Search results for "naphthalene"

showing 10 items of 267 documents

Specific interaction of citrate with bis(fluorophoric) bibrachial lariat aza-crown in comparison with the other components of the Krebs cycle

2006

Clares Garcia, M. Paz, M.Paz.Clares@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es ; Soriano Soto, Concepcion, Concepcion.Soriano@uv.es ; Tejero Toquero, Roberto, Roberto.Tejero@uv.es

Citrate ; Krebs cycle ; Fluorescence ; NaphthaleneUNESCO::QUÍMICACrown (botany)UNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryFluorescenceMedicinal chemistry:QUÍMICA [UNESCO]CatalysisFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCitric acid cyclechemistry.chemical_compoundchemistryBiochemistryMaterials ChemistryCeramics and Composites:QUÍMICA::Química analítica [UNESCO]CitrateKrebs cycleThe Krebs CycleNaphthaleneNaphthalene
researchProduct

(Z)-4-(2-Naphthylamino)pent-3-en-2-one

2011

The title compound, C15H15NO, which was synthesized under solvent-free conditions by the reaction of acetoacetone and 2-naphthylamine, adopts a Z conformation about the C=C bond. The enamine–ketone fragment is approximately planar [maximum deviation = 0.026 (3) Å] and forms a dihedral angle of 39.78 (3)° with the naphthalene ring system. An intramolecular N—H...O hydrogen bond is observed.

CrystallographyHydrogen bondMaximum deviationGeneral ChemistryDihedral angleCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic Paperschemistry.chemical_compoundCrystallographychemistryQD901-999General Materials ScienceNaphthaleneActa Crystallographica Section E
researchProduct

Partitioning study of polycyclic aromatic hydrocarbons between water and some selected water-insoluble phases

2007

An investigation on the partitioning of naphthalene and phenanthrene between water and some water-insoluble phases has been carried out by Uv-vis-NIR spectrophotometry. The analysis of the experimental results emphasized the role of intermolecular interactions and structural features of the hosting phases as driving forces of the partitioning of these polycyclic aromatic hydrocarbons. The critical comparison of the resulting distribution constants allowed to evaluate the potentials of some extracting phases to set up sensitive analytical methods and/or effective environment remediation technologies.

DNA-ADDUCTSEXTRACTIONSpectroscopy Near-Infraredmedicine.diagnostic_testEnvironmental remediationChemistryMUTATIONSIntermolecular forcetechnology industry and agricultureWaterWater insolublePhenanthreneSensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundSolubilityEnvironmental chemistrySpectrophotometrySOLUBILIZATIONmedicinePolycyclic CompoundsSpectrophotometry UltravioletGeneral Environmental ScienceNaphthalene
researchProduct

DNA binding, nuclease activity, DNA photocleavage and cytotoxic properties of Cu(II) complexes of N-substituted sulfonamides.

2013

Abstract Ternary copper(II) complexes [Cu(NST)2(phen)] (1) and [Cu(NST)2(NH3)2]·H2O (2) [HNST = N-(4,5-dimethylthiazol-2-yl)naphthalene-1-sulfonamide] were prepared and characterized by physico-chemical techniques. Both 1 and 2 were structurally characterized by X-ray crystallography. The crystal structures show the presence of a distorted square planar CuN4 geometry in which the deprotonated sulfonamide, acting as monodentate ligand, binds to the metal ion through the thiazole N atom. Both complexes present intermolecular π–π stacking interactions between phenanthroline rings (compound 1) and between naphthalene rings (compound 2). The interaction of the complexes with CT DNA was studied b…

DenticityStereochemistryCell SurvivalUltraviolet RaysPhenanthrolineRadicalStackingAscorbic AcidNaphthalenesBiochemistryFluorescence spectroscopyInorganic Chemistrychemistry.chemical_compoundInhibitory Concentration 50Coordination ComplexesCell Line TumorAnimalsHumansDNA CleavageThiazoleNucleaseSulfonamidesBinding SitesbiologyCytotoxinsHydroxyl RadicalDNAHydrogen PeroxidePhotochemical ProcessesKineticschemistrybiology.proteinCattleDNACopperPhenanthrolinesJournal of inorganic biochemistry
researchProduct

Theoretical study on hydration of two particular diazanaphthalenes

2005

Abstract Cinnoline (1) and Phthalazine (2), diazanaphthalenes involved in certain biological reactions, have been studied computational with the purpose of comparing their protonation and covalent hydration mechanisms. Geometry optimizations of neutral, mono- and di-protonated cations and hydrated products were performed at HF, DFT/B3LYP levels of theory using 6-311G* basis set and single points energies were calculated at the MP2 level of theory using the same basis set. In agreement with experimental results, calculations predict a two-step mechanism resulting in a hydrated cation in which the OH of the water is located depending on the position of both nitrogen in the diazanaphthalene mo…

DiazanaphthaleneProtonationCondensed Matter PhysicsEnergy minimizationBiochemistrychemistry.chemical_compoundchemistryComputational chemistryCovalent bondMoleculePhysical and Theoretical ChemistryPhthalazineCinnolineBasis setJournal of Molecular Structure: THEOCHEM
researchProduct

Perfluoro-1,1′-biphenyl and perfluoronaphthalene and their derivatives as π-acceptors for anions

2015

Addition of anions to perfluorinated 1,1′-biphenyl 1 or naphthalene 2 results in a shift of the 19F NMR signals. However, any specific interaction cannot be assigned to this effect. In order to study the interaction in more detail, the salt derivatives 3 and 4 were prepared and studied by single crystal X-ray diffraction revealing weak anion–π interactions in the solid state.

