Search results for "complex"

showing 10 items of 5889 documents

Bis{3,5-di-tert-butyl-N-[(4-dimethylamino)phenyl]salicylaldiminato}cobalt(II)

2017

In the title complex [systematic name: bis(2,4-di-tert-butyl-6-{N-[4-(dimethylamino)phenyl]carboximidoyl}phenolato)cobalt(II)], [Co(C23H31N2O)2], the cobalt(II) atom is coordinated by pairs of O and N atoms in a distorted tetrahedral coordination geometry. The dihedral angles formed by the aromatic rings of the same ligand are 51.99 (11) and 36.58 (9)°. The molecular conformation features weak intramolecular C—H...O hydrogen bonds. In the crystal, inversion-related pairs of complex molecules are linked into dimers by weak C—H...π interactions. The methyl C atoms oftert-butyl groups have rotational disorder, with site occupancies of 0.647 (7) and 0.617 (6) for the major components and 0.353 …

crystal structureHydrogen bondLigandchemistry.chemical_elementAromaticityCrystal structureDihedral angle010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencescobalt(II) complex0104 chemical sciencesCrystalCrystallographychemistrylcsh:QD901-999lcsh:Crystallographydistorted tetrahedral geometryCobaltCoordination geometryIUCrData
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Bis(4,6-di-tert-butyl-2-{N-[4-(diethylamino)phenyl]carboximidoyl}phenolato)cobalt(II)

2017

In the title complex, [Co(C25H35N2O)2], the cobalt(II) atom has a distorted tetrahedral geometry provided by pairs of O and N atoms. The dihedral angles between the benzene rings of the same ligand are 52.39 (9) and 34.96 (9)°. The molecular structure is stabilized by weak intramolecular C—H...O hydrogen bonds. The crystal packing is stabilized mainly by van der Waals forces. The structure contains a solvent-accessible void of 276 Å3which was treated using the SQUEEZE routine fromPLATON[Spek (2015).Acta Cryst.C71, 9–18]. The methyl C atoms of thetert-butyl groups are rotationally disordered, with site occupancies of 0.802 (3) and 0.548 (9) for the major components and 0.198 (3) and 0.452 (9…

crystal structureHydrogen bondchemistry.chemical_elementCrystal structureDihedral angle010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencescobalt(II) complex0104 chemical scienceschemistry.chemical_compoundsymbols.namesakeCrystallographychemistryAtomlcsh:QD901-999symbolslcsh:Crystallographyvan der Waals forceBenzenedistorted tetrahedral geometryCobaltIUCrData
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A Gadolinium(III) Complex Based on the Thymine Nucleobase with Properties Suitable for Magnetic Resonance Imaging

2021

The paramagnetic gadolinium(III) ion is used as contrast agent in magnetic resonance (MR) imaging to improve the lesion detection and characterization. It generates a signal by changing the relaxivity of protons from associated water molecules and creates a clearer physical distinction between the molecule and the surrounding tissues. New gadolinium-based contrast agents displaying larger relaxivity values and specifically targeted might provide higher resolution and better functional images. We have synthesized the gadolinium(III) complex of formula [Gd(thy)2(H2O)6](ClO4)3·2H2O (1) [thy = 5-methyl-1H-pyrimidine-2,4-dione or thymine], which is the first reported compound based on gadolinium…

crystal structureMaterials scienceMagnetometerQH301-705.5GadoliniumContrast Mediachemistry.chemical_elementmetal complexesCrystallography X-Ray010402 general chemistry01 natural sciencesArticleCatalysisIonNucleobaselaw.inventionInorganic Chemistrymagnetic resonanceMagneticsParamagnetismchemistry.chemical_compoundNuclear magnetic resonanceHeterocyclic CompoundslawthyminemedicineMoleculePhysical and Theoretical ChemistryBiology (General)Molecular BiologyQD1-999SpectroscopyMolecular Structuremedicine.diagnostic_test010405 organic chemistryOrganic ChemistryWaterMagnetic resonance imagingGeneral Medicinecontrast agentMagnetic Resonance Imaging0104 chemical sciencesComputer Science ApplicationsThymineChemistrychemistryrelaxivityProtonsgadolinium
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Crystal structure of chlorido(2-{1-[2-(4-chlorophenyl)hydrazin-1-ylidene-κN]ethyl}pyridine-κN)(η5-pentamethylcyclopentadienyl)rhodium(III) chloride

