Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Lowest triplet excited states of a novel heteroleptic iridium(III) complex and their role in the emission colour

2009

Abstract The [Ir(ppy-F 2 ) 2 Me 4 phen] +1 complex, where ppy-F 2 is 2-(2′,4′-fluorophenyl)pyridine and Me 4 phen is 3,4,7,8-tetramethyl-1,10-phenanthroline, has been theoretically investigated by means of DFT calculations. The molecular and electronic properties calculated for [Ir(ppy-F 2 ) 2 Me 4 phen] +1 are compared with those obtained for the simpler [Ir(ppy)(bpy)] +1 complex. The introduction of fluorine substituents in the ppy ligands and the use of phenanthroline instead of 2,2′-bipyridine as the diimine ligand increase the HOMO–LUMO energy gap and blue-shift the emission colour. The phenanthroline ligand causes the appearance of two nearly-degenerate LUMO orbitals of different symm…

Band gapChemistryLigandPhenanthrolinechemistry.chemical_elementCondensed Matter PhysicsPhotochemistryBiochemistryCrystallographychemistry.chemical_compoundExcited statePyridineIridiumPhysical and Theoretical ChemistryHOMO/LUMODiimineJournal of Molecular Structure: THEOCHEM
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Electron Transfer from Organic Aminophenyl Acid Sensitizers to Titanium Dioxide Nanoparticle Films

2009

Electron transfer from three conjugated amino-phenyl acid dyes to titanium and aluminum oxide nanocrystalline films was studied by using transient absorption spectroscopy with sub 20 fs time-resolution over the visible spectral region. All the dyes attached to TiO2 showed long-lived ground state bleach signals indicative of formation of new species. Global analysis of the transient kinetics of the dyes on TiO2 revealed stimulated emission decays of about 40 fs and less than 300 fs assigned to electron injection. The same dyes on Al2O3 substrates displayed long stimulated emission decays (ns) suggesting that electron transfer is blocked in this high band gap semiconductor. For two of the dye…

Band gapConjugated systemPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferGeneral EnergychemistryTitanium dioxideUltrafast laser spectroscopyDensity functional theoryStimulated emissionPhysical and Theoretical ChemistrySpectroscopyThe Journal of Physical Chemistry C
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A convenient route for the preparation of the monohydride catalyst trans-[RuCl(H)(dppe)2] (dppe=Ph2PCH2CH2PPh2): improved synthesis and crystal struc…

2013

Abstract A novel and improved room temperature synthesis of the monohydride catalyst trans-[RuCl(H)(dppe)2] complex (1, dppe (1,2-bis(diphenylphosphino)ethane) = Ph2PCH2CH2PPh2) proceeds through oxidation of methanol (the solvent) by the pentacoordinated cis-[RuCl(dppe)2][PF6] complex and t-BuOK as the base is described. Compound 1 was fully characterized by NMR (1H, 13C, 31P), ESI-MS(TOF +), FTIR and elemental analysis. The X-ray structure of 1 was reported for the first time and unambiguously confirms the trans-configuration of the complex.

Base (chemistry)chemistry.chemical_elementHomogeneous catalysisCrystal structure.PhotochemistryMedicinal chemistryRutheniumCatalysisInorganic Chemistrychemistry.chemical_compoundFaculdade de Ciências Exatas e da EngenhariaMaterials ChemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyta116Syntethic methdoschemistry.chemical_classificationChemistryHydridesHomogeneous catalisysX-ray crystal structureRutheniumSolventMethanolHydrogenation
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Influence of side chain characteristics on the aggregation-induced emission (AIE) properties of tetrasubstituted tetraphenylethylene (TPE)

2017

[EN] Five new tetraphenylethylene (TPE) derivatives were synthesised and their aggregation-induced emission (AIE) was evaluated in mixtures of THF/water and MeOH/water. The influence of regiochemistry and length of the chains in the substituents on emissive properties was studied.

BehaviorChemosensors010405 organic chemistryChemistryGeneral Chemical EngineeringSystemsRegioselectivityWaterGeneral ChemistryTetraphenylethylene010402 general chemistryPhotochemistry01 natural sciencesPolycarbazoles0104 chemical scienceschemistry.chemical_compoundCompostos orgànicsSide chainAggregation-induced emissionQuímica orgànicaDerivatives
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VOC's abatement: Photocatalytic oxidation of toluene in vapour phase on anatase TiO2 catalyst

1997

Publisher Summary The photocatalytic oxidation of toluene in the presence of water was performed in the gas–solid regime at room temperature by using TiO2. It has been found that the presence of water was beneficial to achieve the almost complete photo-oxidation of toluene to CO2 and H2O, in fact, only very small amounts of benzaldehyde vapor that is the main product of toluene partial oxidation, were detected. Volatile organic compounds, VOC's, are an important class of air pollutants usually found in the atmosphere of all urban and industrial areas. Toluene is one of these compounds, and because of its noxious nature several strategies have been identified to reduce its presence in indoor…

Benzaldehydechemistry.chemical_compoundAnatasechemistryBenzyl alcoholInorganic chemistryPhotocatalysisPartial oxidationPhotochemistryTolueneCatalysisBenzoic acid
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Photocatalytic degradation of toluene in aqueous suspensions of polycrystalline TiO2 in the presence of the surfactant tetradecyldimethylamino-oxide

