Search results for "thiophene"

showing 10 items of 284 documents

Benzothiazolethione complexes of coinage metals: from mononuclear complexes to clusters and polymers

2019

Abstract The reactions of 2(3H)-benzothiazolethione (Hbtt) with [AuCl(tetrahydrothiophene)] and CuBr2 were studied, and found to yield a tetranuclear cluster compound [Au(btt)]4 [1] and a polymeric structure [CuBr(btt-btt)]n.nTHF (2). Crystallographic and spectroscopic methods were used for the characterization. In 1, the monoanionic ligand acted as a bidentate bridging N,S-donor giving a molecular cluster structure of an asymmetric coordination isomer. In the formation of 2, the ligand was dimerized by forming a S–S bond after deprotonation, and coordination via nitrogen donors to metal atoms took place leading to a polymeric structure. To clarify the diversity of reactions of Hbtt with co…

DenticityCoinage metalschemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesCopper0104 chemical sciencesMetalCoordination isomerismCrystallographychemistry.chemical_compoundDeprotonationchemistryvisual_artvisual_art.visual_art_mediumCluster (physics)General Materials Science0210 nano-technologyTetrahydrothiopheneSolid State Sciences
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Direct arylation of heterocycles: the performances of ferrocene-based polyphosphane ligands in palladium-catalyzed C-H bond activation

2010

International audience; The palladium-catalyzed direct arylation of alkylated- furan, thiophene, and thiazole and benzoxazole heterocycles with electronically and sterically deactivated bromoarenes was selectively and efficiently promoted by ferrocenyl polyphosphanes. In this C[BOND]H bond activation reaction of heteroaromatics, the performances of polydentate di-, tri-, and tetraphosphane ligands were compared, showing that the triphosphane 1,1′,2-tris(diphenylphosphino)-4-tert-butylferrocene 3 was the most effective for the coupling. The introduction of more electron-donating (iPr) or electron-withdrawing (furyl) groups on the phosphorus atoms did not improve the ligand performances. The …

Denticitychemistry.chemical_elementCH activation010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisThiopheneOrganic chemistryChelation[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryThiazoleheterocycles010405 organic chemistryLigandOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.CATA]Chemical Sciences/CatalysisBenzoxazolepalladiumhomogeneous catalysis0104 chemical sciencesTriphosphanechemistryligands effectsPalladium
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The pyrrole moiety as a template for COX-1/COX-2 inhibitors

2000

Aroyl- and thiophene-substituted pyrrole derivatives have been synthesized as a new class of COX-1/COX-2 inhibitors. The inhibition of COX-1 was evaluated in a biological system using bovine PMNLs as the enzyme source, whereas LPS-stimulated human monocytes served as the enzyme source for inducible COX-2. The determination of the concentration of arachidonic acid metabolites was performed by HPLC for COX-1 and RIA for COX-2. Variation of the substitution pattern led to a series of active compounds which showed inhibition for COX-1 and COX-2. Structural requirements for the development of COX-1/COX-2 inhibitors are discussed.

DiclofenacNeutrophilsStereochemistryIndomethacinThiophenesHigh-performance liquid chromatographyMonocytesPyrrole derivativeschemistry.chemical_compoundDrug DiscoveryAnimalsHumansStructure–activity relationshipMoietyCyclooxygenase InhibitorsPyrrolesSulfonesPyrrolePharmacologychemistry.chemical_classificationArachidonic AcidCyclooxygenase 2 InhibitorsMolecular StructureAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryMembrane ProteinsGeneral MedicineIsoenzymesEnzymechemistryMembrane proteinBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesCyclooxygenase 1Leukocytes MononuclearCattleArachidonic acidEuropean Journal of Medicinal Chemistry
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Polar Diels–Alder reactions using electrophilic nitrobenzothiophenes. A combined experimental and DFT study

2015

Abstract The reactions between 2- and 3-nitrobenzothiophenes with three dienes of different nucleophilicity, 1-methoxy-3-trimethylsilyloxy-1,3-butadiene, 1-trimethylsilyloxy-1,3-butadiene and isoprene developed in anhydrous benzene and alternative under microwave irradiation with molecular solvents or in free solvent conditions, respectively, for produce dibenzothiophenes permit to conclude that both nitroheterocycles act as electrophile with the cited dienes. In the cases of the dienes 1-methoxy-3-trimethylsilyloxy-1,3-butadiene and 1-trimethylsilyloxy-1,3-butadiene which posses major nucleophilicity the observed product is the normal cycloaddition one. However when the diene is isoprene t…

DieneOrganic ChemistryCycloadditionAnalytical ChemistryInorganic ChemistrySolventchemistry.chemical_compoundchemistryNucleophileDibenzothiopheneElectrophileOrganic chemistryBenzeneSpectroscopyIsopreneJournal of Molecular Structure
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Duloxetine serum concentrations and clinical effects. Data from a therapeutic drug monitoring (TDM) survey.

