Search results for "COPP"

showing 10 items of 3147 documents

Copper nanowire array as highly selective electrochemical sensor of nitrate ions in water

2020

Contamination of water with nitrate ions is a significant problem that affects many areas of the world. The danger from nitrates is not so much their toxicity, rather low, as their transformation into nitrites and in particular into nitrosamines, substances considered to be a possible carcinogenic risk. For this reason, European legislation has set the maximum permissible concentration of nitrates in drinking water at 44 mg/l. Thus, it is clear that a continuous monitoring of nitrate ions is of high technological interest but it must be rapid, easy to perform and directly performed in situ. Electrochemical detection is certainly among the best techniques to obtain the above requirements. In…

Nitrate ionMaterials scienceInorganic chemistrychemistry.chemical_element02 engineering and technology01 natural sciencesChlorideAnalytical ChemistryIonCopper nanowireschemistry.chemical_compoundNitrateSettore ING-IND/17 - Impianti Industriali MeccaniciChlorinemedicineSolubilityDetection limitPrecipitation (chemistry)010401 analytical chemistry021001 nanoscience & nanotechnologyCopperNanostructures0104 chemical sciencesElectrochemical gas sensorGalvanic depositionSettore ING-IND/23 - Chimica Fisica ApplicataElectrochemical sensorchemistry0210 nano-technologyWater contaminationmedicine.drugTalanta
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Synthesis, X-ray crystal structure and magnetic study of a μ 1,5-dca bridged ferromagnetic dimeric copper(II) complex

2008

Reaction of Cu(NO3)2 · 3H2O, 1-(N-salicyalideneimine)-2-(N,N-dimethyl)-aminoethane (HL1), LiClO4, and sodium dicyanamide (Nadca) in aqueous medium affords a dimeric complex [Cu2(L1)2 (μ1, 5-dca)](ClO4) (1). Single crystal X-ray analysis reveals that 1 is dinuclear with copper(II) ions bridged by a single dicyanamide group in end-to-end fashion. The coordination environment around copper(II) is square planar. Two nitrogens and oxygen of the tridentate Schiff-base ligand (HL1) occupy three coordination sites of the square plane while the remaining site is occupied by the nitrogen of a terminal nitrile of the bridging dca. The nitrogen of the other terminal nitrile group of the μ1,5-dca ligand…

NitrileStereochemistryDimerchemistry.chemical_elementCrystal structureMagnetic susceptibilityCopperchemistry.chemical_compoundCrystallographychemistryFerromagnetismMaterials ChemistryPhysical and Theoretical ChemistryDicyanamideSingle crystalJournal of Coordination Chemistry
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TCNQ radical salts containing magnetic complexes: Different interaction modes of TCNQ with Copper tetraazamacrocycles

1997

Abstract This work is devoted to the study of compounds [M(N 4 )](TCNQ) n , where N 4 = saturated or unsaturated tetraazamacrocycles, TCNQ= 7,7,8,8-tetracyanoquinodimethane, n= 2, 3. The metal is coordinated to two TCNQ groups only when there is coordinative unsaturation on it. When n= 2 all the TCNQ units are radical anions and no charge delocalization is observed. In the compounds with n= 3 only 2 3 of the TCNQ are negatively charged and a greater charge delocalization is possible. This delocalization only appears when none of the TCNQ's are coordinated to the metal and it is reflected in the higher conductivity values obtained in the solid state.

NitrilebiologyChemistryMechanical EngineeringInorganic chemistryMetals and Alloyschemistry.chemical_elementConductivityCondensed Matter PhysicsCopperMagnetic susceptibilityElectronic Optical and Magnetic MaterialsMetalchemistry.chemical_compoundCrystallographyDelocalized electronMechanics of MaterialsElectrical resistivity and conductivityvisual_artMaterials Chemistryvisual_art.visual_art_mediumbiology.proteinOrganic anionSynthetic Metals
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A catalytic highly enantioselective direct synthesis of 2-bromo-2-nitroalkan-1-ols through a Henry reaction.