2000

The heterogeneous photocatalytic method has been used for carrying out the toluene oxidation in synthetic aqueous solutions containing also a zwitterionic surfactant, i.e. tetradecyldimethylamino-oxide (C 14 DMAO). A batch photoreactor with immersed lamp and two kinds of polycrystalline TiO 2 catalysts were used. The results indicate a substantial increase of the toluene degradation rate in the presence of the surfactant; the complete photo- oxidation of toluene was achieved in a few hours of irradiation at the used experimental conditions; at higher irradiation times also C 14 DMAO was completely degraded. The main intermediates of toluene degradation were p-cresol (4-methyiphenol) and ben…

Benzaldehydechemistry.chemical_compoundMuconic acidchemistryHydroquinoneBenzyl alcoholPhotocatalysisPhotochemistryTolueneToluene oxidationBenzoic acid
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Highly Stable and Efficient Light-Emitting Electrochemical Cells Based on Cationic Iridium Complexes Bearing Arylazole Ancillary Ligands.

2017

A series of bis-cyclometalated iridium(III) complexes of general formula [Ir(ppy)2(N∧N)][PF6] (ppy− = 2-phenylpyridinate; N∧N = 2-(1H-imidazol-2-yl)pyridine (1), 2-(2-pyridyl)benzimidazole (2), 1-methyl-2-pyridin-2-yl- 1H-benzimidazole (3), 2-(4′-thiazolyl)benzimidazole (4), 1- methyl-2-(4′-thiazolyl)benzimidazole (5)) is reported, and their use as electroluminescent materials in light-emitting electrochemical cell (LEC) devices is investigated. [2][PF6] and [3][PF6] are orange emitters with intense unstructured emission around 590 nm in acetonitrile solution. [1][PF6], [4][PF6], and [5][PF6] are green weak emitters with structured emission bands peaking around 500 nm. The different photoph…

BenzimidazoleLigandchemistry.chemical_element02 engineering and technologyQuímica analíticaElectroluminescence010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPyridineIridiumChemistry AnalyticPhysical and Theoretical ChemistryTriplet state0210 nano-technologyAcetonitrileHOMO/LUMOInorganic chemistry
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Heterocyclic photorearrangements. Photochemical behaviour of some 3,5-disubstituted 1,2,4-oxadiazoles in methanol at 254 nm

1988

Photochemical behaviour of some 3,5-disubstituted 1,2,4-oxadiazoles in methanol at 254 nm has been investigated. Ring photoisomerization to the 1,3,4-oxadiazole heterocycle or formation of open chain compounds involving the nucleophilic solvent was shown to depend on the nature and the position of the substituent. Photoinduced ring closure into the benzimidazole system, involving a 3-N-phenylamino side chain sequence and a photolytic intermediate of the oxadiazole heterocycle, is also reported.

Benzimidazolechemistry.chemical_compoundNucleophilePhotoisomerizationchemistryBicyclic moleculeOrganic ChemistrySide chainSubstituentOxadiazoleRing (chemistry)PhotochemistryJournal of Heterocyclic Chemistry
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ChemInform Abstract: Heterocyclic Photorearrangements. Photochemical Behaviour of Some 3,5-Disubstituted 1,2,4-Oxadiazoles in Methanol at 254 nm.

1989

Photochemical behaviour of some 3,5-disubstituted 1,2,4-oxadiazoles in methanol at 254 nm has been investigated. Ring photoisomerization to the 1,3,4-oxadiazole heterocycle or formation of open chain compounds involving the nucleophilic solvent was shown to depend on the nature and the position of the substituent. Photoinduced ring closure into the benzimidazole system, involving a 3-N-phenylamino side chain sequence and a photolytic intermediate of the oxadiazole heterocycle, is also reported.

Benzimidazolechemistry.chemical_compoundPhotoisomerizationNucleophileChemistrySide chainSubstituentOxadiazoleGeneral MedicineMethanolRing (chemistry)PhotochemistryChemInform
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Photocatalytic oxidation mechanism of benzonitrile in aqueous suspensions of titanium dioxide

2007

Abstract The photocatalytic oxidation of benzonitrile was carried out in aqueous suspensions (pH 11) of commercial polycrystalline TiO 2 (Merck and Degussa P25) irradiated by ultraviolet light. The rate of decomposition was dependent on the concentration of benzonitrile and followed a pseudo-first order kinetics. The complete mineralization of a 0.70 mM benzonitrile solution was achieved in ca. 8 h by using TiO 2 Degussa P25, whereas the substrate was only partially mineralized even after 14 h of irradiation in the presence of TiO 2 Merck. The final oxidation products were carbonate and nitrate. The appearance and the evolution of organic and inorganic intermediate species were also investi…

Benzonitrilechemistry.chemical_compoundAqueous solutionchemistryTitanium dioxideUltraviolet lightPhotocatalysisSubstrate (chemistry)General ChemistryMineralization (soil science)PhotochemistryCatalysisCatalysisCatalysis Today
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