2009

INTRODUCTION The aim of this study was to relate drug concentrations in serum and clinical effects in patients treated with the new antidepressant duloxetine. METHODS Data were obtained from a newly established therapeutic drug monitoring (TDM) survey. Duloxetine was measured using HPLC with UV detection and clinical effects by the clinical global impressions (CGI) scale for improvement. RESULTS The study included 103 depressed inpatients (69% female). Patients under duloxetine monotherapy who were very much improved according to CGI had significantly (p<0.05) higher serum levels than patients with moderate, minimal or lacking improvement (mean+/-SD and range, 93+/-53 ng/mL and 30-182 ng/mL…

DrugAdultMalemedicine.medical_specialtyUltraviolet Raysmedia_common.quotation_subjectUrologyThiophenesPharmacologyDuloxetine HydrochlorideDuloxetine HydrochlorideSeverity of Illness Indexchemistry.chemical_compoundYoung AdultSeverity of illnessMedicineDuloxetineHumansPharmacology (medical)Chromatography High Pressure Liquidmedia_commonAgedAged 80 and overDepressive DisorderReceiver operating characteristicmedicine.diagnostic_testDose-Response Relationship Drugbusiness.industrySpectrum AnalysisGeneral MedicineSerum concentrationMiddle AgedAntidepressive AgentsPsychiatry and Mental healthDose–response relationshipTreatment OutcomechemistryROC CurveTherapeutic drug monitoringFemaleDrug MonitoringbusinessPharmacopsychiatry
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Electrochemical Fabrication of High K Niobium-Tantalum Mixed Oxides/Poly 3-4 Ethylene Dioxythiophene Junctions.

2012

Electrochemical Fabrication High K Niobium-Tantalum Mixed Oxides Poly 3-4 Ethylene DioxythiopheneSettore ING-IND/23 - Chimica Fisica Applicata
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From monolayer to multilayer N-channel polymeric field-effect transistors with precise conformational order

2012

Monolayer field-effect transistors based on a high-mobility n-type polymer are demonstrated. The accurate control of the long-range order by Langmuir-Schafer (LS) deposition yields dense polymer packing exhibiting good injection properties, relevant current on/off ratio and carrier mobility in a staggered configuration. Layer-by-layer LS film transistors of increasing thickness are fabricated and their performance compared to those of spin-coated films.

Electron mobilityMaterials scienceTransistors ElectronicPolymersNanotechnologyThiophenesNaphthalenesTransistorslaw.inventionlawMonolayerElectronicDeposition (phase transition)General Materials Sciencemonolayer field-effect transistorchemistry.chemical_classificationbusiness.industrysemiconducting polymersMechanical EngineeringTransistorTransistor monolayer polymers orderPolymercharge transportchemistrylayered materialsMechanics of MaterialsN channelOptoelectronicsField-effect transistorbusiness
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Flexible diphenylsulfone versus rigid dibenzothiophene-dioxide as acceptor moieties in donor-acceptor-donor TADF emitters for highly efficient OLEDs

2020

DG acknowledges funding from the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177 . This research is/was funded by the European Regional Development Fund according to the supported activity ‘ Research Projects Implemented by World-class Researcher Groups ’ under Measure No. 01.2.2-LMT-K-718 . Ministry of Science and Technology (MOST), Taiwan , Grant No. MOST 106-2923-E-155-002-MY3 . This work was also supported by the Ministry of Education and Science of Ukraine (projects no. 0117U003908 and 0118U003862 ), and by the Olle Engkvist Byggmästare foundation (contract No. 189-0223 ). The quantum-chemical calculations were performed with computational resources provided by the High Performance Comp…

Electron mobilityPhotoluminescenceMaterials science02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesBiomaterialsMaterials ChemistryOLED:NATURAL SCIENCES:Physics [Research Subject Categories]MoleculeMoietySinglet stateDibenzothiophene dioxideElectrical and Electronic Engineeringdi-tert-butyldimethyldihydroacridineGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsDiphenylsulfoneAcceptor0104 chemical sciencesElectronic Optical and Magnetic MaterialsThermally activated delayed fluorescencQuantum efficiency0210 nano-technologyBipolar charge transportOrganic Electronics
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Poly(naphthalenediimidequaterthiophene):Poly(hexyilthiophene) Heterojunctions. Efficient Polymer-to-Polymer Electron Transfer Interfaces

2013

Organic thin films solar cells and plastic solar cells [1] have attracted the attention of the scientific community especially as regards the performance of new conjugated polymers including their interfaces [2-4]. In this work, poly(naphthalenediimidequaterthiophene) (PNDIT4) and poly(hexyilthiophene) (P3HT) have been employed, for the first time, for engineering planar and bulk heterojunctions by the synergetic use of two techniques: electropolymerization and layer by layer deposition. Electropolymerization has been used for obtaining PNDIT4 thin films on transparent ITO/PET electrodes, starting from the synthesized monomer. Inverse Langmuir-Schaefer technique has been employed for deposi…

Electron transfer poly(naphthalenediimidequaterthiophene)Settore CHIM/02 - Chimica Fisica
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Chlorinated dioxins and dibenzothiophenes in fly ash samples from combustion of peat, wood chips, refuse derived fuels and liquid packaging boards

1995

Abstract Peat, wood chips, refuse derived fuel and liquid packaging board in different combinations were burned at a temperature of at least 850 °C. Fly ash samples from these combustions were analyzed for polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzothiophenes (PCDBTs) by high resolution GC/MS. The concentrations of tri- and tetrachlorodibenzothiophenes and tri-, tetra- and pentachlorodioxins were highest when mixtures of wood chips and refuse derived fuel (RDF) were burned. The fly ash from the combustion of pure peat pellets did not contain any polychlorinated dibenzothiophenes. When wood chips and RDF were burned the concentrations of chlorinated compounds in fly…

Environmental EngineeringPeatrefuseanalysisHealth Toxicology and MutagenesisPelletschemistry.chemical_elementHigh resolutionCombustionLiquid packaging boarddioxinsChlorineEnvironmental ChemistryRefuse-derived fuelwood fuelsWaste managementPublic Health Environmental and Occupational HealthemissionsGeneral MedicineGeneral Chemistrychlorine aromatic compoundsPollutionwood shipsfly ashchemistrythiophenesFly ashpeatcombustion
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