Search results for "COPP"

showing 10 items of 3147 documents

Copper(II) and nickel(II) complexes of pyridylamido hexadentate ligands: chemical speciation and spectroscopic studies

2003

Abstract Two novel potentially hexadentate ligands, 1,10-(2-bis picolinamide)-4,7-diazadecane (pycdpnen) and 1,8-bis(2-picolinamide)-3,6-dioxaoctane (pycdado) have been synthesised as their hydrochloride salt; its protonation constants and the stability constants of the copper(II) and nickel(II) chelates have been determined by potentiometry. Amide groups deprotonation permits the formation of [MLH −1 ] + species in all cases, while only pycdado gives [MLH −2 ] species. The solid complexes of copper and nickel with the neutral and the deprotonated ligands have been synthesised and characterised by IR, UV–Vis and ESR spectroscopy. The amidic groups are coordinated through the oxygen atoms in…

chemistry.chemical_classification010405 organic chemistryHydrochlorideInorganic chemistrychemistry.chemical_elementSalt (chemistry)Protonation[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic ChemistryNickelchemistry.chemical_compoundDeprotonationchemistryAmidePolymer chemistryMaterials ChemistryChelation[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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Studies on coordination compounds—VIII. Syntheses, structural, magnetic, spectral and thermal properties of some cobalt(II), nickel(II) and copper(II…

1995

Abstract The complexes bis[triaqua(2-aminopyrimidine)-μ-sulphato-O,O′-cobalt(II)] dihydrate (1), catena-[diaqua(2(2-aminopyrimidine))-μ-sulphato-O,O′nickel(II)]2-amino-pyrimidine (2), [pentaaqua(2-aminopyrimidine)nickel(II)]sulphate 2-aminopyrimidine (3) and catena-[aqua(2(2-aminopyrimidine))-μ-sulphato-O,O′-copper(II)] dihydrate (4) were prepared, structure determined by X-ray methods and physical properties studied by magnetic, IR, NMR, EPR and reflectance methods. The thermal behaviour was studied by TG and mass spectrometric methods. The results are discussed on a structural basis.

chemistry.chemical_classification010405 organic chemistryInorganic chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesMass spectrometricReflectivityCopper0104 chemical scienceslaw.inventionCoordination complexInorganic ChemistryNickelchemistrylawMaterials ChemistryPhysical and Theoretical ChemistryElectron paramagnetic resonanceCobaltNuclear chemistryPolyhedron
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Crystal Engineering Applied to Modulate the Structure and Magnetic Properties of Oxamate Complexes Containing the [Cu(bpca)]+ Cation

2016

This work deals with the crystal engineering features of four related copper(II)-based compounds with formulas {[{Cu(bpca)}2(H2ppba)]·1.33DMF·0.66DMSO}n (2), [{Cu(bpca)(H2O)}2(H2ppba)] (3), [{Cu(bpca)}2(H2ppba)]·DMSO (4), and [{Cu(bpca)}2(H2ppba)]·6H2O (5) [H4ppba = N,N′-1,4-phenylenebis(oxamic acid) and Hbpca = bis(2-pyridylcarbonyl)amide] and how their distinct molecular and crystal structures translate into their different magnetic properties. 2 and 3 were obtained through the hydrolytic reaction of the double-stranded oxamato-based dipalladium(II) paracyclophane precursor of formula [{K4(H2O)2}{Pd2(ppba)2}] (1) with the mononuclear copper(II) complex [Cu(bpca)(H2O)2]+, either in a water…

chemistry.chemical_classification010405 organic chemistryInorganic chemistrychemistry.chemical_elementSalt (chemistry)General ChemistryCrystal structure010402 general chemistryCondensed Matter PhysicsCrystal engineering01 natural sciencesCopper0104 chemical sciencesSolventchemistry.chemical_compoundCrystallographyHydrolysischemistryAmideMoleculeGeneral Materials ScienceCrystal Growth & Design
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Alternating Ferro/Antiferromagnetic Copper(II) Chain Containing an Unprecedented Triple Formato/Hydroxido/Sulfato Bridge.

