Search results for "Conjugated system"

showing 10 items of 225 documents

Synthesis of Microporous Carbon Nanofibers and Nanotubes from Conjugated Polymer Network and Evaluation in Electrochemical Capacitor

2009

One-dimensional fibers and tubes are constructed through the oriented carbon-carbon cross-linking reactions towards rigid conjugated polymer networks. As the result, a template-free and one-step synthesis of CNTs and CNFs is achieved through a simple carbonization of the as-formed carbon-rich tubular and fiberlike polyphenylene precursors under argon. Microporous CNTs and CNFs with a surface area up to 900 m2 g–1 are obtained, together with HR-TEM characterizations indicating the formation of intrinsic microporous structure in these rigid carbon-rich networks. The primary electrochemical experiments reveal their promising applications as advanced electrodes in electrochemical double-layered…

chemistry.chemical_classificationMaterials scienceCarbonizationCarbon nanofiberMicroporous materialPolymerCarbon nanotubeConjugated systemCondensed Matter PhysicsElectrochemistryElectronic Optical and Magnetic Materialslaw.inventionBiomaterialsChemical engineeringchemistrylawElectrodeElectrochemistryComposite materialAdvanced Functional Materials
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The folding of individual conjugated polymer chains during annealing.

2011

chemistry.chemical_classificationMaterials scienceChemical engineeringchemistryAnnealing (metallurgy)Polymer chemistryGeneral ChemistryPolymerConjugated systemCatalysisAngewandte Chemie (International ed. in English)
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New n-dopable thiophene based polymers

1999

Abstract New conjugated polymers containing variable amounts of thienyl and thienyl-S,S-dioxide units have been prepared by chemical or electrochemical polymerization of the appropriate substrates. The presence of the thienyl S,S-dioxide units leads to the decrease of the LUMO energies with respect to those of the ‘all thienyl’ counterparts. Electrochemical and spectro electrochemical data of n-doping of these materials are reported.

chemistry.chemical_classificationMaterials scienceElectrochemical polymerizationMechanical EngineeringMetals and AlloysPolymerConjugated systemCondensed Matter PhysicsPhotochemistryElectrochemistryElectronic Optical and Magnetic MaterialsElectrochemical dopingchemistry.chemical_compoundchemistryMechanics of MaterialsMaterials ChemistryThiopheneHOMO/LUMOSynthetic Metals
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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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Defects and defect engineering in Soft Matter.

2020

Soft matter covers a wide range of materials based on linear or branched polymers, gels and rubbers, amphiphilic (macro)molecules, colloids, and self-assembled structures. These materials have applications in various industries, all highly important for our daily life, and they control all biological functions; therefore, controlling and tailoring their properties is crucial. One way to approach this target is defect engineering, which aims to control defects in the material's structure, and/or to purposely add defects into it to trigger specific functions. While this approach has been a striking success story in crystalline inorganic hard matter, both for mechanical and electronic properti…

chemistry.chemical_classificationMaterials scienceNanotechnology02 engineering and technologyGeneral ChemistryPolymerConjugated system010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsBranching (polymer chemistry)01 natural sciences0104 chemical sciencesSupramolecular polymerschemistryLiquid crystalDendrimerAmphiphileSoft matter0210 nano-technologySoft matter
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Relationship between structure and electroluminescence of oligo(p-phenylenevinylene)s

1998

The preparation of LEDs with poly(p-phenylenevinylene) (PPV) as emitting material is well established, However, due to the presence of a distribution of conjugated chain lengths in the polymer, systematic investigations of the electroluminescence with polymeric materials are difficult, as far as the optical emission is concerned. We are studying the relationship between structural variation of substituted oligo(p-phenylenevinylene)s and their electroluminescent behaviour using a series of distyrylbenzenes with a variety of substituents in order to investigate their influence on the electroluminescence (EL). Furthermore, we synthesized a homologous series of monodisperse oligo(2,5-dipropoxy-…

chemistry.chemical_classificationMaterials sciencePhotoluminescenceOrganic ChemistryPolymerConjugated systemElectroluminescencePhotochemistryOligomerAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsInorganic Chemistrychemistry.chemical_compoundHomologous seriesMonomerchemistryPolymer chemistryPolystyreneElectrical and Electronic EngineeringPhysical and Theoretical ChemistrySpectroscopyOptical Materials
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Polymerization of mono- and multilayer forming diacetylenes

