Search results for "Conjugated polymers"

showing 10 items of 13 documents

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
researchProduct

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
researchProduct

Inherently fluorescent polyaniline nanoparticles in a dynamic landscape

2012

Abstract In this paper we report for the first time on the emissive behavior of two polyaniline (PANI) nanoparticle systems produced via oxidative chemical polymerization in the presence of either poly(vinyl alcohol) (PVA) or chitosan as polymeric stabilizers in water. The emission from PANI nanoparticles is irreversibly quenched by an increase of pH of the suspending medium from acid to neutral (chitosan–PANI) or alkaline (PVA–PANI). Conversely, PANI nanorods synthesized in the same conditions of the above, but in presence of poly(N-vinyl pyrrolidone), is not emissive at any pH. The role of the polymeric surfactant as a soft template is key in controlling the morphology and the properties …

Materials sciencePolymers and PlasticsPolyanilineGeneral Chemical EngineeringNanoparticlemacromolecular substancesConjugated polymersBiochemistryDispersion polymerizationchemistry.chemical_compoundNanoparticleDynamic light scatteringPolyanilinePolymer chemistryMaterials ChemistryEnvironmental ChemistryPhotoluminescence excitationPhotoluminescenceConductive polymerDispersion polymerizationConjugated polymers; Polyaniline; Nanoparticles; Dispersion polymerization; PhotoluminescenceConjugated polymertechnology industry and agricultureGeneral ChemistrychemistryChemical engineeringPolymerizationNanoparticlesNanorodSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
researchProduct

Long lived photoinduced charges in donor-acceptor anthraquinone substituted thiophene copolymers

2006

The photoinduced charge-transfer properties of a series of polyalkylthiophene copolymers, carrying anthraquinone substituents covalently linked to the conjugated backbone, have been studied in the solid state by photoinduced absorption (PA) and light-induced electron spin resonance (LESR) spectroscopy. The measurements indicate the formation of metastable charges arising from the photoinduced electron transfer from the polythiophene backbone to the anthraquinone moieties. At low temperatures (below 200 K), long-lived persistent charges are formed, exhibiting lifetimes that extend for several minutes; their recombination kinetics has been studied by following the formation and decay of the P…

ChemistrySettore CHIM/06 - Chimica OrganicaConjugated systemPhotochemistryAcceptorAnthraquinonePhotoinduced electron transferSurfaces Coatings and Filmslaw.inventionPhotoexcitationchemistry.chemical_compoundlawMaterials ChemistryThiopheneconjugated polymersPolythiophenePhysical and Theoretical ChemistryElectron paramagnetic resonancephotophysics
researchProduct

Organoboron Polymers for Photovoltaic Bulk Heterojunctions

2010

SOLAR-CELLSphotovoltaic bulk heterojunctionORGANIC PHOTOVOLTAICSn-type polymerthin filmsSOLAR-CELLS; ORGANIC PHOTOVOLTAICS; CONJUGATED POLYMERSCONJUGATED POLYMERSboranehigh performance polymer
researchProduct

Functionalization of P3HT with Various Mono- and Multidentate Anchor Groups

2018

Due to its favorable optoelectronic properties and the accessibility via Grignard metathesis (GRIM) polymerization, poly(3-hexylthiophene) (P3HT) is one of the most applied conjugated polymers. The ‘living' nature of GRIM polymerization enables the modification of the polymer and the installation of desired properties. In the present study, two versatile approaches for the synthesis of anchor group-modified P3HT have been developed, which enable the functionalization of various inorganic nanoparticles. Depending on the polymerization conditions, mono- and bifunctional ethynyl-terminated P3HT or solely monofunctionalized aldehyde-terminated P3HT was synthesized. Afterwards, the quantitative …

chemistry.chemical_classificationhybrid nanocompositesChemistryImineGeneral ChemistryPolymerConjugated systemGRIMMetathesisP3HTchemistry.chemical_compoundPolymerizationPolymer chemistryclick chemistryClick chemistryconjugated polymersSurface modificationBifunctional
researchProduct

New amphiphilic conjugates of mono- and bis(carboxy)-PEG(2,000) polymers with lipoamino acids as surface modifiers of colloidal drug carriers

2010

chemistry.chemical_classificationamphiphilesPolymers and Plasticspoly(ethylene glycol)Organic Chemistrylipoaminoacids copolymers surface modifiers drug carrierslipoamino acidslong-circulating drug-delivery systemsPolymerCondensed Matter PhysicsColloidMatrix-assisted laser desorption/ionizationchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPolymer chemistryAmphiphileamphiphiles; conjugated polymers; lipoamino acids; long-circulating drug-delivery systems; MALDI-TOF MS; poly(ethylene glycol)Materials Chemistryconjugated polymersMALDI-TOF MSPhysical and Theoretical ChemistryDrug carrierConjugate
researchProduct

Tailored conjugated polymer Langmuir-Schafer thin films in sensing transistors

2004

Organic Thin Film Transistors (OTFTs) have been fabricated, in a standard bottom gate configuration, with Langmuir-Schäfer (LS) or cast thin films of regioregular poly[1,4-(2,5-dioctyloxyphenylene)-2,5-thiophene], synthesized via an organometallic protocol, as active layers. The transistors electrical characterization has evidenced that LS based devices exhibit better performance level than cast film ones. Appealing perspectives for newly substituted conjugated polymers in OTFT sensing devices are discussed.

Conductive polymerchemistry.chemical_classificationLangmuirMaterials sciencebusiness.industryTransistorElectrical engineeringPolymerConjugated systemConjugated polymers Aromatic compounds cyclic voltammetryActive layerlaw.inventionchemistrylawThin-film transistorOptoelectronicsThin filmbusinessSPIE Proceedings
researchProduct

Donor-acceptor “double-cable” polythiophene with tunable acceptor content

2004

PhotovoltaicsOrganic Solar CellsConjugated Polymers
researchProduct

Polymorphism-Triggered Reversible Thermochromic Fluorescence of a simple 1,8-Naphthyridine

2013

The fluorescent behavior in the solid state of a naphthyridine-based donor–acceptor heterocycle is presented. Synthesized as a crystalline blue-emissive solid (Pbca), the compound can easily be transformed in its P21/c polymorphic form by heating. The latter material shows blue to cyan emission switching triggered by a reversible thermally induced phase transformation. This fact, the reversible acidochromism, and the strong anisotropic fluorescence of the compound in the solid state, account for the potential of 1,8-naphthyridines as simple and highly tunable organic compounds in materials science.

ThermochromismnaphthyridinesChemistryStereochemistryfield-effect transistorsSolid-statefood and beverageschemical sensorsGeneral ChemistrylassersCondensed Matter PhysicsFluorescenceCombinatorial chemistrysolid-state fluorescencePolymorphism (materials science)emissionconjugated polymersluminescencepackingGeneral Materials ScienceLuminescencephotocromism
researchProduct