Search results for "Conjugated system"

showing 10 items of 225 documents

Intercorrelation between Structural Ordering and Emission Properties in Photoconducting Polymers

2009

We investigated the structural properties of anthracene containing poly(p-phenylene−ethynylene)-alt-poly(p-phenylene−vinylene) polymers with general constitutional unit: (−Ph−C≡C−Anthr−C≡C−Ph−CH═CH−Ph−CH═CH−)n by means of wide-angle X-ray scattering and fluorescence spectroscopy. Interchain interactions were systematically modified by decorating the conjugated polymer backbone with linear or branched or combinations of linear and branched alkoxy side chains. Special emphasis is taken on an evaluation method for fiber scattering spectra that allows the deduction of important structural details of polymer materials with limited degree of order. These include positional correlations along the …

chemistry.chemical_classificationAnthraceneMaterials sciencePolymers and PlasticsScatteringOrganic ChemistryStackingPolymerConjugated systemFluorescence spectroscopyInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryAlkoxy groupSide chainMacromolecules
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[39] Lipoperoxyl radical-scavenging activity of vitamin A and analogs in homogeneous solution

1994

Publisher Summary This chapter describes the assay method for determining the reactivity of all- trans -retinol and other natural and synthetic retinoids, with radicals generated by reaction of the lipid-soluble azo initiator 2,2 ' -azobis(2,4-dimethylvaleronitrile) (AMVN) with methyl linoleate. The chapter discusses the general principles for measuring antioxidant activity. The oxidation of linoleic acid methyl ester (LAME) is the simplest model for studying the oxidation of polyunsaturated lipids and has been widely adopted to evaluate antioxidant activity. Because linoleic acid has two double bonds, peroxidation occurs at the bisallylic hydrogens and generates conjugated diene hydroperox…

chemistry.chemical_classificationAntioxidantDouble bondLinoleic acidmedicine.medical_treatmentRadicalSubstrate (chemistry)Conjugated systemchemistry.chemical_compoundchemistryLipid oxidationmedicineOrganic chemistryReactivity (chemistry)
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On-Surface Synthesis of Oligo(indenoindene)

2020

Fully conjugated ladder polymers (CLP) possess unique optical and electronic properties, and are considered promis-ing materials for applications in (opto)electronic devices. Poly(indenoindene) is a CLP consisting of an alternating array of five- and six-membered rings, which has remained elusive so far. Here, we report an on-surface synthesis of oligo(indenoindene) on Au(111). Its structure and a low elec-tronic bandgap have been elucidated by low-temperature scanning tunneling microscopy and spectroscopy and non-contact atomic force microscopy, complemented by density functional theory calculations. Achieving defect-free seg-ments of oligo(indenoindene) offers an exclusive insight into th…

chemistry.chemical_classificationBand gapAtomic force microscopy530 PhysicsElectronic bandNanotechnologyGeneral ChemistryPolymerConjugated system010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceslaw.inventionColloid and Surface Chemistrychemistrylaw540 ChemistryDensity functional theoryScanning tunneling microscopeSpectroscopy
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The effect of 2,2-dicyanovinyl groups as electron acceptors in push–pull substituted oligo(1,4-phenylenevinylene)s

2003

Abstract The newly synthesized oligo(1,4-phenylenevinylene) series 2a–d with bis(2-hexyloctyl)amino groups as electron donors and 2,2-dicyanovinyl groups as electron acceptors represents conjugated oligomers with strong push–pull effects. Due to the decrease of the intramolecular charge transfer with increasing numbers of repeat units (n=1–4), the long-wavelength transition shows a particularly great hypsochromic shift for the extension of the chromophore.

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryElectronConjugated systemChromophoreElectron acceptorBiochemistryMedicinal chemistryIntramolecular forceDrug DiscoveryHypsochromic shiftPush pullTetrahedron Letters
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Metal-organic frameworks conjugated with biomolecules as efficient platforms for development of biosensors

2021

Abstract Recent developments in the field of metal-organic frameworks (MOFs) have renewed the interests of scientists to bring about a major breakthrough in this field soon. These particles consist of ultra-highly porous and tremendous internal surface areas with extraordinary variabilities that make them highly potent compounds in nanomedicine. Moreover, low weight, large free volumes, and multiple functionalities of these particles have made them extremely attractive for various applications. Along with a critical role in the adsorption and separation of different analytes, they also have an immense role in the development of biosensor platforms that are expected to pave the way for accur…

chemistry.chemical_classificationComputer scienceBiomolecule010401 analytical chemistryNanotechnologyConjugated system01 natural sciences0104 chemical sciencesAnalytical ChemistrychemistryNanomedicineMetal-organic frameworkBiosensorSpectroscopyTrAC Trends in Analytical Chemistry
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High-Performance Electron-Transporting Polymers Derived from a Heteroaryl Bis(trifluoroborate)

