Search results for "Halide"

showing 10 items of 324 documents

Synthesis of Quinoline-Based Anion Receptors and Preliminary Anion Binding Studies with Selected Derivatives

2014

Six quinoline-based anion receptors were designed, prepared, and characterized, among which the crystal structure of an indole derivative was obtained. Selected receptors were tested for the recognition of halide anions in solution and showed some selectivity of chloride over bromide and iodide.

chemistry.chemical_classificationIndole testStereochemistryOrganic ChemistryIodideQuinolineHalideChlorideMedicinal chemistryCatalysischemistry.chemical_compoundchemistryBromidemedicineAnion bindingSelectivitymedicine.drugSynthesis
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Synthesis, characterization and thermal properties of small R2R′2N+X−-type quaternary ammonium halides

2005

Twenty-one R {sub 2} R {sup '} {sub 2}N{sup +} X {sup -} -type (R=methyl or ethyl, R {sup '}=alkyl, X=Br or I) quaternary ammonium (QA) halides have been prepared by using a novel one-pot synthetic route in which a formamide (dimethyl-, diethylformamide, etc.) is treated with alkyl halide in the presence of sodium or potassium carbonate. The formation of QA halides was verified with {sup 1}H-NMR, {sup 13}C-NMR, MS and elemental analysis. The crystal structures of four QA halides (two bromide and two iodide) were determined using X-ray single crystal diffraction, and the powder diffraction method was used to study the structural similarities between the single crystal and microcrystalline bu…

chemistry.chemical_classificationInorganic chemistryHalideCrystal structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryIonic liquidX-ray crystallographyMaterials ChemistryCeramics and CompositesMelting pointPhysical and Theoretical ChemistrySingle crystalAlkylPowder diffractionJournal of Solid State Chemistry
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Novel one-pot synthesis of quaternary ammonium halides: new route to ionic liquids

2004

Treatment of an amide with an alkyl or substituted alkyl halide in the presence of a weak base in a one-pot reaction leads to crystalline quaternary ammonium halides with reasonable chemical yields; some of the compounds show low melting points and a liquid range of over 50–100 °C before decomposition.

chemistry.chemical_classificationInorganic chemistryOne-pot synthesisHalideGeneral ChemistryCatalysischemistry.chemical_compoundchemistryAmideIonic liquidMaterials ChemistryMelting pointAmmoniumWeak baseAlkylNew Journal of Chemistry
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Chemical and spectroscopical evidence for an electron‐transfer mechanism in the reaction of arenesulfonyl chlorides with anions

1989

The reaction of amide and amidate anions 2 with p-toluenesulfonyl chloride (1) under different reaction conditions gives rise to the total or partial reduction of the acyl halide to p-toluenesulfinic acid (5) and acylation compounds in variable amounts depending on the crowding at the anionic center. This indicates that a Single-Electron Transfer (SET) mechanism is involved in the reactions of 1 with anions. Unpaired electron species are detected by ESR in the course of the reactions.

chemistry.chemical_classificationInorganic chemistrySulfonyl halideSulfinic acidChlorideInorganic ChemistryAcylationchemistry.chemical_compoundElectron transferchemistryUnpaired electronAmidePolymer chemistrymedicineAcyl halidemedicine.drugChemische Berichte
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An Easy Way Towardɛ-Caprolactone Macromonomers by Microwave Irradiation Using Early Lanthanide Halides as Catalysts

2002

Poly(e-caprolactone) macromonomers were synthesized under microwave irradiation from commercial caprolactone, using commercial hydrated lanthanide halides as catalysts. The molecular weight of the polymers was in the range 3 000–5 000. Higher molecular weights (5 000–20 000) and lower polydispersity indices were obtained with THF adducts of the lanthanide halides as catalysts and also by applying longer reaction times or using diethylene glycol as a coupling reagent.

chemistry.chemical_classificationLanthanideMaterials sciencePolymers and PlasticsOrganic ChemistryDispersityDiethylene glycolHalidePolymerMacromonomerRing-opening polymerizationchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCaprolactoneMacromolecular Rapid Communications
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The viscoelastic behavior of nylon 6/lithium halides mixtures

1980

Stress-relaxation experiments in the limit of small deformations have been carried out in a wide range of temperatures for pure nylon 6 and its mixtures with LiBr and/or LiCl. Master curves have been constructed, by allowing horizontal shifts only, showing the shape typical for semicrystalline polymers in the case of pure nylon and that of essentially amorphous polymers in the case of salted samples. The glass transition temperatures determined from the plot logaT− 1/T is increased when in the presence of salts. All such effects are considered to reflect the binding action of Li+ and Br− ions.

