Search results for "Iodide"

showing 10 items of 405 documents

Micropolarity and Order in the Reverse Micelles of L62 and L64 Pluronic Copolymers, As Studied by Molecular Probe Techniques

1998

The reverse micelles of triblock copolymers poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) EO6PO36EO6 (Pluronic L62) and EO13PO30EO13 (Pluronic L64) in ternary (copolymer/o-xylene/water) and binary (copolymer/water) systems with different water contents were evidenced and investigated by fluorescence, absorption, and spin probe techniques. The spectral parameters of the polarity sensitive probes, 1-anilinonaphthalene-8-sulfonic acid (ANS), dansylhexadecylamine (Dansyl), pyrenesulfonic acid (PSA), 4-nitropyridine N-oxide (NP) and 4-(N,N‘-dimethyl-N-alkyl)ammonium 2,2‘,6,6‘-tetramethylpiperidine-1-oxyl iodide (CAT n), were related to the local hydration and polari…

chemistry.chemical_classificationEthylene oxideIodideAnalytical chemistryPoloxamerMicelleSurfaces Coatings and FilmsSpin probechemistry.chemical_compoundchemistryMaterials ChemistryCopolymerPropylene oxidePhysical and Theoretical ChemistryAbsorption (chemistry)The Journal of Physical Chemistry B
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Reversible stimulus-responsive Cu(i) iodide pyridine coordination polymer

2015

We present a structurally flexible copper–iodide–pyridine-based coordination polymer showing drastic variations in its electrical conductivity driven by temperature and sorption of acetic acid molecules. The dramatic effect on the electrical conductivity enables the fabrication of a simple and robust device for gas detection. X-ray diffraction studies and DFT calculations allow the rationalisation of these observations.

chemistry.chemical_classificationFabricationChemistryCoordination polymerIodideMetals and AlloysNanotechnologySorptionQuímicaGeneral ChemistryAcetic acidPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAcetic acidCopper iodide pyridine coordination polymerElectrical resistivity and conductivityPyridineMaterials ChemistryCeramics and CompositesMoleculeChemical Communications
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<title>Iodine and mercury resonance lamps and their spectrum in far UV</title>

2001

Electrodeless iodine, mercury iodide, and mercury radio- frequency discharge lamps have been made to provide effective sources of atomic spectra for analytical spectroscopy providing powerful resonance radiation of iodine and mercury in the 120-253 nm region. The lamps are required and can be used for spectral calibration, resonance absorption, and fluorescence detection techniques, for investigation of atomic characteristics (e.g., branching ratios) and other purposes where intense monochromatic spectra are needed. Production technology, development, and investigation of the UV and VUV emission are described.© (2001) COPYRIGHT SPIE--The International Society for Optical Engineering. Downlo…

chemistry.chemical_classificationGas-discharge lampAbsorption spectroscopybusiness.industryChemistryIodideAnalytical chemistrychemistry.chemical_elementFluorescenceFluorescence spectroscopySpectral linelaw.inventionMercury (element)lawOptoelectronicsbusinessSpectroscopySPIE Proceedings
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Iodine and mercury resonance lamps for kinetics experiments and their spectra in the far ultraviolet

2000

Electrodeless iodine and mercury iodide radio-frequency discharge lamps have been made to provide intense sources of resonance radiation of iodine and mercury in the 183-253 nm region. Production technology and emission spectra in the ultraviolet and vacuum ultraviolet regions are described. Both lamps (iodine and mercury iodide) are designed and used for monitoring the iodine 2P1/2 (206.163 nm) and 2P3/2 (183.038 nm) level population kinetics after flash photolysis of I2 or other precursor molecules in laboratory experiments. The technique is suitable for the investigation of the gas phase reaction kinetics following the photolysis of I2 in the presence of O3.

chemistry.chemical_classificationGas-discharge lampAcoustics and UltrasonicsKineticsPhotodissociationIodideAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsIodinemedicine.disease_causeSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionMercury (element)chemistrylawmedicineFlash photolysisUltravioletJournal of Physics D: Applied Physics
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Photoresponsive ionic liquid crystals assembled: Via halogen bond: En route towards light-controllable ion transporters

2017

We demonstrate that halogen bonding (XB) can offer a novel approach for the construction of photoresponsive ionic liquid crystals. In particular, we assembled two new supramolecular complexes based on 1-ethyl-3-methylimidazolium iodides and azobenzene derivatives containing an iodotetrafluoro-benzene ring as XB donor, where the iodide anion acted as an XB acceptor. DSC and X-ray diffraction analyses revealed that the preferred stoichiometry between the XB donors and acceptors is 2 : 1, and that the iodide anions act as bidentate XB-acceptors, binding two azobenzene derivatives. Due to the high directionality of the XB, calamitic superanions are obtained, while the segregation occurring betw…

chemistry.chemical_classificationHalogen bondta114ChemistryInorganic chemistryIodideSupramolecular chemistryIonic bonding02 engineering and technologySupramolecular Chemistry Liquid Crystals Halogen Bonding Photoresponsive010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAcceptor0104 chemical sciencesCrystallographychemistry.chemical_compoundAzobenzeneIonic liquidMoleculeSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical Chemistry0210 nano-technology
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The Synergetic Interplay of Weak Interactions in the Ion-Pair Recognition of Quaternary and Diquaternary Ammonium Salts by Halogenated Resorcinarenes

