Search results for "Conjugated"

showing 10 items of 288 documents

[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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Synthesis and Photoluminescent Properties of 1,1‘-Binaphthyl-Based Chiral Phenylenevinylene Dendrimers

2003

New chiral, soluble binaphthyl derivatives that incorporate stilbenoid dendrons at the 6,6′-positions have been prepared. The synthesis of the new enantiopure dendrimers was performed in a convergent manner by Horner-Wadsworth-Emmons (HWE) reaction of the appropriately functionalized 1,1′-binaphthyl derivative (R)-1 and the appropriate dendrons (R)2nGn-CHO. Different electroactive units were incorporated in the peripheral positions of the dendrons in order to tune both the optical and electrochemical behavior of these systems. Fluorescence measurements on the chiral dendrimers reveal a strong emission with maxima between 409 and 508 nm depending upon the substitution pattern. Finally, t…

chemistry.chemical_classificationCatenaneOrganic ChemistrySettore CHIM/06 - Chimica OrganicaGeneral MedicineElectrochemistryPhotochemistryAldehydeCombinatorial chemistryChemical synthesisFluorescenceRedoxEnantiopure drugchemistryDendrimerCalixareneCyclic voltammetryConjugated DendrimersThe Journal of Organic Chemistry
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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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Intramuscular fatty acid composition of lambs given a tanniniferous diet with or without polyethylene glycol supplementation.

2007

The aim of this trial was to investigate the effects that dietary tannins have on lamb intramuscular fatty acids. Twenty-seven lambs were divided into three homogeneous groups: control group, receiving commercial concentrate based on maize; tannin group, fed a diet based on carob pulp (45% as fed basis); PEG group, receiving the same diet as the latter with addition of 42g/kg of polyethylene glycol (PEG, a binding agent that eliminates the effects of condensed tannins). The duration of the trial was 45 d. Intramuscular fatty acids were measured in the longissimus dorsi muscle. The isomer cis-9 trans-11 of linoleic acid (conjugated linoleic acid or CLA) and linolenic acid were higher in the …

chemistry.chemical_classificationChemistryLinolenic acidLinoleic acidConjugated linoleic acidLambVaccenic acidPolyethylene glycolFatty acidchemistry.chemical_compoundAnimal scienceBiochemistryPEG ratioCarob podTanninConjugated linoleic acidTanninsFood SciencePolyunsaturated fatty acid
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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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