2015

The title compound, [Rh(η5-C5Me5)Cl(C13H12ClN3)]Cl, is chiral at the metal and crystallizes as a racemate. Upon coordination, the hydrazinyl­idene­pyridine ligand is non-planar, an angle of 54.42 (7)° being observed between the pyridine ring and the aromatic ring of the [2-(4-chloro­phen­yl)hydrazin-1-yl­idene]ethyl group.

crystal structureNanotechnologyCrystal structureRing (chemistry)Medicinal chemistryResearch CommunicationsMetalpenta­methyl­cyclo­penta­dien­yllcsh:Chemistrychemistry.chemical_compoundPyridinepiano-stool geometryGeneral Materials SciencepentamethylcyclopentadienylEthyl grouprhodium(III) complexN—H⋯Cl hydrogen bondHydrogen bondLigandGeneral ChemistryRhodium(III) chlorideN—H...Cl hydrogen bondCondensed Matter Physicschemistrylcsh:QD1-999visual_artvisual_art.visual_art_mediumActa Crystallographica Section E: Crystallographic Communications
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Ferro- and Antiferromagnetic Interactions in Oxalato-Centered Inverse Hexanuclear and Chain Copper(II) Complexes with Pyrazole Derivatives.

2021

Two novel copper(II) complexes of formulas {[Cu(4-Hmpz)4][Cu(4-Hmpz)2(µ3-ox-κ2O1,O2:κO2′:κO1′)(ClO4)2]}n (1) and {[Cu(3,4,5-Htmpz)4]2[Cu(3,4,5-Htmpz)2(µ3-ox-κ2O1,O2:κO2′:κO1′)(H2O)(ClO4)]2[Cu2(3,4,5-Htmpz)4(µ-ox-κ2O1,O2:κ2O2′,O1′)]}(ClO4)4·6H2O (2) have been obtained by using 4-methyl-1H-pyrazole (4-Hmpz) and 3,4,5-trimethyl-1H-pyrazole (3,4,5-Htmpz) as terminal ligands and oxalate (ox) as the polyatomic inverse coordination center. The crystal structure of 1 consists of perchlorate counteranions and cationic copper(II) chains with alternating bis(pyrazole)(µ3-κ2O1,O2:κO2′:κO1′-oxalato)copper(II) and tetrakis(pyrazole)copper(II) fragments. The crystal structure of 2 is made up of perchlorat…

crystal structurePharmaceutical Sciencechemistry.chemical_elementCrystal structurePyrazoleOxalateArticleAnalytical ChemistryPerchloratechemistry.chemical_compoundQD241-441TheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYDrug DiscoveryAntiferromagnetismPhysical and Theoretical Chemistrypolynuclear complexesOrganic ChemistryPolyatomic ioninverse coordination chemistryoxalatoCopperpyrazoleCrystallographycoordination polymerschemistryChemistry (miscellaneous)Intramolecular forcecopperMolecular Medicinemagnetic propertiesMolecules (Basel, Switzerland)
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Crystal structure of catena-poly[[[(2-ethoxypyrazine-κN)copper(I)]-di-μ2-cyanido] [copper(I)-μ2-cyanido]]

2019

The title compound, {[Cu(EtOpz)(CN)2][CuCN]}n, where EtOpz is 2-eth­oxy­pyrazine, is a two-dimensional polymeric copper complex with different coordination environments of the two CuI ions. One Cu atom is coordinated to the 2-eth­oxy­pyrazine mol­ecule and two bridging cyanide ligands, equally disordered over two sites. The second Cu atom is coordinated by two disordered over two sites bridging cyanide groups. Two copper–cyanide chains are connected through Cu⋯Cu contact.

crystal structurePyrazineCyanidechemistry.chemical_elementeth­oxy­pyrazineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesResearch CommunicationsCoordination complexmetal–organic frameworkchemistry.chemical_compoundAtomGeneral Materials ScienceCoordination geometrychemistry.chemical_classificationCrystallographyethoxypyrazinecyanidesGeneral ChemistryCondensed Matter PhysicsCoppercopper(I)0104 chemical sciencesCrystallographychemistryQD901-999Metal-organic frameworkActa Crystallographica Section E Crystallographic Communications
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Stabilisation of Exotic Tribromide (Br3−) Anions via Supramolecular Interaction with A Tosylated Macrocyclic Pyridinophane. A Serendipitous Case.

