Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Enhanced flow-injection–chemiluminometric determination of sulphonamides by on-line photochemical reaction

2003

Abstract The viability of the tandem photochemical reaction-chemiluminescence detection has been studied for an heterogeneous group of sulphonamides (sulphamethoxazole, sulphadiazine, sulphamerazine, sulphamethoxypyridazine, sulphacetamide, sulphadimidine, sulphanilamide, sulphathiazole and sulphaguanidine) using sulphamethoxazole (whose chemiluminescent behaviour has not been previously reported) as a test substance. The ‘on-line’ photochemical-reaction of sulphonamides provides an enhancing influence on the chemiluminometric response of the drugs during their oxidation by potassium permanganate in sulphuric acid medium (sulphamethoxazole, sulphacetamide, sulphadimidine and sulphanilamide …

Detection limitChromatographyFluorescence spectrometryPhotochemistryBiochemistryOrders of magnitude (mass)Analytical Chemistrylaw.inventionStandard curvePotassium permanganatechemistry.chemical_compoundchemistrylawSulphaguanidineEnvironmental ChemistryPhotodegradationSpectroscopyChemiluminescenceAnalytica Chimica Acta
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A conjugated polymer with ethyl 2-(2-(pyridin-2-yl)-1H-benzo[d]imidazol-1-yl) acetate units as a novel fluorescent chemosensor for silver(I) detection

2013

Abstract A novel conjugated polymer ( P1 ) containing fluorene and ethyl 2-(2-(pyridin-2-yl)-1 H -benzo[ d ]imidazol-1-yl)acetate (PBMA) was designed and successfully synthesized through the Sonogashira coupling reaction. P1 shows high sensitivity and selectivity for Ag + detection in comparison to other metal cations. Upon addition of Ag + , the fluorescent emission of the polymer solution in THF was quenched dramatically, accompanying the color changed from blue to green. The detection limit for Ag + was 5 × 10 −8  mol L −1 . However, the similar copolymers P2 and P3 containing 2-(pyridin-2-yl)-1 H -benzo[ d ]imidazole and 2-(thiophen-2-yl)-1 H -benzo[ d ]imidazole, respectively, did not …

Detection limitMetals and AlloysSonogashira couplingFluoreneConjugated systemCondensed Matter PhysicsPhotochemistryFluorescenceMedicinal chemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMaterials ChemistryProton NMRImidazoleElectrical and Electronic EngineeringSelectivityInstrumentationSensors and Actuators B: Chemical
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Boron-Doped Diamond Electrodes for Electroorganic Chemistry

2011

Boron-doped diamond (BDD) electrodes provide an unusually wide electrochemical window in protic media, since there exist large offset potentials for the evolution of molecular hydrogen and oxygen, respectively. At the anode, alcohols are specifically converted to alkoxyl radicals. These can be used for chemical synthesis. When the enormous reactivity of such intermediate spin centers is not controlled, mineralization or electrochemical incineration dominates. Efficient strategies include either high substrate concentrations or fluorinated alcohols which seem to stabilize the spin centers in the course of reaction.

Diamondchemistry.chemical_elementengineering.materialElectrosynthesisPhotochemistryElectrochemistryCathodelaw.inventionAnodechemistrylawElectrodeengineeringBoronElectrochemical window
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The importance of a highly active and DeltapH-regulated diatoxanthin epoxidase for the regulation of the PS II antenna function in diadinoxanthin cyc…

2005

The present study focuses on the regulation of diatoxanthin (Dtx) epoxidation in the diadinoxanthin (Ddx) cycle containing algae Phaeodactylum tricornutum, Thalassiosira pseudonana, Cyclotella meneghiniana and Prymnesium parvum and its significance for the control of the photosystem II (PS II) antenna function. Our data show that Dtx epoxidase can exhibit extremely high activities when algal cells are transferred from high light (HL) to low light (LL). Under HL conditions, Dtx epoxidation is strongly inhibited by the light-driven proton gradient. Uncoupling of the cells during HL illumination restores the high epoxidation rates observed during LL. In Ddx cycle containing algae, non-photoche…