chemistry.chemical_classificationMaterials scienceAnalytical chemistryHalidechemistry.chemical_elementPolymerCondensed Matter PhysicsViscoelasticityAmorphous solidCrystallinitychemistry.chemical_compoundNylon 6chemistryOrganic chemistryGeneral Materials ScienceLithiumGlass transitionRheologica Acta
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Positron Annihilation in Alkali Halides at Low Temperatures

1986

We report on low-temperature positron studies for pure, single crystals of the alkali halides KCl, NaCl and NaF. Strong temperature dependences are observed in the lifetime and angular correlation measurements in the temperature range 10–300 K. Delocalized para-positronium is observed at low temperatures in the three crystals. The broadening, with rising temperature, of the narrow peak in the angular correlation curve can be accounted for by the self-trapping model of positronium. The results are discussed in the light of this model, in terms of positronium localization at imperfections and in terms of positron interactions with imperfections created in the spur of the positron. The increas…

chemistry.chemical_classificationMaterials scienceGeneral Physics and AstronomyHalideElectronAtmospheric temperature rangePositroniumDelocalized electronPositronchemistryPhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsPhysics::Chemical PhysicsAtomic physicsInorganic compoundSingle crystalJournal of the Physical Society of Japan
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The glass transition behaviour of salted nylon 6

1981

Glass transition measurements of nylon-6/lithium halides mixtures have been carried out in wide range of frequency with the aid of different experimental techniques. The results show an increase of the glass transition temperature when the salt is present and prove the larger effectiveness of lithium chloride with respect of lithium bromide. This effect, in line with the large reduction of the specific volume caused by the salt, is due to the formation of a pseudo-cross-linking between lithium ions and the carbonyl-oxygen groups of the polyamide.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsLithium bromideAnalytical chemistryHalideSalt (chemistry)chemistry.chemical_elementchemistry.chemical_compoundColloid and Surface ChemistryNylon 6chemistryPolyamideMaterials ChemistryLithium chlorideLithiumPhysical and Theoretical ChemistryComposite materialGlass transitionColloid and Polymer Science
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Fully Vacuum-Processed Wide Band Gap Mixed-Halide Perovskite Solar Cells

2017

Methylammonium lead mixed-halide perovskites MAPb(BrxI1–x)3 are promising materials for the preparation of tandem devices. When exposed to light, MAPb(BrxI1–x)3 segregates in iodide- and bromide-rich phases, limiting the achievable photovoltage and hence the attainable device efficiency. To date only solution-processed mixed-halide perovskites have been demonstrated. We present fully vacuum-deposited mixed-halide perovskite thin films with band gap of 1.72 and 1.87 eV, prepared by controlling the deposition rates of the different halide precursors. When used in thin-film devices, these materials lead to power conversion efficiencies of 15.9 and 10.5%, respectively, which are among the highe…

chemistry.chemical_classificationMaterials scienceTandemRenewable Energy Sustainability and the EnvironmentBand gapbusiness.industryIodideWide-bandgap semiconductorEnergy Engineering and Power TechnologyHalide02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesFuel TechnologychemistryChemistry (miscellaneous)Materials ChemistryOptoelectronicsThin film0210 nano-technologybusinessDeposition (law)Perovskite (structure)ACS Energy Letters
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Improved Preparations of Molybdenum Coordination Compounds from Tetrachlorobis(diethyl ether)molybdenum(IV)

2001

International audience; The reduction of MoCl5 with metallic tin in diethyl ether provides a rapid and convenient entry to [MoCl4(OEt2)2] This compound can be transformed easily and in high yields into a variety of other useful synthons. The loss of ether in the solid state affords a new and reactive form of MoCl4. Treatment with THF, PMe3 or LiOtBu affords [MoCl4(THF)2], [MoCl4(PMe3)3] or [Mo(OtBu)4] in high isolated yields. Treatment with metallic tin in THF affords [MoCl3(THF)3] All of these reactions can be carried out under simple experimental conditions and represent significant improvements relative to previously reported syntheses of the same compounds.

chemistry.chemical_classificationMolybdenumChemistrySynthonchemistry.chemical_elementHalideEtherMedicinal chemistry3. Good healthCoordination complexHalidesInorganic ChemistryMetalchemistry.chemical_compoundSynthetic methodsMolybdenumvisual_artvisual_art.visual_art_mediumOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryDiethyl etherTinReduction
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