Search results for "thiophene"

showing 10 items of 284 documents

Liquid chromatographic determination of planar aromatic sulphur compounds in crude oil

1989

Oxydation des dibenzothiophenes en sulfones et analyse par chromatographie liquide haute performance

ChromatographyChemistryOrganic Chemistrychemistry.chemical_elementGeneral MedicineCrude oilBiochemistrySulfurThin-layer chromatographyAnalytical ChemistrySulfonechemistry.chemical_compoundDibenzothiopheneOrganic chemistryJournal of Chromatography A
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New benzothieno[3,2-d]-1,2,3-triazines with antiproliferative activity: synthesis, spectroscopic studies, and biological activity.

2014

New benzothieno[3,2-d]-1,2,3-triazines, together with precursors triazenylbenzo[b]thiophenes, were designed, synthesized and screened as anticancer agents. The structural features of these compounds prompted us to investigate their DNA binding capability through UV–vis absorption titrations, circular dichroism, and viscometry, pointing out the occurrence of groove-binding. The derivative 3-(4-methoxy-phenyl)benzothieno[3,2-d]-1,2,3-triazin-4(3H)-one showed the highest antiproliferative effect against HeLa cells and was also tested in cell cycle perturbation experiments. The obtained results assessed for the first time the anticancer activity of benzothieno[3,2-d]-1,2,3-triazine nucleus, and…

Circular dichroismStereochemistryClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsThiophenesBiochemistryHeLachemistry.chemical_compoundStructure-Activity RelationshipSettore BIO/10 - BiochimicaDrug DiscoveryStructure–activity relationshipMoleculeHumansMolecular BiologyCell ProliferationbiologyDose-Response Relationship DrugMolecular StructureChemistryCell growthTriazinesViscosityCircular DichroismOrganic ChemistryCell CycleBiological activityCell cyclebiology.organism_classificationSettore CHIM/08 - Chimica FarmaceuticaCombinatorial chemistrySettore CHIM/03 - Chimica Generale E InorganicaMolecular MedicineBenzothienotriazines Antiproliferative activity Spectroscopic studies Cell-cycle analysis VLAKSpectrophotometry UltravioletDrug Screening Assays AntitumorDNAHeLa CellsBioorganicmedicinal chemistry letters
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The fragmentation of 5- and 3-substituted thiophene-2-carboxamides under electron impact

1980

The 70 eV electron impact mass spectra of twelve 5- and 3-substituted thiophene-2-carboxamides are discussed with the aid of exact mass measurements and labelling experiments. All mass spectra exhibit pronounced molecular ions. Some isomeric 5- and 3-substituted title compounds can be differentiated by mass spectrometry. The fragmentation is influenced by a strong ‘ortho-effect’ which activates the NH3 elimination. In the other cases the most important fragmentation is NH2˙ loss, followed by CO elimination.

Collision-induced dissociationAnalytical chemistryPhotochemistryMass spectrometryBiochemistryIonMasschemistry.chemical_compoundchemistryFragmentation (mass spectrometry)Mass spectrumThiopheneMolecular MedicineInstrumentationSpectroscopyElectron ionizationOrganic Mass Spectrometry
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Tuning of the photoinduced charge transfer process in donor-acceptor "double cable" copolymers

2003

The covalent linking of acceptor molecules to electron donating conjugated polymer is an approach for the development of new photoactive materials for the fabrication of organic photoelectric conversion devices. With this strategy we have designed a polyalkylthiophene copolymer series containing in the side chain anthraquinone molecules as electron acceptor. The peculiar features of the copolymers are the good processability and the ease in tailoring the content of acceptor moieties. Their potential use as photoactive materials is investigated in terms of the photoinduced charge transfer properties, studied by FTIR photoinduced absorption and Light Induced Electron Spin Resonance spectrosco…