DiatomsPhotosystem IIbiologyLightPhysiologyZeaxanthin epoxidaseAlgal ProteinsDiadinoxanthinDiatoxanthinEukaryotaPhotosystem II Protein ComplexPlant ScienceHydrogen-Ion ConcentrationXanthophyllsPhotochemistrychemistry.chemical_compoundchemistryPhotoprotectionbiology.proteinElectrochemical gradientChlorella vulgarisOxidoreductasesAgronomy and Crop ScienceChlorophyll fluorescenceViolaxanthinJournal of plant physiology
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The influence of substitution in the quinoxaline nucleus on 1,3-dipolar cycloaddition reactions: A DFT study

2013

Abstract The reaction mechanism of 1,3-dipolar cycloadditions of both symmetric and unsymmetric benzo-condensed diazines with a nitrilimine dipole, to give two different mono- and bis-cycloadducts, in tetrahydrofuran (THF) solution, was studied by DFT calculations. The results obtained show that each 1,3-dipolar cycloaddition reaction always proceeds by a two steps mechanism, in which the first intermediate shows only one covalent bond between the beta carbon of the nitrilimine and the aromatic nitrogen of the diazine molecule. The structure and energy content of the two transition states of the two cycloaddition steps, in the case of the unsymmetric benzo-condensed diazine, nicely explains…

DiazineReaction mechanismNitrilimineCondensed Matter PhysicsPhotochemistryBiochemistryCycloadditionTransition statechemistry.chemical_compoundQuinoxalinechemistryComputational chemistry13-Dipolar cycloadditionMoleculePhysical and Theoretical ChemistryComputational and Theoretical Chemistry
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Efficient Nucleophilic Degradation of an Organophosphorus Pesticide “Diazinon” Mediated by Green Solvents and Microwave Heating

2019

An efficient strategy for the degradation of organophosphate pesticide Diazinon was investigated. In this work, ionic liquids, bio-based solvents, and two conventional organic solvents were used as reaction media. Kinetics studies by means of half-life (t1/2,h) were followed by 31P NMR and the products analyzed by GC-MS, HPLC-MS and NMR techniques. These results have shown that t1/2 values in ionic liquids were the lowest and also they were able to activate two electrophilic centers in Diazinon, whilst degradation in bio-based solvents occurred slowly by only an aromatic pathway. In addition, a study to estimate the influence of green activation techniques was carried out by using Ultrasoun…

DiazinonKinetics02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesmicrowaveslcsh:Chemistryionic liquidschemistry.chemical_compoundNucleophile31P NMRorganophosphate pesticidesOriginal ResearchultrasoundGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSolventChemistrylcsh:QD1-999chemistrygreener solventsIonic liquidDegradation (geology)Piperidine0210 nano-technologyMicrowaveFrontiers in Chemistry
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Mechanistic details of the domino reaction of nitronaphthalenes with the electron-rich dienes. A DFT study

2008

Abstract The reaction of 1-nitronaphthalene ( 1 ) with the Danishefsky diene ( 2 ) to give the dihydrophenanthrene derivative 11 has been theoretically studied using DFT methods. This reaction is a domino process that is initialized by a polar Diels–Alder reaction between 1 and 2 to give the formally [2 + 4] cycloadduct 3 . The subsequent concerted elimination of nitrous acid ( 4 ) from 3 yields 11 . Analysis of the global reactivity indices as well as the thermodynamic data for this domino process indicate that while the large electrophilic character of 1 together with the large nucleophilic character of 2 are responsible for the participation of these reagents in a polar Diels–Alder react…

DieneCondensed Matter PhysicsPhotochemistryBiochemistrychemistry.chemical_compoundElimination reactionNucleophilechemistryCascade reactionComputational chemistryReagentElectrophileReactivity (chemistry)Physical and Theoretical ChemistryDerivative (chemistry)Journal of Molecular Structure: THEOCHEM
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Selective, homogeneous hydrogenation of cycloheptatriene to cycloheptene catalyzed by (η4-cycloocta-1,5-diene)(η6-cyclohepta-1,3,5-triene)ruthenium(0)

