Search results for "Bonding"

showing 10 items of 996 documents

A Supramolecularly-Caged Ionic Iridium(III) Complex Yielding Bright and Very Stable Solid-State Light-Emitting Electrochemical Cells

2008

A new iridium(III) complex showing intramolecular interligand pi-stacking has been synthesized and used to improve the stability of single-component, solid-state light-emitting electrochemical cell (LEC) devices. The pi-stacking results in the formation of a very stable supramolecularly caged complex. LECs using this complex show extraordinary stabilities (estimated lifetime of 600 h) and luminance values (average luminance of 230 cd m-2) indicating the path toward stable ionic complexes for use in LECs reaching stabilities required for practical applications.

Analytical chemistrySolid-statechemistry.chemical_elementIonic bondingGeneral ChemistryPhotochemistryBiochemistryLuminanceCatalysisElectrochemical cellColloid and Surface ChemistrychemistryIntramolecular forceIridiumJournal of the American Chemical Society
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Effect of the addition of different doping agents on visible light activity of porous TiO2 photocatalysts

2018

Abstract The influence of the addition of different doping agents (N, W and Hf) on the macroporous TiO2 photoactivity toward the Rhodamine B degradation and ethanol photo-oxidation was evaluated. The samples were characterized by XRD, XPS, SEM, TEM, N2 adsorption-desorption, UV–vis Diffuse Reflectance and Photoluminescence spectroscopies to study also the changes in the physico-chemical properties due to the presence of dopants. The photonic effect and the high ordered porous structure of the macroporous TiO2 that lead to increase the path length of the light, were the key factors that allow to enhance the catalytic activity towards the dye and VOC degradation under visible and solar light …

AnataseMaterials sciencePhotoluminescenceIonic bondingVOCs remediation02 engineering and technology010402 general chemistry01 natural sciencesCatalysisCatalysichemistry.chemical_compoundPhotocatalysiRhodamine BPhysical and Theoretical ChemistryWater purificationDopantInverse opal materialProcess Chemistry and TechnologyDoping021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringTitanium dioxideSettore CHIM/07 - Fondamenti Chimici Delle TecnologieDiffuse reflection0210 nano-technologyVisible spectrumMolecular Catalysis
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Highlights on contemporary recognition and sensing of fluoride anion in solution and in the solid state

2012

The fluoride anion has recently gained well deserved attention among the scientific community for its importance in many fields of human activities, but also for concerns on its effect on health and the environment. Although surprisingly overlooked in systematic studies in the past, fluoride has nowadays become a topical target in the field of anion recognition. A multitude of scientific reports are published every year where the establishment of efficient and specific interaction with fluoride is sought in polar and aqueous media. Here, the emphasis is directed to a detailed description of the most interesting contemporary studies in the field, with a particular focus given to those publis…

AnionsAqueous mediumChemistryMultitudeSolid-stateMolecular ConformationWaterNanotechnologyHydrogen BondingGeneral ChemistryCrystallography X-RaySolutionschemistry.chemical_compoundFluoridesHumansEngineering ethicsFluorideta116Chemical Society Reviews
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From attraction to repulsion : anion–π interactions between bromide and fluorinated phenyl groups

2011

Anion–π interactions in crystals of fluorobenzyl ammonium salts depend on the degree of fluorination at the aromatics.

AnionsBromidesBenzylaminesHalogenationInorganic chemistryMolecular ConformationChemieElectronsCrystallography X-RayCatalysisPiperazinesDegree (temperature)Ionchemistry.chemical_compoundBromidePolymer chemistryMaterials ChemistryAmmoniumMetals and AlloysHydrogen BondingGeneral ChemistryAttractionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFluorobenzenesQuaternary Ammonium CompoundschemistryCeramics and Composites
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Cooperativity of H-bonding and anion–π interaction in the binding of anions with neutral π-acceptors

2012

A rare anion-π complex between bromide and a neutral receptor is reported and related receptor systems are studied with a series of anions. The interaction is observed in the solid state and in solution, and further evidence for it is obtained by a computational study.

AnionsBromidesModels MolecularMagnetic Resonance SpectroscopyChemistryHydrogen bondInorganic chemistryChemieMolecular ConformationMetals and AlloysSolid-stateHydrogen BondingCooperativityGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographychemistry.chemical_compoundBromideBenzamidesMaterials ChemistryCeramics and Compositesta116Chemical Communications
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Self-assembly of 3,5-bis(ethoxycarbonyl)pyrazolate anions and ammonium cations of β-phenylethylamine or homoveratrylamine into hetero-double-stranded…

2009

Hydrogen-bonded double-stranded hetero-helices are formed when reacting sodium 3,5-bis(ethoxycarbonyl)pyrazolate with beta-phenethylammonium or homoveratrylammonium chloride, in which one of the strands is defined by the ammonium cations and the other one by the pyrazolate anions.