Condensed Matter PhysicConjugated systemPhotochemistryAnthraquinonePhotoinduced electron transferlaw.inventionchemistry.chemical_compoundlawMaterials ChemistryMoleculeDonor-acceptor alkylthiophene copolymerPhotoinduced charge transferElectron paramagnetic resonanceMechanical EngineeringElectronic Optical and Magnetic MaterialMetals and AlloysSettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsAcceptorElectronic Optical and Magnetic MaterialschemistryMechanics of MaterialsCovalent bondPolythiopheneLight-induced electron spin resonancePhotoinduced absorption
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Current density maps, magnetizability, and nuclear magnetic shielding tensors of bis-heteropentalenes. III. Thieno-thiophene isomers

2005

Near Hartree–Fock values of the magnetic susceptibility and nuclear magnetic shielding of bis-heteropentalenes consisting of two thiophene units ([2,3-b], [3,2-b], [3,4-b], and [3,4-c] isomers) have been estimated via computational schemes relying on continuous transformation of the origin of the current density within the coupled Hartree–Fock approximation and extended gaugeless Gaussian basis sets. The results are compared with those obtained via London gauge-including orbitals. Maps of streamlines and the modulus of the ring current density induced by a magnetic field normal to the molecular plane are reported for the three isomers of higher symmetry, showing that the intense diamagnetic…

Condensed matter physicsChemistryBiophysicsElectronCondensed Matter PhysicsMolecular physicsMagnetic susceptibilityCurrent density maps; magnetizability; nuclear magnetic shielding tensors; thieno-thiophene isomersMagnetic fieldchemistry.chemical_compoundMagnetic anisotropyElectromagnetic shieldingThiopheneDiamagnetismTensorPhysical and Theoretical ChemistryMolecular Biology
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Light induced electropolymerization of poly(3,4-ethylenedioxythiophene) on niobium oxide

2010

Abstract The photoelectrochemical polymerization of poly(3,4-ethylenedioxythiophene), PEDOT, was successfully realized on anodic film grown to 50 V on magnetron sputtered niobium. Photocurrent Spectroscopy was employed to study the optical properties of Nb/Nb 2 O 5 /PEDOT/electrolyte interface in a large range of potential, and to get an estimate of the band gap and flat band potential of both the oxide and the polymer. Scanning Electron Microscopy was used to study the morphology of PEDOT. Both the optical and morphological features of the photoelectrochemically grown polymer were compared with those showed by PEDOT electropolymerized on gold conducting substrate.

Conductive polymerPhotocurrentMaterials scienceBand gapGeneral Chemical EngineeringPhotoelectrochemistryInorganic chemistryOxidephoto-electropolymerization poly(34-ethylenedioxythiophene) niobium oxidechemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicatachemistryPEDOT:PSSChemical engineeringBand gap Niobium oxide PEDOT PhotoelectrochemistryElectrochemistryNiobium oxidePoly(34-ethylenedioxythiophene)Electrochimica Acta
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Ester-functionalized poly(3-alkylthiophene) copolymers : synthesis, physicochemical characterization and performance in bulk heterojunction organic s…

2013

Abstract The introduction of functional moieties in the donor polymer (side chains) offers a potential pathway toward selective modification of the nanomorphology of conjugated polymer:fullerene active layer blends applied in bulk heterojunction organic photovoltaics, pursuing morphology control and solar cell stability. For this purpose, two types of poly(3-alkylthiophene) random copolymers, incorporating different amounts (10/30/50%) of ester-functionalized side chains, were efficiently synthesized using the Rieke method. The solar cell performance of the functionalized copolymers was evaluated and compared to the pristine P3HT:PCBM system. It was observed that the physicochemical and opt…

Conductive polymerchemistry.chemical_classificationMaterials scienceOrganic solar cellfullerenesGeneral ChemistryPolymerCondensed Matter PhysicsPolymer solar cellbulk heterojunction solar cellsElectronic Optical and Magnetic Materialslaw.inventionBiomaterialschemistry.chemical_compoundchemistrylawSolar cellPolymer chemistryMaterials ChemistryCopolymerSide chainPolythiopheneorganic photovoltaicsElectrical and Electronic Engineeringconductive polymers
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Polymer-based symmetric electrochromic devices