2008

Highly enantiomerically enriched 2-bromo-2-nitroalkan-1-ols are prepared by direct condensation of aliphatic and aromatic aldehydes with bromonitromethane in the presence of a catalytic amount of copper(II) acetate and a C1-symmetric camphorderived amino pyridine ligand. Blay Llinares, Gonzalo, Gonzalo.Blay@uv.es ; Hernandez Olmos, Victor, Victor.Hernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es

Nitroaldol reactionEnrichedCondensationPyridinesBromonitromethaneUNESCO::QUÍMICACatalytic ; Synthesis ; Henry reaction ; Enriched ; CondensationMolecular Conformationchemistry.chemical_elementAcetatesLigands:QUÍMICA [UNESCO]CatalysisCatalysisSynthesisMaterials ChemistryOrganic chemistryCatalyticAldehydesEthaneChemistryUNESCO::QUÍMICA::Química inorgánicaCondensationMetals and AlloysEnantioselective synthesisStereoisomerismGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Nitro CompoundsCopperPyridine ligandSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAlcoholsCeramics and CompositesHenry reactionCopperChemical communications (Cambridge, England)
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Metal-Organic Frameworks as Versatile Heterogeneous Solid Catalysts for Henry Reactions

2021

Metal–organic frameworks (MOFs) have become one of the versatile solid materials used for a wide range of applications, such as gas storage, gas separation, proton conductivity, sensors and catalysis. Among these fields, one of the more well-studied areas is the use of MOFs as heterogeneous catalysts for a broad range of organic reactions. In the present review, the employment of MOFs as solid catalysts for the Henry reaction is discussed, and the available literature data from the last decade are grouped. The review is organized with a brief introduction of the importance of Henry reactions and structural properties of MOFs that are suitable for catalysis. The second part of the review dis…

Nitroaldol reactionMaterials sciencePharmaceutical ScienceReviewHeterogeneous catalysisCatalysisAnalytical ChemistryCatalysislcsh:QD241-441metal–organic frameworkslcsh:Organic chemistryCatalytic DomainDrug DiscoveryUreaGas separationAminesPhysical and Theoretical ChemistryMetal-Organic FrameworksHeterogeneous catalysisPrimary (chemistry)Organic ChemistryAmidesOrganic reactionChemical engineeringChemistry (miscellaneous)Molecular MedicineMetal-organic frameworkAmine gas treatingHenry reactionCopperMolecules
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Modular iminopyridine ligands. Application to the enantioselective copper(II)-catalyzed Henry reaction

2006

Abstract Chiral iminopyridines prepared in a modular fashion from monoterpenic (camphor-derived) ketones and pyridinylalkylamines catalyze the enantioselective Henry (nitro aldol) reaction between nitromethane and o -anisol in the presence of copper(II) acetate, with high yields and good ee (up to 86%) under straightforward experimental conditions without the need for air or moisture exclusion.

Nitroaldol reactionNitromethaneOrganic ChemistryEnantioselective synthesischemistry.chemical_elementCopperCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryAldol reactionNitroOrganic chemistryPhysical and Theoretical ChemistryTetrahedron: Asymmetry
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Enantioselective Henry reaction catalyzed with copper(II)–iminopyridine complexes

2007

Abstract Copper complexes of chiral iminopyridines prepared from camphane-derived ketones and picolylamine catalyzed the enantioselective Henry (nitroaldol) reaction between nitromethane and a number of aromatic and aliphatic aldehydes with high yields and good enantioselectivities. Iminopyridines derived from (1 R )-(+)-camphor and (1 S )-(+)-ketopinic acid gave the best results to afford the opposite enantiomers in each case, despite the fact they have the same stereochemical pattern at the camphane skeleton. The reactions were carried out without air or moisture exclusion.

