Search results for "COPP"

showing 10 items of 3147 documents

Solid state polymerization causing transition to a ferromagnetic state. Crystal structures and magnetic properties of [Cu2(dpp)(H2O)(dmso)Cl4]·dmso a…

2001

The preparation, crystal structures and variable-temperature magnetic susceptibility data for [Cu2(dpp)(H2O)(dmso)Cl4]·dmso (1a) and [Cu2(dpp)Cl4]n (2) (dpp = 2,3-bis(2-pyridyl)pyrazine, dmso = dimethyl sulfoxide) are reported. 1a consists of dinuclear dpp-bridged molecules with chlorine, water and dmso serving as terminal ligands. The two copper atoms are crystallographically independent, with distorted square pyramidal and trigonal bipyramidal coordination geometries, respectively. In a first approximation 2 may be described as a chain compound with out-of-plane mono-μ-chloro bridges (Cu–Cl–Cu–Cl). Only one of the crystallographically independent copper atoms participates in this chain fo…

PyrazineStereochemistrychemistry.chemical_elementSulfoxideGeneral ChemistryCrystal structureCopperMagnetic susceptibilitySquare pyramidal molecular geometryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographychemistryIsostructuralJournal of the Chemical Society, Dalton Transactions
researchProduct

2-Alkenoyl Pyridine N-Oxides, Highly Efficient Dienophiles for the Enantioselective Cu(II)−Bis(oxazoline) Catalyzed Diels−Alder Reaction

2007

2-Alkenoyl pyridine N-oxides are introduced as a new kind of efficient dienophiles for the Cu(II)−bis(oxazoline) (BOX) catalyzed enantioselective Diels−Alder reaction affording higher reactivity and enantioselectivity (ee's up to 96%) than the corresponding nonoxidized 2-alkenoyl pyridines.

PyridinesCyclopentanesOxazolineAlkenesMedicinal chemistryBiochemistryCatalysisCatalysischemistry.chemical_compoundChalconeIsomerismPyridineOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryOxazolesDiels–Alder reactionchemistry.chemical_classificationAza CompoundsMolecular StructureChemistryOrganic ChemistryEnantioselective synthesisGeneral MedicineBridged compoundsCopperOrganic Letters
researchProduct

Metamagnetism in hydrophobically induced carboxylate (phenylmalonate)-bridged copper(II) layers

2006

Self-assembly of copper(II) ions, phenylmalonate and pyrimidine yields the layered compound [Cu(pym)(Phmal)]n ( 1) where intralayer ferro- and interlayer antiferromagnetic interactions occur with three-dimensional antiferromagnetic ordering at Tc = 2.15 K Lloret Pastor, Francisco, Francisco.Lloret@uv.es ; Julve Olcina, Miguel, Miguel.Julve@uv.es

PyrimidineUNESCO::QUÍMICAInorganic chemistrychemistry.chemical_element:QUÍMICA [UNESCO]CatalysisIonMetamagnetism ; Hydrophobically ; Copper ; Three-dimensional antiferromagneticchemistry.chemical_compoundThree-dimensional antiferromagneticMaterials ChemistryAntiferromagnetismCarboxylateMetamagnetismChemistryUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryHydrophobicallyCopperSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMetamagnetismCrystallographyCeramics and Composites:QUÍMICA::Química analítica [UNESCO]Copper
researchProduct

Bis(4-methylthio)phenylthiomethane as assembling ligand for the construction of Cu(I) and Hg(II) coordination polymers. Crystal structures and topolo…

2016

International audience; The novel 1D coordination polymer (CP) [{Cu(mu(2)-Br)(2)Cu}(mu-L2)(2)] CP2 has been obtained by reaction of the tetrakisthioether p-MeSC6H4SCH2SC6H4SMe-p (L2) with CuBr in a 1: 2 metal-to ligand ratio. In contrast to the previously described CP [{Cu(mu(2)-Br)(2)Cu}(mu-L1)(2)] CP1 obtained by reaction of the tetrakisthioether p-MeOC6H4SCH2SC6H4OMe-p (L1) with CuBr, the two independent extended 1D ribbons contain bent Cu(mu(2)-Br)(2)Cu units of the butterfly-type with short Cu center dot center dot center dot Cu separations of 2.679(1) and 2.613(1) angstrom. In contrast to the common planar rhomboid Cu(mu(2)-Br)(2)Cu cluster, this butterfly-shaped geometry of the core …