1999

Abstract The fact that conjugated polymers repeatedly undergo electrochemical doping/undoping processes, which are accompained by color changes, makes these materials very attractive, and much effort has been devoted to their use in advanced devices. There is renewed interest in electroactive polymers that reversibly undergo both p- and n-doping because of their potential application in symmetric electrochemical devices. We employed fused molecules, dithienothiophenes, as monomers to obtain polymers with a narrow band gap suitable for n- and p-doping. The performance results of two symmetric electrochromic devices having as electrodes both poly(dithieno[3,4-b:3',4'-d]thiophene) (pDTT1) and …

Conductive polymerchemistry.chemical_classificationMaterials scienceRenewable Energy Sustainability and the EnvironmentDopingNanotechnologyPolymerConjugated systemElectrochromic devicesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMonomerchemistryThiopheneElectroactive polymersOrganic chemistrySolar Energy Materials and Solar Cells
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Soil remediation: humic acids as natural surfactants in the washings of highly contaminated soils

2005

The remediation of the highly contaminated site around the former chemical plant of ACNA (near Savona) in Northern Italy is a top priority in Italy. The aim of the present work was to contribute in finding innovative and environmental-friendly technology to remediate soils from the ACNA contaminated site. Two soils sampled from the ACNA site (A and B), differing in texture and amount and type of organic contaminants, were subjected to soil washings by comparing the removal efficiency of water, two synthetic surfactants, sodium dodecylsulphate (SDS) and Triton X-100 (TX100), and a solution of a natural surfactant, a humic acid (HA) at its critical micelle concentration (CMC). The extraction …

Conservation of Natural ResourcesOctoxynolSoil textureEnvironmental remediationHealth Toxicology and MutagenesisSettore AGR/13 - Chimica AgrariaThiophenesToxicologyHydrocarbons Aromaticcomplex mixturesSoilSonicationSurface-Active AgentsSoil PollutantsHumic acidHumic Substanceschemistry.chemical_classificationSoil-remediation Soil-washing Soxhlet Sonication Contaminated soilsExtraction (chemistry)Sodium Dodecyl SulfateWaterGeneral MedicineContaminationPollutionSoil contaminationItalychemistryChemical IndustryCritical micelle concentrationEnvironmental chemistrySoil waterEnvironmental Pollution
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Role of photoactive layer morphology in high fill factor all-polymer bulk heterojunction solar cells

2011

We report on the realization of all-polymer solar cells based on blends of poly(3-hexylthiophene-2,5-diyl) (P3HT) as a donor and poly{[N,N'-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5'-(2,2'-bithiophene)} (P(NDI2OD-T2)) as an acceptor. High fill factors are demonstrated for the first time in this class of devices suggesting high dissociation efficiency for the bounded electron-hole pairs and balanced electron and hole mobility along the thin films. The use of the high-mobility n-type P(NDI2OD-T2) polymer enables us to overcome one of the problems limiting the efficiency of all-polymer solar cells, resulting in fill factors comparable with those reported for …

DYNAMICSElectron mobilityMaterials scienceFullerenePHOTOVOLTAIC DEVICESLIGHT-INTENSITY DEPENDENCEBLENDSPolymer solar cellPhotoactive layerMaterials ChemistryThin filmSettore CHIM/02 - Chimica FisicaOpen-circuit voltagebusiness.industryORIGINPOLY(3-HEXYLTHIOPHENE)General ChemistryHybrid solar cellAcceptorTRANSPORTOPEN-CIRCUIT VOLTAGEsolar cells bulk heterojunctions devices organic electronicsTRANSISTORSOptoelectronicsbusinessCONJUGATED POLYMERS
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