2016

The first example of a triple formato/hydroxido/sulfato (FHS) bridge for any metal is reported in compound [Cu2(bpym)(OH)(HCO2)(SO4)(H2O)2]·3H2O (1). Its structure shows the presence of alternating triple FHS bridges and 2,2'-bipyrimidine (bpym) ones. Although in the initial synthesis the sulfate anions were introduced accidentally, here we report the rational synthesis and the magnetic properties of this compound. The magnetic properties show that 1 is an alternating ferro/antiferromagnetic (F/AF) chain compound with predominant antiferromagnetic interactions and were fit to an alternating F/AF S = (1)/2 chain with g = 2.103, JAF = -139 cm(-1), and JF = 116 cm(-1) (α = JF/|JAF| = 0.83). Th…

chemistry.chemical_classification010405 organic chemistryStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic ChemistryMetalCrystallographyChain (algebraic topology)chemistryvisual_artvisual_art.visual_art_mediumAntiferromagnetismPhysical and Theoretical ChemistryBridged compoundsInorganic chemistry
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The ultrasounds-ionic liquids synergy on the copper catalyzed azide-alkyne cycloaddition between phenyl acetylene and 4-azidoquinoline

2015

Abstract The effect of ultrasound irradiation on the copper catalyzed azide–alkyne cycloaddition between phenylacetylene and 4-azidoquinoline has been studied in solution of different ionic liquids. In particular, we used ionic liquids featuring both aliphatic and aromatic mono- and dications, as well as anions differing in size, symmetry and coordination ability. We also examined the influence of the ionic liquids structural features on the reaction outcomes, finding that under magnetic stirring reactivity is favorably affected by the solvent structural organization, while under sonochemical conditions an opposite trend was observed. In all cases examined, sonochemical activation leads to …

chemistry.chemical_classificationAcoustics and UltrasonicsChemistryOrganic ChemistryAlkyneSettore CHIM/06 - Chimica Organicaequipment and suppliesPhotochemistryCycloadditionInorganic ChemistrySolventchemistry.chemical_compoundPhenylacetyleneIonic liquidCopper catalyzedChemical Engineering (miscellaneous)Environmental ChemistryRadiology Nuclear Medicine and imagingReactivity (chemistry)AzideIonic liquids Ultrasound irradiation Azide-alkyne cycloaddition
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ChemInform Abstract: Review: Solution Equilibria of Ternary Complexes Formed from Copper(II), Aliphatic Amines, and Bioligands

2014

This review provides a summary of the coordination chemistry of ligands in the ternary system: copper(II)–aliphatic amine–bioligand, where amine = ethylenediamine – En, diethylenetriamine – Dien, or N, N, N′, N″, N″-pentamethyldiethylenetriamine – Me5dien, and bioligand = selected amino acid, aminohydroxamic acid, or aminophosphonic acid, in aqueous solution. We would like to show the specific interactions of copper(II) in ternary systems in the context of complex equilibria chemistry.

chemistry.chemical_classificationAqueous solutionTernary numeral systemchemistry.chemical_elementContext (language use)General MedicineCopperCoordination complexAmino acidchemistry.chemical_compoundchemistryDiethylenetriaminePolymer chemistryTernary operationChemInform
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Low-Temperature Optical Spectroscopy of Native and Azide-Reacted Bovine Cu,Zn Superoxide Dismutase. A Structural Dynamics Study

