Search results for "Radical"

showing 10 items of 1401 documents

A chiral molecular conductor: synthesis, structure, and physical properties of [ET]3[Sb2(L-tart)2].CH3CN (ET = bis(ethylendithio)tetrathiafulvalene; …

2004

The salt [ET](3)[Sb(2)(L-tart)(2)].CH(3)CN (1) has been obtained by electrocrystallization of the organic donor bis(ethylendithio)tetrathiafulvalene (ET or BEDT-TTF) in the presence of the chiral anionic complex [Sb(2)(L-tart)(2)](2-) (L-tart = (2R,3R)-(+)-tartrate). This salt crystallizes in the chiral space group P2(1)2(1)2(1) (a = 11.145(2) angstroms, b = 12.848(2) angstroms, c = 40.159(14) angstroms, V = 5750.4(14) angstroms(3), Z = 4) and is formed by alternating layers of the anions and of the organic radicals in a noncentrosymmetric alpha-type packing. This compound shows a room temperature electrical conductivity of approximately 1 S.cm(-1) and semiconducting behavior with an activa…

chemistry.chemical_classificationAntimonyChemistryStereochemistryRadicalMolecular ConformationTemperatureSalt (chemistry)Activation energyTartrateCrystallography X-RayMagnetic susceptibilityInorganic Chemistrychemistry.chemical_compoundCrystallographyElectrical resistivity and conductivityElectrochemistryOrganometallic CompoundsThermodynamicsPhysical and Theoretical ChemistryElectronic band structureTartratesTetrathiafulvaleneInorganic chemistry
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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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Lentils enhance probiotic growth in yogurt and provide added benefit of antioxidant protection

2013

Abstract We evaluated the antioxidant potential of lentil polysaccharides in stimulating the growth of probiotic bacteria in yogurt. Microbial counts, pH and total titratable acidity (TTA) were measured in yogurt samples containing starter cultures with or without probiotic bacteria, supplemented with whole ground green lentils. Additionally, the antioxidant potential of polysaccharides extracted from green, red, and dehulled red lentils were measured by oxygen radical absorbance capacity (ORAC) assay. Results demonstrate that green lentils selectively enhanced the number of probiotic bacteria in yogurt in the initial stages of storage and maintained overall microbial counts (starter cultur…

chemistry.chemical_classificationAntioxidantOxygen radical absorbance capacitymedicine.medical_treatmentfood and beveragesTitratable acidBiologyPolysaccharidelaw.inventionProbioticchemistry.chemical_compoundStarterLactobacillus acidophiluschemistrylawmedicineTroloxFood scienceFood ScienceLWT - Food Science and Technology
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Cyclodextrins in polymer synthesis: photocrosslinkable films via free radical copolymerization of methylated β-cyclodextrin-complexed styrene with so…

2001

The copolymerization of a methylated-β-cyclodextrin (m-β-CD) 1:1 host-guest compound of styrene (1a) with various molar ratios of sodium 4-(acrylamido)-phenyldiazosulfonate (2) is described. The copolymerization of complex 1a with 2 was carried out in water with 2,2′-azobis(N,N′-dimethyleneisobutyramidine)-dihydrochloride as the free radical initiator at 40°C. Depending on the amount of 2 incorporated in the copolymer, water- or DMF-soluble copolymers of high molar mass were obtained. Irradiation of the copolymers with UV light in solution resulted in rapid decomposition of the azo chromophore, and irradiation of the polymers as films led to crosslinking and thus to insolubility.

chemistry.chemical_classificationAqueous solutionMolar massMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringGeneral ChemistryPolymerInclusion compoundStyrenechemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerRadical initiatorDesigned Monomers and Polymers
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Solution Properties and Potential Biological Applications of Zwitterionic Poly(ε-N-methacryloyl-l-lysine)

2013

Poly(e-N-methacryloyl-l-lysine) (PMALys) was synthesized by free radical polymerization yielding a zwitterionic polymer with Mw = 721 000 g mol–1. The polymer dissolves in pure water as well as in aqueous salt solution up to 5 M NaClO4 and over wide range of pH values (1.3 ≤ pH ≤ 12.7) as single chains without any sign for aggregate formation. The zwitterionic polymer shows an expanded random coil structure at and close to isoelectric conditions and further expands upon addition of acid and base, respectively. The polymer fulfills four major prerequisites for a promising nano carrier in potential biomedical applications: (1) It is biocompatible, indicated by a low cytotoxicity. (2) It does …

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryLysineRadical polymerizationPolymerRandom coilInorganic ChemistryIsoelectric pointPolymer chemistryMaterials ChemistryAcid–base reactionCytotoxicityMacromolecules
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Structural Characterization of Glycoconjugate Polystyrene in Aqueous Solution

