = croconate (dianion of 4,5-dihydroxycyclopent-4-ene-1,2,3-trione)] have been prepared and their structures determined by X-ray crystallographic methods. Compounds 1 and 2 are dinuclear complexes where the 2,5-dpp molecule acts as a bis-bidentate bridge between the two copper(II) ions, the electroneutrality being achieved by the presence of bidentate oxalate (1) and croconate (2) ligands. Each copper(II) ion exhibits an elongated octahedral CuN2O4 environment with two nitrogen atoms from 2,5-dpp and two o…

chemistry.chemical_classificationDenticityPyrazineLigandInorganic chemistrychemistry.chemical_elementCrystal structureCopperOxalateCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
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Novel malonate-containing coordination compounds with ligands having N-And NO-donors: Synthesis, structures, and magnetic properties

2012

In our efforts to tune the structures of mixed-ligands malonate-containing coordination compounds, four copper(II) and two high-spin cobalt(II) complexes of formulas [Cu(mal)(H 2O)(dpo)] n (1), [Cu 2(mal) 2(H 2O) 2(dpp)] n · 7nH 2O (2), [Cu 2(mal) 2(H 2O) 2-(bpe)] n · 2nH 2O (3), {[Cu(mal) 2(H 2O) 2][Cu(dien)]} n · 4nH 2O (4)[Co 2(mal) 2(H 2O) 6(dpo)] ·2H 2O(5) and [Co(mal)(H 2O)(phen)] n · 2nH 2O (6) [H 2mal = malonic acid, dpo =4,4'-bipyridine-N,N'-dioxide, dpp = 2,3-bis(pyridyl)pyrazine, bpe =1,2-bis(4-pyridyl)ethylene, dien = diethylenetriamine and phen = 1,10-phenanthroline] have been synthesized and structurally characterized by X-ray diffraction on single crystals. Complexes 1, 2, 4,…

chemistry.chemical_classificationDenticityPyrazineLigandStereochemistryBridging ligandGeneral ChemistryMalonic acidCondensed Matter PhysicsCoordination complexchemistry.chemical_compoundMalonatechemistryDiethylenetriamineGeneral Materials ScienceCrystal Growth and Design
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Insertion of FeII complexes with Schiff base ligands derived from imidazole or pyridine into 3D bimetallic oxalate-based ferromagnets

2013

Abstract The syntheses, structures and magnetic properties of the compounds [FeII(imid2-trien)][MnII(CH3OH)CrIII(ox)3]2·(CH3OH)4(CH3CN)(H2O) (1), [FeII(tren(6-Me-py)3)][MnIICrIII(ox)3][MnII(CH3OH)0.58(H2O)0.42CrIII(ox)3]·(CH3OH)2(CH3CN)0.5(H2O)0.42 (2) and [FeII(tren(imid)3)]2[Mn2.5(CH3OH)3Cr3(ox)9]·(CH3OH)4.75·(H2O)4.25 (3) are reported. They are prepared by the insertion of FeII-Schiff base complexes derived from imidazole and pyridine into bimetallic oxalate networks. Different types of 3D oxalate networks are obtained for each templating cation. Thus, [FeII(imid2-trien)]2+ and [FeII(tren(6-Me-py)3)]2+ give rise to unusual 3D achiral bimetallic oxalate networks with heptacoordinated MnII…

chemistry.chemical_classificationDenticitySchiff base010405 organic chemistryStereochemistry010402 general chemistry01 natural sciencesOxalate0104 chemical sciencesCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySpin crossoverPyridineMaterials ChemistryImidazolePhysical and Theoretical ChemistryBimetallic stripPolyhedron
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Experimental and theoretical investigations of the contact ion pairs formed by reactions of the anions [(EPR2)2N]- (R = (i)Pr, (t)Bu; E = S, Se) with…

2010

Reactions of the sodium salts [(EPR(2))(2)N]Na(TMEDA) (R = (i)Pr, (t)Bu; E = S, Se) with the iodide salts [(TePR(2))(2)N]I (R = (i)Pr, (t)Bu) in toluene produce the mixed-chalcogen systems [(EPR(2))(2)N][(TePR(2))(2)N] (6b, E = Se, R = (t)Bu; 6c, E = S, R = (t)Bu; 7b, E = Se, R = (i)Pr; 7c, E = S, R = (i)Pr). Compounds 6b, 6c, 7b, and 7c have been characterized in solution by variable-temperature multinuclear ((31)P, (77)Se, and (125)Te) NMR spectroscopy and in the solid state by single-crystal X-ray crystallography. The structures are comprised of contact ion pairs linked by bonds between Te and S or Se atoms. For the tert-butyl derivatives 6b and 6c, the anionic half of the molecule is co…

chemistry.chemical_classificationDenticityStereochemistryIodideBond orderCoordination complexInorganic ChemistryBond lengthElectron transferCrystallographychemistryIntramolecular forceMoleculePhysical and Theoretical ChemistryInorganic chemistry
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1‑Phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl: The First "Blatter Radical" for Coordination Chemistry