AnionsCircular DichroismSodiumOrganic Chemistrychemistry.chemical_elementHydrogen BondingCrystallography X-RayBiochemistryChlorideProtein Structure SecondaryQuaternary Ammonium Compoundschemistry.chemical_compoundchemistryPhenethylaminesPolymer chemistrymedicineOrganic chemistryAmmoniumSelf-assemblyBeta-PhenylethylaminePhysical and Theoretical ChemistryDouble strandedmedicine.drugOrganic & Biomolecular Chemistry
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CH-Directed Anion-π Interactions in the Crystals of Pentafluorobenzyl-Substituted Ammonium and Pyridinium Salts

2010

Simple pentafluorobenzyl-substituted ammonium and pyridinium salts with different anions can be easily obtained by treatment of the parent amine or pyridine with the respective pentafluorobenzyl halide. Hexafluorophosphate is introduced as the anion by salt metathesis. In the case of the ammonium salt 4, water co-crystallisation seems to suppress effective anion-pi interactions of bromide with the electron-deficient aromatic system, whereas with salts 5 and 6 such interactions are observed despite the presence of water. However, due to asymmetric hydrogen-bonding interactions with ammonium side chains, the anion of 5 is located close to the rim of the pentafluorophenyl group (eta(1) interac…

AnionsHydrocarbons FluorinatedInorganic chemistryChemieMolecular ConformationSalt (chemistry)Pyridinium CompoundsCrystallography X-RayMedicinal chemistryCatalysischemistry.chemical_compoundBromideHexafluorophosphatePyridineAmmoniumPi interactionchemistry.chemical_classificationMolecular StructureChemistryHydrogen bondOrganic ChemistryHydrogen BondingGeneral ChemistryCarbonQuaternary Ammonium CompoundsModels ChemicalSaltsPyridiniumChemistry - A European Journal
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New anionic cobalt complexes using highly hindered bis-amides with varying donor abilities as ligands.

2007

Four potential tetradentate ligands of formulae 1,2-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)ethane (H(4)L(1), 1), 1,2-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)propane (H(4)L(2), 2), 1,2-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)benzene (H(4)L(3), 3) and 1,8-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)naphthalene (H(4)L(4), 4) have been prepared and the crystal structures of three of them (1, 3 and 4) determined by single crystal X-ray diffraction. The investigation of their complexing ability toward Co(II) afforded the compounds of formulae [Co(III)(L(3))Na(I)(H(2)O)(2)] (5), [Co(III)(L(n))Li(I)(H(2)O)2] with n = 1 (6), 2 (7) and 3 (8) and [Co(II)(L(4))Li(I)(2)] (9). Complexes 5-8 are squa…

AnionsMagnetic Resonance SpectroscopyMolecular StructureHydrogen bondStereochemistryLigandSpectrochemical seriesTemperaturechemistry.chemical_elementHydrogen BondingNuclear magnetic resonance spectroscopyCrystal structureCobaltCrystallography X-RayLigandsAmidesInorganic ChemistryCrystallographyMagneticsDeprotonationchemistryOrganometallic CompoundsCobaltSingle crystalDalton transactions (Cambridge, England : 2003)
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Polyfunctional recognition of pyridinedicarboxylate anions with macrocyclic polyamine receptors containing heteroaromatic groups.

2008

The interaction of the biologically relevant anions deriving from the six pyridinedicarboxylic acids (H2PDC) with two macrocyclic receptors containing a pentamine chain and a bipyridine (1) or a phenanthroline (2) moiety, as well as with the aliphatic analogue [21]aneN7 (3), was studied by means of spectroscopic methods (UV-vis, NMR) and potentiometric titrations affording the stability constants of the adducts formed. All three receptors form stable complexes with the substrates thanks to the formation of several salt bridges and hydrogen bond contacts, as observed in the crystal structure of the H8[3(2,6-PDC)4] x H2O x 0.5 EtOH solid compound. Additional pi-stacking interactions between t…

AnionsModels MolecularMacrocyclic CompoundsStereochemistryPyridinesPhenanthrolineStatic ElectricityCarboxylic AcidsHydrocarbons Aromaticchemistry.chemical_compoundBipyridineMolecular recognitionPolymer chemistryPolyaminesMoietychemistry.chemical_classificationBinding SitesHydrogen bondSpectrum AnalysisOrganic ChemistryHydrogen BondingDicarboxylic acidchemistryStability constants of complexesPotentiometryAliphatic compoundThe Journal of organic chemistry
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A highly enantioselective abiotic receptor for malate dianion in aqueous solution

2006

The highly enantioselective molecular recognition of the malate dianion by a synthetic receptor in aqueous solution has been studied by potentiometric titrations, mass spectrometry (ESI-MS), diffusion measurements (PGSE NMR) and molecular modeling. Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es

AnionsModels MolecularMalate dianionSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyMolecular modelUNESCO::QUÍMICADiffusionPotentiometric titrationMalatesMolecular modelingAbiotic receptorMass spectrometry:QUÍMICA [UNESCO]CatalysisSubstrate SpecificityMolecular recognitionComputational chemistryMaterials ChemistryOrganic chemistryAqueous solutionReceptorAbiotic componentEnantioselectiveAqueous solutionMolecular StructureChemistrySpectrometryMeasurementsMetals and AlloysEnantioselective synthesisWaterHydrogen BondingStereoisomerismGeneral ChemistryGeneral MedicineUNESCO::QUÍMICA::Química macromolecularCombinatorial chemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolutionsCeramics and CompositesPotentiometryEnantioselective ; Abiotic receptor ; Malate dianion ; Aqueous solution ; Spectrometry ; Measurements ; Molecular modeling:QUÍMICA::Química macromolecular [UNESCO]
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