2013

The influence of halogens on the noncovalent interactions of different upper-rim-substituted hexylresorcinarenes with quaternary and diquaternary ammonium iodide salts was investigated in the gas phase by electrospray ionization Fourier-transform ion-cyclotron-resonance (ESI-FTICR) mass spectrometry and in solution by 1H NMR titration studies. The electronic nature of the substituents on the upper rim of the resorcinarene was directly reflected in the order of binding strengths of the hosts towards quaternary and diquaternary ammonium cations in the gas phase. In solution, the opposite trend was observed, with generally higher binding constants for the diquaternary over the quaternary salts…

chemistry.chemical_classificationHydrogen bondElectrospray ionizationOrganic ChemistryInorganic chemistryResorcinareneAmmonium iodidechemistry.chemical_compoundchemistryComputational chemistryHalogenProton NMRNon-covalent interactionsAmmoniumPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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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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Mixed Iodide-Bromide Methylammonium Lead Perovskite-based Diodes for Light Emission and Photovoltaics.

2015

Vacuum deposition techniques are used to prepare mixed iodide–bromide methylammonium lead perovskite diodes via an intermediate double layer of the pure iodide and bromide perovskites. The diodes lead to bright electroluminescence, whose emission spectra maxima shift from the infrared toward the visible with increasing bromide content. When illuminated with AM1.5 simulated sunlight the devices function as efficient solar cells with power conversion efficiencies as high as 12.9%.

chemistry.chemical_classificationInfraredbusiness.industryIodideElectroluminescencechemistry.chemical_compoundchemistryPhotovoltaicsBromideOptoelectronicsGeneral Materials ScienceLight emissionPhysical and Theoretical ChemistrybusinessDiodePerovskite (structure)The journal of physical chemistry letters
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4-[4-(4-Fluoro-phen-yl)-2-methyl-5-oxo-2,5-dihydro-isoxazol-3-yl]-1-methyl-pyridinium iodide-4-[3-(4-fluoro-phen-yl)-2-methyl-5-oxo-2,5-dihydro-isoxa…

2007

The crystal structure of the title compound, C(16)H(16)FN(2)O(2) (+)·I(-), was determined as part of a study of the biological activity of isoxazolone derivatives as p38 mitogen-activated protein kinase (MAPK) inhibitors. The X-ray crystal structure of 4-[4-(4-fluoro-phenyl)-2-methyl-5-oxo-2,5-dihydro-isoxazol-3-yl]-1-methyl-pyridinium iodide showed the presence of the regioisomer 4-[3-(4-fluoro-phenyl)-2-methyl-5-oxo-2,5-dihydro-isoxazol-4-yl]-1-methyl-pyridinium iodide. The synthesis of the former compound was achieved by reacting 4-(4-fluoro-phenyl)-3-(4-pyridyl)isoxazol-5(2H)-one after treatment with Et(3)N in dimethyl-formamide, with iodo-methane. The unexpected formation of the regioi…

chemistry.chemical_classificationIodideBiological activityGeneral ChemistryCrystal structureDihedral angleAziridineCondensed Matter PhysicsBioinformaticsMedicinal chemistryOrganic Paperschemistry.chemical_compoundchemistryStructural isomerGeneral Materials SciencePyridiniumAfter treatmentActa crystallographica. Section E, Structure reports online
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Experimental and theoretical investigations of the redox behavior of the heterodichalcogenido ligands [(EP(i)Pr2)(TeP(i)Pr2)N](-) (E = S, Se): cyclic…

2008

The two-electron oxidation of the lithium salts of the heterodichalcogenidoimidodiphosphinate anions [(EP (i)Pr 2)(TeP (i)Pr 2)N] (-) ( 1a, E = S; 1b, E = Se) with iodine yields cyclic cations [(EP (i)Pr 2)(TeP (i)Pr 2)N] (+) as their iodide salts [(SP (i)Pr 2)(TeP (i)Pr 2)N]I ( 2a) and [(SeP (i)Pr 2)(TeP (i)Pr 2)N]I ( 2b). The five-membered rings in 2a and 2b both display an elongated E-Te bond as a consequence of an interaction between tellurium and the iodide anion. One-electron reduction of 2a and 2b with cobaltocene produces the neutral dimers (EP (i)Pr 2NP (i)Pr 2Te-) 2 ( 3a, E = S; 3b, E = Se), which are connected exclusively through a Te-Te bond. Two-electron reduction of 2a and 2b …

chemistry.chemical_classificationIodideInorganic chemistryCrystal structureNuclear magnetic resonance spectroscopyCoordination complexInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryCobaltoceneStructural isomerDensity functional theoryPhysical and Theoretical ChemistryHOMO/LUMOInorganic chemistry
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