1977

Heptadeca-2,4-diine-1-ol and Heptadeca-2,4-diine-1-acid were synthesized and their polymerization behaviour in the solid state was investigated. Both compounds polymerize thermally below the melting point and photochemically under the action of uv-light to form polymers via 1,4-addition to the conjugated triple bonds with a backbone of conjugated double-and triple-bonds. The photoresponse spectra resemble the absorption spectra exhibiting maxima of photoreactivity in the absorption band of the conjugated triple bonds of the monomers.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsAbsorption spectroscopyPolymerConjugated systemPhotochemistryTriple bondchemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryPolymerizationAbsorption bandMaterials ChemistryMelting pointPhysical and Theoretical ChemistryColloid and Polymer Science
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Some monomers, oligomers and polymers with conjugated triple bonds

1991

In the first part new monoaminodiacetylenes with different numbers of CH2-groups, the formation of Perowskit-type Mn complexes and their polymerizability are described. Symmetrical diaminodiacetylenes and some derivatives therefrom have also been prepared. The second part deals with different types of polymers with diacetylene units in the backbone. Under irradiation color formation and crosslinking take place. Well-defined low molecular weight model compounds of polydiacetylenes is the subject of the third part. Finally rod-like but soluble polymers with alternating p-phenylene and acetylene units are described.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsDiacetyleneOrganic ChemistryPolymerConjugated systemCondensed Matter PhysicsTriple bondchemistry.chemical_compoundMonomerchemistryAcetylenePolymer chemistryMaterials ChemistryColor formationPolydiacetylenesMakromolekulare Chemie. Macromolecular Symposia
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Theoretical Design of Organic Metals Based on the Phthalocyanine Macrocycle

1990

Phthalocyanine molecular crystals and cofacially linked polymers are well documented as low-dimensional materials that may attain high electrical conductivities. Air-stable conductivities on the order of 1 to 1000 S/cm after partial oxidation by iodine have been reported.1–3 These conductivity studies indicate that the electrical conductivity has very little dependence on the identity of the atom complexed in the cavity, but is strongly dependent on the orientation and spacing of the phthalocyanine rings. A columnar stacking with minimum spacing leads to a maximum interaction between π-molecular orbitals on adjacent rings and promotes the highest conductivity. More effective π-interactions …

chemistry.chemical_classificationMaterials scienceStackingPolymerConductivityConjugated systemPhotochemistrychemistry.chemical_compoundCrystallographychemistryAtomic orbitalElectrical resistivity and conductivityPhthalocyanineMolecule
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“Click” on PLGA-PEG and hyaluronic acid: Gaining access to anti-leishmanial pentamidine bioconjugates

2017

Pentamidine (Pent), an antiparasitic drug used for the treatment of visceral leishmaniasis, has been modified with terminal azide groups and conjugated to two different polymer backbones (PLGA-PEG [PP] copolymer and hyaluronic acid [HA]) armed with alkyne end-groups. The conjugation has been performed by Copper Catalyzed Azido Alkyne Cycloaddition (CuAAC) using CuSO4 /sodium ascorbate as metal source. The novel PP-Pent and HA-Pent bioconjugates are proposed, respectively, as non-targeted and targeted drug delivery systems against Leishmania infections. Moreover, Pent has been encapsulated into PP nanoparticles by the oil-in-water emulsion method, with the aim to compare the biological activ…

chemistry.chemical_classificationMaterials sciencebiologyBiomedical EngineeringAlkyneBiological activity02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnologybiology.organism_classification01 natural sciencesCombinatorial chemistry0104 chemical sciencesBiomaterialschemistry.chemical_compoundchemistryTargeted drug deliveryHyaluronic acidmedicineAzideLeishmania infantum0210 nano-technologyPentamidinemedicine.drugJournal of Biomedical Materials Research Part B: Applied Biomaterials
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