1994

The optical absorption spectra of native and N(3-)-reacted Cu,Zn superoxide dismutase (SOD) has been studied in the temperature range 300-10 K. The broad d-d bands observed in the room temperature spectrum, centered at 14,700 cm-1 (native enzyme) and at 15,550 cm-1 (N(3-)-reacted enzyme), are clearly split at low temperature into two bands each, centered at 12,835 and 14,844 cm-1 and at 14,418 and 16,300 cm-1, respectively. The thermal behavior of the 23,720 cm-1 band present in the spectrum of the native enzyme indicates that this band belongs to the His61-->Cu(II) ligand to metal charge transfer transition. Analysis of the zeroth, first, and second moments of the various bands as a functi…

chemistry.chemical_classificationAzidesBinding SitesHot TemperatureSuperoxide DismutaseLigandCircular DichroismTemperatureAtmospheric temperature rangeBiochemistryIonCatalysisMetalchemistry.chemical_compoundCrystallographyEnzymechemistrySpectrophotometryvisual_artvisual_art.visual_art_mediumAnimalsCattleAzideSpectroscopyCopperBiochemistry
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Studies on metal-drug complexes. Crystal structure and characterization of μ-sulfato bromazepam copper(II) complex

1987

Abstract The compound Cu(Bromazepam) SO 4 having been synthesized, its crystal structure shows distorted octahedral environment for the Copper(II) ion. Because of the long Cu-O(4) length (2.90 A), we can consider that there is a semicoordinative interaction with the sulfate group acting as tridentate bridging ligand. The structure is a polymeric chain where dimeric units are linked by the oxygen (C-O(5)) atom of the Bromazepam carbonyl group. The drug consequently acts as a tridentate ligand in this compound. The magnetic results show a very weak antiferromagnetic interaction.

chemistry.chemical_classificationBromazepamChemistryStereochemistrychemistry.chemical_elementBridging ligandCrystal structureBiochemistryCopperInorganic ChemistryMetalCrystallographyOctahedronvisual_artmedicinevisual_art.visual_art_mediumMoleculeInorganic compoundmedicine.drugJournal of Inorganic Biochemistry
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Effect of ethylenediamine on the anodic stripping voltammetric determination of heavy metals in the presence of humic acid

1994

Ligand competition coupled with differential pulse anodic stripping voltammetry has been investigated for the determination of copper, lead and cadmium. Ethylenediamine displaces humic acid in its metal complexes forming kinetically labile compounds. It also eliminates interferences associated with the oxidation of copper. This enhances the sensitivity of the determination of the metals over a wide range of humic acid concentration (up to 30 mg/l). The procedure has been applied to the determination of heavy metals in a real water sample.

chemistry.chemical_classificationCadmiumStripping (chemistry)LigandInorganic chemistrychemistry.chemical_elementEthylenediaminecomplex mixturesBiochemistryCopperAnalytical ChemistryMetalAnodic stripping voltammetrychemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumHumic acidFresenius' Journal of Analytical Chemistry
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Alkyl- and aryl-substituted corroles. 5. Synthesis, physicochemical properties, and X-ray structural characterization of copper biscorroles and porph…

2004

The synthesis and characterization of cofacial copper biscorroles and porphyrin-corroles linked by a biphenylenyl or anthracenyl spacer are described. The investigated compounds are represented as (BCA)Cu(2) and (BCB)Cu(2) in the case of the biscorrole (BC) derivatives and (PCA)Cu(2) and (PCB)Cu(2) in the case of porphyrin (P)-corrole (C) dyads, where A and B represent the anthracenyl and biphenylenyl bridges, respectively. A related monomeric corrole (Me(4)Ph(5)Cor)Cu and monomeric porphyrin (Me(2)Et(6)PhP)Cu that comprise the two halves of the porphyrin-corrole dyads were also studied. Electron spin resonance (ESR), (1)H NMR, and magnetic measurements data demonstrate that the copper corr…

chemistry.chemical_classificationChemistryArylchemistry.chemical_elementPhotochemistryCopperPorphyrinlaw.inventionInorganic Chemistrychemistry.chemical_compoundOxidation statelawPolymer chemistryProton NMRPhysical and Theoretical ChemistryCorroleElectron paramagnetic resonanceAlkylInorganic chemistry
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