1980

Abstract In the presence of small amounts of [Ru(η 4 -COD)](η 6 -C 8 H 10 )] (1), cycloheptatriene is hydrogenated to cycloheptene, under one atmosphere of hydrogen at room temperature in homogeneous phase. The formation of a small amount of cyclooctene and the existence of an induction period, which do not occur when [Ru(η 4 -COD)(η 6 -C 7 H 8 )] (2) is used as the catalyst, suggest that 2 is the real catalyst. The selectivity of this hydrogenation is 100% in n-hexane as solvent, 99.5% in THF, and low in ethanol. Conversion is quantitative in THF and ethanol, but not more than 65% in n-hexane. In the presence of 1 or 2, cycloheptene is rapidly hydrogenated to cycloheptane in THF and ethano…

DieneInduction periodOrganic Chemistrychemistry.chemical_elementCycloheptatrienePhotochemistryBiochemistryMedicinal chemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryCycloocteneMaterials ChemistryCycloheptenePhysical and Theoretical ChemistryCycloheptaneJournal of Organometallic Chemistry
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Selective homogeneous hydrogenation of cycloocta-1,5, and cycloocta-1,3-diene to cyclooctene in the presence of (η4-cycloocta-1,5-diene)(η6-cycloocta…

1983

Cyclooctadiene isomers (1,3- and 1,5-COD) are selectively, homogenously hydrogenated to cyclooctene (C8H14) in tetrahydrofuran (THF) solution, under mild conditions of temperature (20 °C) and hydrogen pressure (1 atm), in the presence of catalytic amounts of (cycloocta-1,5-diene)(cycloocta-1,3,5,-triene)ruthenium(0), [Ru(η4-COD)(η6-C8H10)] (1). The rate of hydrogenation is higher when 1,3-COD is the substrate. Evidence for the isomerization 1,5-COD → 1,3-COD is reported. Similar studies carried out in several alcoholic solutions, although showing a decreased selectivity in the hydrogenation, confirm the isomerization 1,5-COD → 1,3-COD, and allow a discrimination between the isomerization an…

DieneNorbornadienechemistry.chemical_elementNoyori asymmetric hydrogenationPhotochemistryMedicinal chemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryCycloocteneMaterials ChemistryPhysical and Theoretical ChemistryIsomerizationCyclooctadieneInorganica Chimica Acta
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Reactions of Alkenes and Alkynes with an Acyclic Silylene and Heavier Tetrylenes under Ambient Conditions

2014

Cycloaddition reactions of the acyclic silylene Si(SAriPr4)2 (AriPr4 = C6H3-2,6(C6H3-2,6-iPr2)2) with a variety of alkenes and alkynes were investigated. Its reactions with the alkynes phenylacetylene and diphenylacetylene and the diene 2,3-dimethyl-1,3-butadiene yielded silacycles (AriPr4S)2tiebar above startSi(CH═tiebar above endCPh) (1), (AriPr4S)2tiebar above startSi(PhC═tiebar above endCPh) (2), and (AriPr4S)2tiebar above startSiCH2CMeCMetiebar above endCH2 (3) at ambient temperature. The compounds were characterized by X-ray crystallography, 1H, 13C, and 29Si NMR spectroscopy, and IR spectroscopy. No reaction was observed with more substituted alkenes such as propene, (Z)-2-butene, te…

DieneTrimethylsilylacyclic silyleneAlkynealkeenit ja alkyynitPhotochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundraskaammat tetryleenitalkenes and alkynesCyclopenteneambient conditionssykloadditioreaktiotPhysical and Theoretical Chemistryasyklinen silyleeniDiphenylacetyleneta116chemistry.chemical_classificationOrganic ChemistrySilylenecyloaddition reactionsCycloadditionPhenylacetylenechemistrynormaalit ympäristön olosuhteethevier tetrylenes
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