Search results for "Triphenylamine"

showing 9 items of 29 documents

Determination of charge carrier mobility of hole transporting polytriarylamine-based diodes

2010

Hole transport properties of three different side chain poly(triarylamines) have been determined by means of the analysis of steady-state current-voltage characteristics using co-planar diode structures. The interpretation is based on space-charge limited models with field-dependent mobility. Mobilities between ~ 10- 8 and 10- 6 cm2 V- 1 s- 1 are obtained. The highest mobility is achieved for poly(tetraphenylbenzidine) devices and the lowest for poly(triphenylamine) devices. Electron-rich methoxy substituents increase the mobility of poly(triphenylamine)s. A comparison of the mobility values with those obtained using organic field-effect transistors is also given. © 2009 Elsevier B.V. All r…

Organic electronicsMobilityElectron mobilitybusiness.industryOrganic electronicsMetals and AlloysSurfaces and InterfacesPoly(triarylamines)TriphenylamineSpace chargeHole-transporting materialsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOrganic semiconductorchemistry.chemical_compoundchemistryTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYMaterials ChemistrySide chainOptoelectronicsField-effect transistorbusinessDiode
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Synthesis and photovoltaic performance of asymmetric di-anchoring organic dyes

2015

Abstract Two novel metal-free organic dyes bearing two asymmetric double donor–acceptor segments were synthesized. Their physical, optical, electrochemical properties and photovoltaic performances were investigated. Compared with the mono-anchoring dye containing single donor–acceptor chain, these new dyes exhibited a broader and much stronger absorption in the light wavelength ranging from 400 to 600 nm, showed higher IPCE values and short-circuit current density, which led to more efficient photovoltaic performance. The dye with triphenylamine and phenothiazine as two electron donors and two cyanoacrylic acids as two electron acceptors exhibited an impressive power conversion efficiency o…

Photocurrentchemistry.chemical_classificationMaterials scienceProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy conversion efficiencyElectron acceptorPhotochemistryElectrochemistryTriphenylaminechemistry.chemical_compoundDye-sensitized solar cellchemistryPhenothiazineAbsorption (electromagnetic radiation)Dyes and Pigments
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Greatly enhanced intermolecular π-dimer formation of a porphyrin trimer radical trications through multiple π bonds.

2010

A trefoil-like porphyrin trimer linked by triphenylamine (TPA-TPZn(3)) was synthesized. A three-electron oxidation of TPA-TPZn(3) forms a radical trication (TPA-TPZn(3)(3+)), in which each porphyrin ring undergoes a one-electron oxidation. The radical trication TPA-TPZn(3)(3+) spontaneously dimerizes to afford (TPA-TPZn(3))(2)(6+) in CH(2)Cl(2) . The characteristic charge-resonance band due to the charge delocalization over the π system of (TPA-TPZn(3))(2)(6+) was observed in the NIR region. The initial oxidation potential of TPA-TPZn(3) is negatively shifted relative to that of the corresponding monomer porphyrin, which results from the stabilization of the oxidized state of TPA-TPZn(3) as…

PorphyrinsMolecular StructureDimerOrganic ChemistryElectron Spin Resonance SpectroscopyTemperatureTrimerElectronsGeneral ChemistryPhotochemistryTriphenylaminePorphyrinCatalysislaw.inventionchemistry.chemical_compoundchemistryRadical ionlawStability constants of complexesCationsPi interactionElectron paramagnetic resonanceDimerizationOxidation-ReductionChemistry (Weinheim an der Bergstrasse, Germany)
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Hyper-Rayleigh scattering and two-photon luminescence of phenylamine- indandione chromophores

2012

Based on results of quantum chemical (QC) screening, we put under research several phenylamine indane-1,3-dione derivatives including octupolar NLO chromophore A3BI. According to these calculations, molecular first hyperpolarizability (βHRS) should be enhanced upon replacement of methyl substituents with phenyl groups. Surprisingly, βHRS values obtained in our measurements by hyper-Rayleigh scattering (HRS) are much higher than one could expect from QC. Bearing in mind that two-photon luminescence (TPL) is usual cause for overestimation of βHRS in HRS measurements, we have accomplished investigations of TPL properties of these compounds. All investigated triphenylamine derivatives exhibit s…