2011

In this communication, we report that dipotassium aryl bis(trifluoroborate)s make stable and easy-to-purify yet reactive monomers under Suzuki polycondensation reactions. A bis(trifluoroborate) of 2-alkylbenzotriazole was prepared successfully and copolymerized with dibromobenzothiadiazole in the presence of a Pd catalyst and LiOH, yielding high molecular weight conjugated polymers. This polymer (P1) composed of all electron-accepting units shows excellent electron-transport properties (μ(e) = 0.02 cm(2) V(-1) s(-1)), which proves the value of the aryl bis(trifluoroborate) monomers and suggests that many other types of semiconducting polymers that could not be accessed previously can be syn…

chemistry.chemical_classificationCondensation polymerHalogenationTransistors ElectronicPolymersArylRespiratory electron transportGeneral ChemistryPolymerTriazolesConjugated systemBiochemistryCatalysisCatalysisElectron Transportchemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryBoratesPolymer chemistryJournal of the American Chemical Society
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Self-organized nanostructures of poly(4-vinylpyridine), polyaniline and polyamides due to metal complexation

2002

Comb-shaped supramolecules are constructed using flexible polymers and semi-rigid conjugated undoped or doped conjugated polymers upon complexing Zinc dodecyl benzene sulphonate, Zn(DBS) 2 . Self-organized nanostructures are formed in the bulk due to competing attractive interactions (coordination or water mediated hydrogen bonding) and repulsive polar/nonpolar interactions, showing characteristic long periods of ca. 30 A.

chemistry.chemical_classificationConductive polymerCOORDINATIONMaterials sciencePolymers and PlasticsHydrogen bondOrganic Chemistrychemistry.chemical_elementZincPolymerConjugated systemCondensed Matter PhysicsMetalchemistry.chemical_compoundchemistrySUPRAMOLECULAR POLYMERIC MATERIALSSYSTEMSvisual_artPolyanilinePolymer chemistryPolyamideComputingMethodologies_DOCUMENTANDTEXTPROCESSINGMaterials Chemistryvisual_art.visual_art_mediumGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)Macromolecular Symposia
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A spectroelectrochemical study of poly(dithienothiophenes)

1997

Abstract The use of n- and p-dopable conjugated polymers as both the working and counter electrodes in an electrochemical device has always attracted chemists and has stimulated the design of new molecules with a low energy gap that can be p- and n-doped efficiently. The present paper reports the spectroelectrochemical study of polymers obtained from several dithienothiophene isomers, molecules with three thiophene rings fused in different positions. Of the six isomers, poly(dithieno[3,4-b:3′,2′-d]thiophene) and poly(dithieno[3,4-b:2′,3′-d] thiophene) were tested against poly(dithieno[3,2-b:2′,3′-d]thiophene) and poly(dithieno[3,4-b:3′,4′-d]thiophene). The differences in their performance, …

chemistry.chemical_classificationConductive polymerGeneral Chemical EngineeringPolymerConjugated systemElectrochemistryAnalytical Chemistrychemistry.chemical_compoundLow energychemistryElectrodePolymer chemistryElectrochemistryThiopheneMoleculeJournal of Electroanalytical Chemistry
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Conjugate Alkynylation of Electrophilic Double Bonds. From Regioselectivity to Enantioselectivity

2018

This review surveys the historical efforts addressed toward the development of the conjugate alkynylation reaction. The regio- and enantioselective conjugate alkynylation of electron-deficient double bonds, most commonly unsaturated carbonyl compounds, has been an elusive reaction for a long time. Intensive research during the last decades has resulted in the identification of a number of effective reagents and catalysts to perform this reaction. Non-stereoselective conjugate alkynylation of unsaturated carbonyl compounds was first achieved by using preformed alkynyl organometallics and later with terminal alkynes under catalytic conditions. These methods paved the way for the development o…

chemistry.chemical_classificationDouble bond010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisRegioselectivityConjugated system010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisCatàlisiReagentElectrophileQuímica orgànicaConjugateSynthesis
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Determination of the absolute configuration of (−)-abietic acidviaits (4R,5R,9R,10R)-7,13-abietadien-18-ylp-bromobenzoate derivative

2006

The absolute configuration of the title bromo derivative of abietic acid, C27H35BrO2, has been determined. The structural analysis confirms the absolute stereochemistry for (−)-abietic acid proposed by Bose & Struck [(1959). Chem. Ind. (London), pp. 1628–1630] on the basis of optical rotatory dispersion measurements. The mol­ecule exhibits a trans anti 6/6/6 tricyclic hydro­carbon skeleton, with the cyclo­hexane ring in the expected chair form and the two cyclo­hexene rings, the double bonds of which are conjugated, in half-chair conformations.

chemistry.chemical_classificationDouble bondAbsolute configurationGeneral ChemistryConjugated systemCondensed Matter PhysicsRing (chemistry)Medicinal chemistrychemistry.chemical_compoundBenzoate derivativechemistryGeneral Materials ScienceAbietic acidOptical rotatory dispersionDerivative (chemistry)Acta Crystallographica Section E Structure Reports Online
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