Search results for "thiophene"

showing 10 items of 284 documents

Polydithienothiophenes: Two new conjugated materials with narrow band gap

1997

Abstract The electrochemical polymerisation of dithieno[3,4-b:3',2'-d]thiophene and dithieno[3,4-b:2',3'-d]thiophene leads to conjugated materials with narrow band gap in which the p- and n-doping processes are possible in organic electrolytes. The spectroelectrochemical study of these polymers is reported.

chemistry.chemical_classificationMaterials scienceMechanical EngineeringMetals and AlloysElectrolytePolymerConjugated systemCondensed Matter PhysicsElectrochemistryPhotochemistryElectronic Optical and Magnetic MaterialsNarrow bandchemistry.chemical_compoundchemistryPolymerizationMechanics of MaterialsPolymer chemistryMaterials ChemistryThiopheneElectrical conductor
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Optimization of Polymer Blue-Light-Emitting Devices by Introducing a Hole-Injection Layer Doped with the Molecular Nanomagnet [Mn12O12(H2O)4(C6F5COO)…

2006

chemistry.chemical_classificationMaterials scienceMolecular magnetsbusiness.industryMechanical EngineeringDopingHole injection layerPolymerNanomagnetElectron transport chainchemistry.chemical_compoundchemistryMechanics of MaterialsOptoelectronicsGeneral Materials SciencebusinessPoly(34-ethylenedioxythiophene)Blue lightAdvanced Materials
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High‐Efficiency Perovskite Solar Cells Using Molecularly Engineered, Thiophene‐Rich, Hole‐Transporting Materials: Influence of Alkyl Chain Length on …

2016

The synthesis and characterization of a series of novel small-molecule hole-transporting materials (HTMs) based on an anthra[1,2-b:4,3-b′:5,6-b′′:8,7-b′′′]tetrathiophene (ATT) core are reported. The new compounds follow an easy synthetic route and have no need of expensive purification steps. The novel HTMs are tested in perovskite solar cells and power conversion efficiencies (PCE) of up to 18.1% under 1 sun irradiation are measured. This value is comparable with the 17.8% efficiency obtained using 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene as a reference compound. Similarly, a significant quenching of the photoluminescence in the first nanosecond is observed, ind…

chemistry.chemical_classificationPhotoluminescenceQuenching (fluorescence)Materials scienceRenewable Energy Sustainability and the EnvironmentEnergy conversion efficiency02 engineering and technologyConductivity010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences7. Clean energy0104 chemical scienceschemistry.chemical_compoundChemical engineeringchemistryThiopheneOrganic chemistryGeneral Materials ScienceSolubility0210 nano-technologyAlkylPerovskite (structure)Advanced Energy Materials
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Asymmetric Synthesis of Spiro Tetrahydrothiophene-indan-1,3-diones via a Squaramide-Catalyzed Sulfa-Michael/Aldol Domino Reaction

2016

Synthesis 48(08), 1131-1138(2016). doi:10.1055/s-0035-1560412

chemistry.chemical_classificationSpiro compound010405 organic chemistryOrganic ChemistrySquaramideEnantioselective synthesis540010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisDomino0104 chemical scienceschemistry.chemical_compoundchemistryCascade reactionAldol reactionOrganocatalysisddc:540Organic chemistryTetrahydrothiophene
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ChemInform Abstract: Conjugated Compounds Based on Vinylthiazole Units.

2008

Conjugated oligomers attract increasing attention because of their interesting properties in materials science [1]. Moreover, they are model compounds for conjugated polymers. Molecules polarized by electronic effects, in particular push-pull systems having terminal donor-acceptor substitution represent a special class of such oligomers [2]. Their major applications are in the field of nonlinear optics (NLO), twophoton absorption (TPA), two-photon induced fluorescence (TPIF), and photorefractive materials (PR). Fig. 1 illustrates known 2,5-thienylenevinylenes with zwitterionic resonance structures 1 (D = NR2; A = NO2, CHO, SO2R; n = 1, 2) [3, 4]. The corresponding compounds 2 with thiazole …

chemistry.chemical_classificationStereochemistryElectron donorGeneral MedicineConjugated systemElectron acceptorRing (chemistry)Medicinal chemistrychemistry.chemical_compoundchemistryThiopheneElectronic effectMoleculeThiazoleChemInform
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ChemInform Abstract: New Acetylenes from Chrysanthemum coronarium L.