2020

Tetraaza-macrocyclic pyridinophane L-Ts, decorated with a p-toluenesulfonyl (tosyl

crystal structureStackingSupramolecular chemistryPharmaceutical ScienceCrystal structureAnalytical Chemistrylcsh:QD241-441symbols.namesakechemistry.chemical_compoundlcsh:Organic chemistryTosylDrug DiscoveryPyridineHirshfeld surface analysisPhysical and Theoretical ChemistryN-heterocyclesanion- interactionsTribromideHydrogen bondOrganic Chemistryanion complexesCrystallographychemistryChemistry (miscellaneous)symbolsMolecular Medicinevan der Waals forceMolecules
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Crystal structure of bis­(2-methyl-1H-imidazol-3-ium) di­hydroxidobis(oxalato-κ2 O 1,O 2)stannate(IV) monohydrate

2016

The SnIV atom in the anion of the title compound is six-coordinated by two OH groups and four O atoms from two chelating oxalate ligands. Several N—H⋯O and O—H⋯O hydrogen bonds involving the stannate dianions, the cations and the water mol­ecules result into a three-dimensional network structure.

crystal structureStannateorganotin(IV) complexInorganic chemistrySalt (chemistry)Crystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences[ CHIM ] Chemical SciencesOxalateResearch Communicationschemistry.chemical_compound[CHIM]Chemical SciencesGeneral Materials ScienceChelationchemistry.chemical_classificationCrystallographyHydrogen bondGeneral ChemistryCondensed Matter PhysicsAcceptor3. Good health0104 chemical sciencesCrystallographychemistryQD901-999hydrogen bondsHydroxideActa Crystallographica Section E: Crystallographic Communications
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Three phenanthroline-metal complexes with topologically similar but geometrically different conformations.

2016

Two out of the three very similar complexes described present twofold symmetry but not the third one, probably by way of a strong intra­molecular C—H⋯O hydrogen bond disrupting the symmetry, a fact which is analysed in detail.

crystal structureStereochemistryPhenanthrolinechemistry.chemical_elementZincCrystal structureQuímica Inorgánica y Nuclear010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesstrong C—H⋯O intra­molecular hydrogen bondsCRYSTAL STRUCTUREResearch Communicationslcsh:ChemistryMetalBase (group theory)//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundGroup (periodic table)strong C—H...O intramolecular hydrogen bondsCd and Zn complexesPEROXODISULFATE ANION//purl.org/becyt/ford/1.4 [https]General Materials ScienceSTRONG C - H⋯O INTRAMOLECULAR HYDROGEN BONDSCadmiumHydrogen bondCiencias QuímicasGeneral ChemistryCondensed Matter Physicsperoxodisulfate anion0104 chemical sciencesCrystallographylcsh:QD1-999chemistryvisual_artvisual_art.visual_art_mediumperoxodi­sulfate anionCD AND ZN COMPLEXESCIENCIAS NATURALES Y EXACTASActa crystallographica. Section E, Crystallographic communications
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Crystal structure of bis[μ-1,4-bis(diphenylphosphanyl)butane-κ2P:P′]bis[(3,4,7,8-tetramethyl-1,10-phenanthroline-κ2N,N′)copper(I)] bis(hexafluoridoph…

2016

The dication of the title compound, [Cu2(C28H28P2)2(C16H16N2)2](PF6)2·2CH2Cl2, has crystallographically imposed inversion symmetry. The copper(I) cation is coordinated in a distorted tetrahedral geometry by two N atoms of a chelating 3,4,7,8-tetramethyl-1,10-phenanthroline ligand and two P atoms of two bridging 1,4-bis(diphenylphosphanyl)butane ligands, forming a 14-membered ring. An intramolecular π–π interaction stabilizes the conformation of the dication. In the crystal, dications are linked by π–π interactions involving adjacent phenanthroline rings, forming chains running parallel to [111]. Weak C—H...F hydrogen interactions are also observed.

crystal structureStereochemistryPhenanthrolinediiminecopper(I) complexesCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistrylcsh:Chemistrychemistry.chemical_compoundDiphosphinesGeneral Materials ScienceDiimineChemistryLigandButaneGeneral ChemistryCondensed Matter PhysicsHEXA0104 chemical sciencesDicationlcsh:QD1-999π–π interactionsdiphosphinesActa Crystallographica Section E: Crystallographic Communications
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