1999

Maltopentaose-carrying polystyrene was synthesized by the homopolymerization of vinylbenzyl maltopentaose amide. Resulted amphiphilc polymacromonomer was dissolved in 0.1 M urea aqueous solution, and its structure was characterized by small-angle X-ray scattering and molecular modeling. Maltopentaose-carrying polystyrene polymacromonomer was found to be represented by a molecular bottlebrush, composed of a large helix of polystyrene backbone and maltopentaose brushes. The molecular bottlebrush seems to be distributed randomly or many even be broken once or twice in segments with no apparent intersegmental spatial correlation. A large helix of polystyrene backbone is formed by a random seque…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsMolecular modelGlycoconjugateOrganic ChemistryRadical polymerizationInorganic Chemistrychemistry.chemical_compoundAldosechemistryAmidePolymer chemistryMaterials ChemistryUreaPolystyreneMacromolecules
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Suppression of new particle formation from monoterpene oxidation by NO<sub>x</sub>

2014

Abstract. The impact of nitrogen oxides (NOx = NO + NO2) on new particle formation (NPF) and on photochemical ozone production from real plant volatile organic compound (BVOC) emissions was studied in a laboratory setup. At high NOx conditions ([BVOC] / [NOx] < 7, [NOx] > 23 ppb) new particle formation was suppressed. Instead, photochemical ozone formation was observed resulting in higher hydroxyl radical (OH) and lower nitrogen monoxide (NO) concentrations. When [NO] was reduced back to levels below 1 ppb by OH reactions, NPF was observed. Adding high amounts of NOx caused NPF to be slowed by orders of magnitude compared to analogous experiments at low NOx conditions ([NOx] ~300 ppt)…

chemistry.chemical_classificationAtmospheric Science010504 meteorology & atmospheric sciencesMonoterpeneRadicalPhotodissociation010501 environmental sciencesRate-determining stepPhotochemistry01 natural sciencesOrganic compoundchemistry.chemical_compoundchemistry13. Climate actionParticleHydroxyl radicalNOx0105 earth and related environmental sciencesAtmospheric Chemistry and Physics
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A Versatile Grafting-to Approach for the Bioconjugation of Polymers to Collagen-like Peptides Using an Activated Ester Chain Transfer Agent

2009

DepartmentofMaterials Science and Engineering, University of Delaware, 201DuPont Hall, Newark, Delaware 19716,Received February 24, 2009Revised Manuscript Received April 24, 2009Biohybrid materials consisting of synthetic polymers andbiological moieties have gained more and more interest in therecent years.

chemistry.chemical_classificationBioconjugationPolymers and PlasticsChemistryScience and engineeringOrganic ChemistryRadical polymerizationChain transferPolymerGraftingInorganic Chemistrychemistry.chemical_compoundChemical couplingMaterials ChemistryPeptide synthesisOrganic chemistryMacromolecules
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Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography.

2009

During the last decades polymer-based nanomedicine has turned out to be a promising tool in modern pharmaceutics. The following article describes the synthesis of well-defined random and block copolymers by RAFT polymerization with potential medical application. The polymers have been labeled with the positron-emitting nuclide fluorine-18. The polymeric structures are based on the biocompatible N-(2-hydroxypropyl)-methacrylamide (HPMA). To achieve these structures, functional reactive ester polymers with a molecular weight within the range of 25,000-110,000 g/mol were aminolyzed by 2-hydroxypropylamine and tyramine (3%) to form (18)F-labelable HPMA-polymer precursors. The labeling procedure…

chemistry.chemical_classificationBiodistributionAcrylamidesFluorine RadioisotopesPolymers and PlasticsPolymersRadical polymerizationSize-exclusion chromatographyRadiochemistryBioengineeringChain transferPolymerPolymerizationRatsBiomaterialsPolymerizationchemistryIsotope LabelingPositron-Emission TomographyPolymer chemistryMaterials ChemistryAnimalsReversible addition−fragmentation chain-transfer polymerizationPreclinical imagingBiotransformationBiomacromolecules
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Functionalization of TiO2Nanoparticles with Semiconducting Polymers Containing a Photocleavable Anchor Group and Separation via Irradiation Afterward

2014

The controlled radical polymerization (RAFT polymerization) of semiconducting polymers based on poly(4,4′-dimethyl-triphenylamine) is described. These polymers are afterward end-functionalized with a photocleavable group and an anchor unit (catechol) for oxidic nanoparticles (NPs). Serving as a reference, polystyrene oligomers with the same end groups are also synthesized. Using these polymers allows functionalization of the TiO2-NPs, leading to an improved solubility and miscibility in organic solvents or polymer matrices. Irradiation in the UV region is used to split the photocleavable group and remove the polymer chains from the NPs, which leads to their aggregation.

chemistry.chemical_classificationCatecholPolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureNanoparticlePolymerCondensed Matter PhysicsMiscibilitychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationPolystyrenePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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