QT-AIMLuminescenceCoordination polymerStereochemistryCoordination number[ PHYS.ASTR ] Physics [physics]/Astrophysics [astro-ph]StackingCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencesdinuclear copper(i) complexesInorganic Chemistrychemistry.chemical_compoundelectron-densityThioetheraryl substitutionMaterials Chemistry[CHIM]Chemical Sciencescluster-sizePhysical and Theoretical Chemistrytetrathioether complexesComputingMilieux_MISCELLANEOUSThioether complexesluminescence properties010405 organic chemistrypi-pi stackingAtoms in moleculescu-i interaction[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryMercury0104 chemical sciencesCoordination polymersCrystallographychemistryCovalent bondextended 1dStoichiometryCoppermetal-complexes
researchProduct

Field-induced ferromagnetism due to magneto-striction in 1-D helical chains

2016

Two homochiral copper(II) helices, [Cu(μ1,3-N3)(L1)]n (1) and [Cu(μ1,3-NCO)(L2)]n (2), with end-to-end pseudohalide bridges, were synthesized using two N2O donor achiral Schiff bases via spontaneous chiral resolution. Field-induced ferromagnetic ordering due to magneto-striction in homochiral 1-D helix [Cu(μ1,3-N3)(L1)]n (1) is reported for the first time. At temperatures below 5.5 K, under a magnetic field of 1 T, orthogonality between the magnetic orbitals of copper centres increases significantly due to the contraction of lattice parameters, giving rise to long-range ferromagnetic ordering in the helical chain. The magneto-dielectric results are also indicative of the observed magneto-st…

Quantitative Biology::BiomoleculesCondensed matter physicsChemistryGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCopperChiral resolutionHelical chain0104 chemical sciencesMagnetic fieldfield-induced ferromagnetismCrystallographyFerromagnetismAtomic orbitalLattice (order)Helix0210 nano-technologyta116RSC Advances
researchProduct

Production of π0 and η mesons in Cu+Au collisions at sNN=200GeV

2018

Production of π0 and η mesons has been measured at midrapidity in Cu+Au collisions at sNN=200GeV. Measurements were performed in π0(η)→γγ decay channel in the 1(2)-20GeV/c transverse momentum range. A strong suppression is observed for π0 and η meson production at high transverse momentum in central Cu+Au collisions relative to the p+p results scaled by the number of nucleon-nucleon collisions. In central collisions the suppression is similar to Au+Au with comparable nuclear overlap. The η/π0 ratio measured as a function of transverse momentum is consistent with mT-scaling parametrization down to pT=2GeV/c, its asymptotic value is constant and consistent with Au+Au and p+p and does not show…

Quantum chromodynamicsPhysicsMapleMeson productionMeson010308 nuclear & particles physicsNuclear Theorychemistry.chemical_elementengineering.material16. Peace & justice01 natural sciencesCopperNuclear physicsFragmentation (mass spectrometry)chemistry0103 physical sciencesQuark–gluon plasmaengineeringHigh Energy Physics::ExperimentImpact parameterNuclear Experiment010306 general physicsPhysical Review C
researchProduct

Glycine-functionalized copper(ii) hydroxide nanoparticles with high intrinsic superoxide dismutase activity

