Search results for "POLYTHIOPHENES"

showing 6 items of 6 documents

Recognition of oxovanadium(V) species and its separation from other metal species through selective complexation by some acyclic ligands

1998

Acyclic molecules possessing –OH (phenoxo and alkoxo type) groups and imine or amine moieties have been developed to sense the specific preference for VO3+ species. These molecules also showed a capability to quantitatively separate oxovanadium(V) species from a reaction mixture containing metal species of V, Mo, U, Fe, and Mn ions in solution. A cascade quantitative separation of VO3+ followed by cis–MoO2+2 followed by trans –UO2+2 species is demonstrated from their mixture. Synthesis and structural details of oxo-species of vanadium molybdenum and uranium are also discussed. Factors influencing the complexation of these molecules towards oxo metal species of V, Mo and U are also addressed.

Absorption SpectraPolyanilineStereochemistryMetal ions in aqueous solutionImineCis-Dioxome(Vi)Vanadiumchemistry.chemical_elementTrans-Dioxoo(Iv)Medicinal chemistryInorganic ChemistryMetalSynthesisTransmetalationchemistry.chemical_compoundOxidationElectronicMaterials ChemistryPolythiophenesMoleculeSelective ComplexationPhysical and Theoretical ChemistryConducting PolymerCis-Dioxov(V)TransmetallationChemistryReactivityChemistryRecognitionMolybdenumvisual_artvisual_art.visual_art_mediumAmine gas treatingCrystallographicPolyhedron
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Poly(alkoxyphenylene-thienylene) Langmuir-Schäfer thin-films for advanced performance transistors

2005

Solution processed Langmuir-Scha ̈fer and cast thin films of regioregular poly(2,5-dioctyloxy-1,4- phenylene-alt-2,5-thienylene) are investigated as transistor active layers. The study of their field-effect properties evidences that no transistor behavior can be seen with a cast film channel material. This was not surprising considering the twisted conformation of the polymer backbone predicted by various theoretical studies. Strikingly, the Langmuir-Scha ̈fer (LS) thin films exhibit a field-effect mobility of 5 × 10-4 cm2/V‚s, the highest attained so far with an alkoxy-substituted conjugated polymer. Extensive optical, morphological, and structural thin-film characterization supports the a…

LangmuirMaterials sciencePHENYLENEGeneral Chemical EngineeringNanotechnologylaw.inventionlawPhenyleneSTILLE COUPLING REACTIONMaterials ChemistryThin filmConductive polymerbusiness.industryREGIOREGULAR POLY(3-HEXYLTHIOPHENE)TransistorGeneral ChemistryOPTICAL-PROPERTIESSolution processedBLODGETT-FILMSCONDUCTING POLYMERSOptoelectronicsField-effect transistorPOLYTHIOPHENESFIELD-EFFECT TRANSISTORSREPEAT UNITSbusinessCONJUGATED POLYMERS
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Investigation of NLO Properties of some Selected Polythiophenes Electrodeposited on ITO Glasses

2008

NLO Properties Polythiophenes
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Enhanced power-conversion efficiency in organic solar cells incorporating polymeric compatibilizers

2018

Organic solar cells Polythiophenes Charge transfer
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NLO properties of polythiophenes galvanostatically electrodeposited on ITO glasses

2008

International audience; A study of nonlinear optical properties of ClO4-doped polythiophenes, galvanostatically electrodeposited on ITO glasses, was carried out using second and third harmonic generation measurements. The effect of the oxidation state of the polymeric films was studied by comparing the nonlinear optical response of oxidised and reduced polythiophenes. Reduced polymeric films show higher values of the second and third order susceptibilities and a lower absorbance in respect to the oxidised ones. The morphology of the polythiophene films was studied by scanning electron and atomic force microscopes.

[SDV] Life Sciences [q-bio][SDV]Life Sciences [q-bio]PolythiophenesNLO propertiesPolythiophene SHG THG NLO propertiesSHGTHG
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Donor-Acceptor Polythiophene Copolymers with Tunable Acceptor content for Photoelectric Conversion Devices

2004

The synthesis and characterization of a new series of substituted polythiophenes containing an electron acceptor anthraquinone moiety in the side chain are reported. The acceptor molar content was varied by the co-polymerization of both alkylthiophene and thiophene bearing anthraquinone monomers in different ratios. NMR analysis shows a good correlation between the monomer feed composition at the beginning of the polymerization and the actual unit composition of the backbone. The conjugation length and the chemical composition of the copolymers as a function of the molecular weight have been studied by size exclusion chromatography. Small angle X-ray scattering and UV-Vis absorption spectra…

chemistry.chemical_classificationChemistryElectron donorSettore CHIM/06 - Chimica OrganicaGeneral ChemistryConjugated polymersElectron acceptorPhotochemistryAcceptorAnthraquinoneDonor-acceptorchemistry.chemical_compoundPolymerizationTetracyanoanthraquinodimethaneMaterials ChemistrySide chainThiophenePolythiophenesPolythiopheneOrganic chemistryAnthraquinone
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