Diffractionchemistry.chemical_classificationBiphenylanion-pi interactionsSolid-stateSalt (chemistry)General ChemistryFluorine-19 NMRCatalysisIonCrystallographychemistry.chemical_compoundchemistryMaterials ChemistryOrganic chemistryta116Single crystalNaphthaleneNew Journal of Chemistry
researchProduct

Two atropisomers of tricarbonyl[η6-7-chloro-3-(3-chloro-2-methylphenyl)-2,4,8-trimethyl-1,2,3,4-tetrahydro-2,4-dibora-1,3-diazanaphthalene]chromium(0)

2001

The structures of two atropisomers of the title compound, [Cr(C16H18B2Cl2N2)(CO)3], are reported. For both compounds, the Cr(CO)3 moiety is bound to the C6 aromatic ring of the mol­ecule; the existence of atropisomers resulting from the non-equivalence of both faces of the C6 aromatic ring is a consequence of the 3-chloro-2-methylphenyl ring being nearly perpendicular to the mean plane of the 2,4-dibora-1,3-di­aza­naphthalene ring. The orientation of the Cr(CO)3 tripod relative to the C6 aromatic ring is such that it is nearly eclipsed in one isomer (2.4° rotation from being eclipsed with C—N, C—Cl and C—H) and slightly twisted (16.2°) from an eclipsed conformation in the other.

Eclipsed conformationAtropisomerbiologyBicyclic moleculeStereochemistryChemistryGeneral MedicineCrystal structurebiology.organism_classificationMedicinal chemistryGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundTetraMoleculeMoietyNaphthaleneActa Crystallographica Section C Crystal Structure Communications
researchProduct

Twofold Electrochemical Amination of Naphthalene and Related Arenes

2017

The twofold, electrochemical amination reaction of polycyclic arenes, e.g. naphthalene (4), via Zincke intermediates is demonstrated for the first time. The installation of the nitrogen functionalities occurs regioselectively in positions 1 and 5 of naphthalene (4). The key for this electro-conversion is boron-doped diamond as anode material. The method of the multi-amination reaction is expanded to other aromatic substrates. A detailed study is provided, covering electrolysis parameters, e.g. anode material, electrolyte system, current density, separator, etc. Despite the moderate yields, this approach offers the first direct electro-synthetic access to diaminated products.

Electrolysis010405 organic chemistryChemistryInorganic chemistryDiamondElectrolyteengineering.material010402 general chemistryElectrochemistry01 natural sciencesCatalysis0104 chemical sciencesAnodelaw.inventionchemistry.chemical_compoundlawElectrochemistryengineeringAminationSeparator (electricity)NaphthaleneChemElectroChem
researchProduct

From monolayer to multilayer N-channel polymeric field-effect transistors with precise conformational order

2012

Monolayer field-effect transistors based on a high-mobility n-type polymer are demonstrated. The accurate control of the long-range order by Langmuir-Schafer (LS) deposition yields dense polymer packing exhibiting good injection properties, relevant current on/off ratio and carrier mobility in a staggered configuration. Layer-by-layer LS film transistors of increasing thickness are fabricated and their performance compared to those of spin-coated films.

Electron mobilityMaterials scienceTransistors ElectronicPolymersNanotechnologyThiophenesNaphthalenesTransistorslaw.inventionlawMonolayerElectronicDeposition (phase transition)General Materials Sciencemonolayer field-effect transistorchemistry.chemical_classificationbusiness.industrysemiconducting polymersMechanical EngineeringTransistorTransistor monolayer polymers orderPolymercharge transportchemistrylayered materialsMechanics of MaterialsN channelOptoelectronicsField-effect transistorbusiness
researchProduct

Poly(naphthalenediimidequaterthiophene):Poly(hexyilthiophene) Heterojunctions. Efficient Polymer-to-Polymer Electron Transfer Interfaces

2013

Organic thin films solar cells and plastic solar cells [1] have attracted the attention of the scientific community especially as regards the performance of new conjugated polymers including their interfaces [2-4]. In this work, poly(naphthalenediimidequaterthiophene) (PNDIT4) and poly(hexyilthiophene) (P3HT) have been employed, for the first time, for engineering planar and bulk heterojunctions by the synergetic use of two techniques: electropolymerization and layer by layer deposition. Electropolymerization has been used for obtaining PNDIT4 thin films on transparent ITO/PET electrodes, starting from the synthesized monomer. Inverse Langmuir-Schaefer technique has been employed for deposi…

Electron transfer poly(naphthalenediimidequaterthiophene)Settore CHIM/02 - Chimica Fisica
researchProduct