1990

The investigation of the aerial parts of Chrysanthemum coronarium yielded, in addition to several known compounds, two new acetylenic sulfoxides 9 and 10, and a new thiophene spiroacetal enol ether 11. Their structures were deduced by spectroscopic and chemical methods.

chemistry.chemical_classificationchemistry.chemical_compoundChemistryChrysanthemum coronariumThiopheneEnol etherOrganic chemistryGeneral MedicineChemInform
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Conjugated Compounds Based on Vinylthiazole Units

2007

Conjugated oligomers attract increasing attention because of their interesting properties in materials science [1]. Moreover, they are model compounds for conjugated polymers. Molecules polarized by electronic effects, in particular push-pull systems having terminal donor-acceptor substitution represent a special class of such oligomers [2]. Their major applications are in the field of nonlinear optics (NLO), twophoton absorption (TPA), two-photon induced fluorescence (TPIF), and photorefractive materials (PR). Fig. 1 illustrates known 2,5-thienylenevinylenes with zwitterionic resonance structures 1 (D = NR2; A = NO2, CHO, SO2R; n = 1, 2) [3, 4]. The corresponding compounds 2 with thiazole …

chemistry.chemical_classificationchemistry.chemical_compoundchemistryThiopheneElectronic effectMoleculeElectron donorGeneral ChemistryConjugated systemElectron acceptorRing (chemistry)ThiazoleMedicinal chemistryZeitschrift für Naturforschung B
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Multicomponent Synthesis of Benzothiophen-2-acetic Esters by a Palladium Iodide Catalyzed S-cyclization – Alkoxycarbonylation Sequence

2021

A catalytic carbonylative approach to the multicomponent synthesis of benzothiophene derivatives from simple building blocks [1-(2-(methylthio)phenyl)prop-2-yn-1-ols, carbon monoxide, and an alcohol)] is presented. It is based on an S-cyclization-demethylation-alkoxycarbonylation-reduction sequence promoted by the PdI2/KI catalytic system, occurring under relatively mild conditions (40 atm, 80 °C, 15 h). Benzothiophene-2-acetic esters are obtained in moderate to good yields (35–70%) starting from variously substituted substrates in combination with different alcohols as external nucleophiles (17 examples). (Figure presented.).

chemistry.chemical_classificationmulticomponent reactionIodidechemistry.chemical_elementGeneral ChemistrycarbonylationSettore CHIM/06 - Chimica OrganicapalladiumCombinatorial chemistryCatalysischemistrybenzothiophenesS-cyclizationCarbonylationPalladiumSequence (medicine)
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Efficient palladium catalyzed synthesis of heteroaromatic sulfoxides

2007

Abstract The present Letter describes the efficient synthesis of novel heteroaromatic sulfoxides by means of a palladium catalyzed heteroarylation of sulfenate anions. Triazolopyridine, pyridine and thiophene sulfoxides can be obtained under mild conditions and in high yield from the corresponding heteroaryl bromides.

chemistry.chemical_compoundChemistryYield (chemistry)Organic ChemistryDrug DiscoveryPyridineThiophenechemistry.chemical_elementTriazolopyridineBiochemistryCombinatorial chemistryCatalysisPalladiumTetrahedron Letters
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Linear free energyortho-correlations in the thiophene series. Part IX . Kinetics of esterification with diazodiphenylmethane of some 3-, 4-, and 5-su…

1981

The rate constants for the esterification of some 3-, 4-, and 5-substituted thiophene-2-carboxylic acids with diazodiphenylmethane in methanol at 25° have been measured. The reactivity of some para- and ortho-substituted benzoic acids has also been determined. Logarithmic kinetic constants for ortho-, meta-, and para-like substituted thiophene-2-carboxylic acids furnish an excellent linear free energy relationship when plotted versus Δpka (β 0.89, r 0.989, C.L. > 99.9%, n 18, i 0.04), thus confirming the peculiar behaviour of five-membered ring derivatives. The correlation with σH values offers an additional proof of the hyper-ortho character of the 2,3-relation in thiophene derivatives. pa…

chemistry.chemical_compoundDiazodiphenylmethaneReaction rate constantChemistryOrganic ChemistryKineticsThiopheneOrganic chemistryReactivity (chemistry)MethanolFree-energy relationshipRing (chemistry)Medicinal chemistryJournal of Heterocyclic Chemistry
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