Nitroaldol reactionNitromethaneOrganic ChemistryEnantioselective synthesischemistry.chemical_elementGeneral MedicineMedicinal chemistryCopperCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryOrganic chemistryPhysical and Theoretical ChemistryEnantiomerTetrahedron: Asymmetry
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New highly asymmetric Henry reaction catalyzed by Cu(II) and a C(1)-symmetric aminopyridine ligand, and its application to the synthesis of miconazol…

2008

A new catalytic asymmetric Henry reaction has been developed that uses a C(1)-symmetric chiral aminopyridine ligand derived from camphor and picolylamine. A variety of aromatic, heteroaromatic, aliphatic, and unsaturated aldehydes react with nitromethane and other nitroalkanes in the presence of DIPEA (1.0 equiv), Cu(OAc)(2)*H(2)O (5 mol %), and an aminopyridine ligand (5 mol %) to give the expected products in high yields (up to 99 %), moderate-to-good diastereoselectivites (up to 82:18), and excellent enantioselectivities (up to 98 %). The reaction is air-tolerant and has been used in the synthesis of the antifungal agent miconazole.

Nitroaldol reactionNucleophilic additionNitromethaneMiconazoleMolecular StructureChemistryLigandOrganic ChemistryEnantioselective synthesisStereoisomerismStereoisomerismGeneral ChemistryLigandsMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundAldol reactionOrganic chemistry4-AminopyridineCopperChemistry (Weinheim an der Bergstrasse, Germany)
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DNP in MRI: an in-bore approach at 1.5 T.

2011

Abstract We have used liquid state (“Overhauser”) Dynamic Nuclear Polarization (DNP) to significantly enhance the signal to noise ratio (SNR) of Magnetic Resonance Imaging (MRI). For the first time this was achieved by hyperpolarizing directly in the MRI-scanner field of 1.5 T in continuous flow mode and immediately delivering the hyperpolarized substance to the imaging site to ensure maximum contrast between hyperpolarized sample and sample at thermal polarization. We achieve a maximum absolute signal enhancement factor of 98; while the hyperpolarized sample is transported at a flow rate of up to 30 ml/h yielding an average flow speed up to 470 mm/s over a distance of approximately 80 mm. …

Nuclear and High Energy PhysicsContrast enhancementMagnetic Resonance Spectroscopymedicine.diagnostic_testContinuous flowChemistryPhantoms ImagingBiophysicsMagnetic resonance imagingSignal-To-Noise RatioCondensed Matter PhysicsPolarization (waves)BiochemistryMagnetic Resonance ImagingVolumetric flow rateSignal enhancementCyclic N-OxidesLiquid stateNuclear magnetic resonanceFlow velocitymedicineImage Processing Computer-AssistedSpin LabelsMicrowavesCopperJournal of magnetic resonance (San Diego, Calif. : 1997)
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Isomer separation of Cu and Cu with a resonance ionization laser ion source

2000

Abstract Radioactive copper isotopes were ionized with the resonance ionization laser ion source (RILIS) at the on-line isotope separator ISOLDE (CERN). Using the different hyperfine structure in the 3d10 4s  2 S1/2 – 3d10 4p  2 P01/2 transition the low- and high-spin isomers of 70 Cu were selectively enhanced by tuning the laser wavelength. The light was provided by a narrow-bandwidth dye laser pumped by copper vapor lasers (CVL) and frequency doubled in a BBO crystal. The ground state to isomeric state intensity ratio could be varied by a factor of 30, allowing to assign gamma transitions unambiguously to the decay of the individual isomers. It is shown that the method can also be used to…

Nuclear and High Energy PhysicsDye laserIsotopes of copperChemistryAnalytical chemistryPhysics::OpticsLaserIon sourcelaw.inventionlawIonizationPhysics::Atomic PhysicsAtomic physicsGround stateAtomic vapor laser isotope separationInstrumentationHyperfine structure
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