StereochemistryChemistryScatteringTwo photon luminescenceHyperpolarizabilityChromophorePhotochemistryTriphenylamineSpectral linesymbols.namesakechemistry.chemical_compoundsymbolsRayleigh scatteringLuminescenceIOP Conference Series: Materials Science and Engineering
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Light-induced demixing of hole or electron transporting moieties

2004

This paper describes the synthesis of two tri-phenylamine monomers (hole conducting) and one triazine monomer (electron conducting) which differ in their copolymerization parameters because of their styrene and vinyl ester nature. A blend of triphenylamine monomer and poly-(ethylene glycol) and mixtures of both types of monomers (triphepylamine and triazine) were illuminated through a line mask, creating laterally modulated radicals, thus leading to lateral demixing. The experiments with mixtures of triphenylamine and triazine monomers show that the concentration of p- or n-type polymers can be modulated laterally in a controlled way.

chemistry.chemical_classificationConductive polymerMaterials sciencePhotopolymerizationPolymers and PlasticsTriphenylamineOrganic ChemistryDemixingConducting polymersPolymerTriphenylaminePhotochemistrychemistry.chemical_compoundPhotopolymerMonomerTriazinechemistryPolymer chemistryMaterials ChemistryCopolymerEthylene glycolTriazine
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Functional templates for hybrid materials with orthogonal functionality.

2009

We demonstrate an integrated approach to prepare a nanostructured, multifunctional material with mutually exclusive, orthogonal properties. The hybrid material was obtained within a single step via self-assembly in solution. It consists of TiO(2) as a functional metal oxide and an amphiphilic block copolymer, poly(ethylene oxide)-b-poly(triphenylamine) (PEO-PTPA). Within the materials' synthesis, the block copolymer not only acts as a templating agent but also adds an electronic functionality to the resulting hybrid material. During the synthesis, a variety of self-assembled morphologies, ranging from spheres to wires, can be created. The obtained morphology depends on the weight fraction o…

chemistry.chemical_classificationMaterials scienceScanning electron microscopeOxideNanotechnologySurfaces and InterfacesPolymerCondensed Matter PhysicsTriphenylamineCrystallinitychemistry.chemical_compoundchemistryTransmission electron microscopyElectrochemistryCopolymerGeneral Materials ScienceHybrid materialSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Inversion of the Triphenylamine Molecule

1964

chemistry.chemical_compoundMaterials sciencechemistryMoleculeGeneral MedicineGeneral ChemistryTriphenylamineMolecular physicsInversion (discrete mathematics)CatalysisAngewandte Chemie International Edition in English
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Oligo(phenylenevinylene)s end-capped with phenothiazine or triphenylamine

2003

AbstractMonodisperse oligo(phenylenevinylene)s end-capped with arylamines have been prepared via Horner Olefinations from bisphosphonates and arylaminobenzaldehydes. The influences of the conjugation length, different arylamine end groups, and of side chains with various electronic character on the electrical and optical properties of the chromophores are investigated. The elongation of the π-conjugated segment from 3 to 5 rings gives rise to bathochromic shifts of the electronic spectra and a slight increase of the oxidation potential. The same but more pronounced is true when the central electron donating ethers are replaced by the strong acceptor alkylsulfone. The electronic spectra of c…

chemistry.chemical_compoundMaterials sciencechemistryPhenothiazineBathochromic shiftDispersitySide chainCopolymerChromophorePhotochemistryTriphenylamineAcceptorMRS Proceedings
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Pyridine-Incorporated Dihexylquaterthiophene: A Novel Blue Emitter for Organic Light Emitting Diodes (OLEDs)

2012

The synthesis and characterisation of 2,5-bis(5′-hexyl-[2,2′-bithiophen]-5-yl)pyridine (Th4PY) and its use as a blue emitter in organic light emitting diodes (OLEDs) is reported. Th4PY was synthesised in high yield using a straightforward Suzuki coupling route with commercially available starting materials. As Th4PY is both soluble and has low molecular weight, blue OLEDs were fabricated using both spin-coating and vacuum deposition thin film processing techniques to study the effect of processing on device performance. OLED devices using a spin-coated layer consisting of 4′,4′′-tris(N-carbazolyl)triphenylamine (TCTA) and 2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (PBD) as a …

chemistry.chemical_compoundVacuum depositionchemistrySuzuki reactionOLEDNanotechnologyGeneral ChemistryThin filmTriphenylamineLuminous efficacyLayer (electronics)Common emitterAustralian Journal of Chemistry
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