2014

A neutral air- and moisture-stable N,N′-chelating radical ligand, 1-phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl (1) was synthesized and characterized by electron paramagnetic resonance spectroscopy, X-ray crystallography, and magnetic measurements. Subsequent reaction of 1 with Cu(hfac)2·2H2O (hfac = hexafluoroacetylacetonate) under ambient conditions afforded the coordination complex Cu(1)(hfac)2 in which the radical binds to the metal in a bidentate fashion. Magnetic susceptibility data collected from 1.8 to 300 K indicate a strong ferromagnetic metal-radical interaction in the complex and weak antiferromagnetic radical···radical interactions between the Cu(1)(hfac)2 units. Detailed com…

chemistry.chemical_classificationDenticityStereochemistryLigandpysyvät radikaalitRadicalmetal complexes[CHIM.INOR]Chemical Sciences/Inorganic chemistryMedicinal chemistryMagnetic susceptibilityCoordination complexInorganic ChemistryMetalParamagnetismCoordination Chemistrystable radicalschemistryBlatter radikaalivisual_artvisual_art.visual_art_mediumAntiferromagnetismBlatter radicalPhysical and Theoretical Chemistryta116metallikompleksit
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Coordination chemistry of sulfamethizole: crystal structures of [Cu(sulfamethizolate)2(py)2(OH2)]·H2O, [M(sulfamethizolate)2(py)2(OH2)2] [M=Co and Ni…

2000

Abstract The synthesis and characterisation of copper, cobalt, nickel and zinc compounds with sulfamethizole (4-amino-N-(5-methyl-1,3,4-thiadiazole-2-yl)sulfanilamide) (Hsmtz) are described. The first crystal structures of ternary sulfamethizole complexes are reported. The crystal structures of Cu(smtz)2(py)2(OH2)·H2O (1), M(smtz)2(py)2(OH2)2 [M=Co (2), Ni (3)] and {Cu(smtz)2(dmf)2}∞ (5) were determined by X-ray diffraction. The Cu(II) ion exhibits a square pyramidal geometry in complex 1, while in the other compounds the metal ion presents a distorted octahedral environment. In compounds 1, 2 and 3 the deprotonated sulfamethizole acts as monodentate ligand coordinating through the thiadiaz…

chemistry.chemical_classificationDenticitychemistry.chemical_elementSulfamethizoleCrystal structureSquare pyramidal molecular geometryCoordination complexInorganic ChemistryMetalCrystallographyNickelchemistryvisual_artMaterials Chemistrymedicinevisual_art.visual_art_mediumPhysical and Theoretical ChemistryCobaltmedicine.drugPolyhedron
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In vitro evaluation of leishmanicidal properties of a new family of monodimensional coordination polymers based on diclofenac ligand

2020

Some series of isostructural chains with general formula [M(diclof)(HO)]·(EtOH) have been obtained from reaction between diclofenac ligand (diclof) and first row transition salts (M = Mn (1),Ni (2) and Co (3)). These monodimensional coordination polymers have been characterized and their crystal structures have been solved by X-ray diffraction methods, elucidating isostructural compounds that are chains with water molecules acting as bridge between different metallic centers, while diclofenac ligands are coordinated to the octahedral coordination environment of the same. Magnetic studies of these complexes have revealed the existence of moderate ferromagnetic interactions among manganese, n…

chemistry.chemical_classificationDiclofenac010405 organic chemistryLigandMagnetismChainschemistry.chemical_elementTransition metalsCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesCoordination complexInorganic ChemistryCrystallographyNickelTransition metalchemistryOctahedronMaterials ChemistryMoleculePhysical and Theoretical ChemistryIsostructuralLeishmaniasisPolyhedron
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Stable 17-electron Mo(III) complexes containing alkyl ligands

1999

Abstract The alkylation of the half-sandwich complex CpMoCl 2 ( η 4 -diene) (diene=C 4 H 6 , 2,3-Me 2 C 4 H 4 ) affords the first thermally stable 17-electron compounds containing Mo(III)–alkyl bonds.

chemistry.chemical_classificationDiene010405 organic chemistryChemistryMo(III)–alkyl bondsHalf-sandwich complexesElectronAlkylation010402 general chemistry01 natural sciences0104 chemical sciences3. Good health17-electron compoundsInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryOrganic chemistryAlkylation reactions[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryAlkyl
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Peptide metal-organic frameworks under pressure: flexible linkers for cooperative compression

2018

We investigate the structural response of a dense peptide metal-organic framework using in situ powder and single-crystal X-ray diffraction under high-pressures. Crystals of Zn(GlyTyr)2 show a reversible compression by 13% in volume at 4 GPa that is facilitated by the ability of the peptidic linker to act as a flexible string for a cooperative response of the structure to strain. This structural transformation is controlled by changes to the conformation of the peptide, which enables a bond rearrangement in the coordination sphere of the metal and changes to the strength and directionality of the supramolecular interactions specific to the side chain groups in the dipeptide sequence. Compar…

chemistry.chemical_classificationDipeptideCoordination sphereSupramolecular chemistryQuímica organometàl·licaPeptideSequence (biology)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundchemistrySide chainMetal-organic frameworkPèptids0210 nano-technologyLinker
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