2017

Superoxide dismutases (SOD) are a group of enzymes that catalyze the dismutation of superoxide (O2−) radicals into molecular oxygen (O2) and H2O2 as a first line of defense against oxidative stress. Here, we show that glycine-functionalized copper(II) hydroxide nanoparticles (Gly-Cu(OH)2 NPs) are functional SOD mimics, whereas bulk Cu(OH)2 is insoluble in water and catalytically inactive. In contrast, Gly-Cu(OH)2 NPs form water-dispersible mesocrystals with a SOD-like activity that is larger than that of their natural CuZn enzyme counterpart. Based on this finding, we devised an application where Gly-Cu(OH)2 NPs were incorporated into cigarette filters. Cigarette smoke contains high concent…

RadicalInorganic chemistryGlycine02 engineering and technology010402 general chemistrymedicine.disease_cause01 natural sciencesSuperoxide dismutasechemistry.chemical_compoundSmokeHydroxidesmedicineHumansGeneral Materials ScienceReactive nitrogen specieschemistry.chemical_classificationCopper(II) hydroxideReactive oxygen speciesbiologySuperoxide DismutaseSuperoxideHydrogen PeroxideTobacco Products021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryA549 Cellsbiology.proteinNanoparticlesHydroxideReactive Oxygen Species0210 nano-technologyCopperOxidative stressNanoscale
researchProduct

Control of matrix interferences by the multiple linear regression model in the determination of arsenic, antimony and tin in lead pellets by inductiv…

2002

A multiple linear regression technique was used to evaluate the matrix interferences in the determination of hydride-forming elements in lead shotgun pellets by inductively coupled plasma atomic emission spectrometry. The determination of arsenic, antimony, and tin in SRM C2416 (Bullet Lead) by ICP-AES failed to obtain the certified concentrations at the 95% level of confidence using the t-test. However, it proved possible, by using the multiple linear regression technique, to correct the concentrations of all three elements to a statistically acceptable level. This method of correction is based on the multiple regression line obtained from the analysis of 19 synthetic mixtures of matrix el…

RadiochemistryAnalytical chemistrychemistry.chemical_elementequipment and suppliesCopperAnalytical ChemistryBismuthMatrix (chemical analysis)chemistryAntimonyLinear regressionInductively coupled plasmaTinSpectroscopyArsenicJ. Anal. At. Spectrom.
researchProduct

Synthesis of Optically Pure Arylamine Derivatives by Using the Bucherer Reaction

2017

The Bucherer reaction is a common pathway for the conversion of 1- and 2-naphthols into the corresponding 1- or 2-naphthylamines, respectively. Mostly, only singular examples for its preparative use are reported since this particular transformation seems to be very sensitive to the reaction conditions. By choosing different phenolic substrates and chiral amines, we were able to prepare a broad scope of optically pure arylamines using this type of reaction. In contrast to alternative methods forming C−N aryl bonds such as Buchwald-Hartwig or Chan-Lam cross-coupling reactions, no palladium or copper catalysts are required. The use of water as solvent and the easily available starting material…

Reaction conditionsAlternative methodsBucherer reaction010405 organic chemistryArylchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCopper0104 chemical sciencesCatalysisSolventchemistry.chemical_compoundchemistryOrganic chemistryPalladiumChemistrySelect
researchProduct

Hydrophobic Encapsulated Phosphonium Salts-Synthesis of Weakly Coordinating Cations and their Application in Wittig Reactions

2015

Large and rigid tetraarylphosphonium tetrafluoroborate salts have been synthesized representing weakly coordinating cations with diameters of several nanometers. Divergent dendritic growth by means of thermal Diels-Alder cycloaddition was employed for the construction of the hydrophobic polyphenylene framework up to the third generation. X-ray crystal structure analysis of first-generation phosphonium tetrafluoroborate supported the rigidity of the non-collapsible shell around the phosphorus center and gave insight into solid-state packing and cation-anion distances. Copper(I)-catalyzed azide-alkyne ligation served as reliable method for the preparation of a first-generation triazolylphenyl…

Reaction conditionsTetrafluoroborateOrganic Chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureCopperCatalysisThird generationCycloadditionchemistry.chemical_compoundchemistryPolymer chemistryWittig reactionOrganic chemistryPhosphoniumChemistry - A European Journal
researchProduct