Search results for "Radical"

showing 10 items of 1401 documents

A new approach for the synthesis of magnetic materials based on nitroxide free radicals and inorganic coordination polymers

2001

The use of nitronyl nitroxide (NN) radicals as spectators inside extended inorganic magnetic lattices is described. Two possibilities are presently being explored, namely, the design of oxalato-bridged bimetallic networks by using cationic NN radicals of the N-alkylpyridinium type as templating agents, and the design of bimetallic lattices based on hexacyanometalates and nickel(II) diaminocomplexes incorporating anionic NN radicals of the carboxyphenyl type.

chemistry.chemical_classificationNitroxide mediated radical polymerizationMolecular magnetsRadicalCationic polymerizationchemistry.chemical_elementPolymerPhotochemistryInorganic ChemistryNickelchemistryMaterials ChemistryPhysical and Theoretical ChemistryBimetallic stripPolyhedron
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Functionalization of aliphatic polyesters by nitroxide radical coupling

2014

Functionalized poly(butylene succinate) (PBS) samples were prepared by a post-polymerization method based on the coupling reaction between TEMPO derivatives bearing different functionalities and PBS macroradicals generated by H-abstraction using a peroxide. 4-Benzoyloxy-2,2,6,6-tetramethylpiperidine-1- oxyl (BzO-TEMPO) and 4-(1-naphthoate)-2,2,6,6-tetramethylpiperidine-1-oxyl (NfO-TEMPO), a pro-fluorescent nitroxide, were successfully grafted on PBS, as revealed by MALDI TOF MS and UV-Vis spectroscopy. The functionalization degrees were accurately determined by UV-Vis analysis and confirmed by 1H-NMR spectroscopy. The grafting site was identified by combining theoretical calculations with e…

chemistry.chemical_classificationNitroxide mediated radical polymerizationgenetic structuresPolymers and PlasticsOrganic ChemistrySide reactionBioengineeringPolymerBiochemistryPeroxideCoupling reactionlaw.inventionPolyesterchemistry.chemical_compoundaliphatic polyesterchemistrylawPolymer chemistrySurface modificationElectron paramagnetic resonancenitroxide radicalpolymer functionalizationPolymer Chemistry
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Vibronic structure in triatomic molecules : The hydrocarbon flame bands of the formyl radical (HCO). A theoretical study

1998

A theoretical study of the vibrational structure of the math 2A′ ground and math 2A′ excited states of the formyl radical, HCO, and its deuterated form, DCO, has been performed. The potential energy surfaces have been computed by means of a multiconfigurational perturbative method, CASPT2. The computed geometries and the harmonic and anharmonic frequencies are successfully compared to the available experimental information. The vibrational intensities of the transition math 2A′↔math 2A′ have been computed both for absorption and emission. The results lead to accurate determinations of several structural parameters and some reassignments of the vibrational transitions of the so-called hydroc…

chemistry.chemical_classificationOrganic compounds ; Free radicals ; Potential energy surfaces ; Vibronic states ; Vibrational statesChemistryTriatomic moleculeAnharmonicityGeneral Physics and AstronomyFree radicalsVibronic statesPotential energyUNESCO::FÍSICA::Química físicaHydrocarbonDeuteriumExcited statePotential energy surfacesOrganic compoundsVibrational statesPhysical and Theoretical ChemistryAbsorption (chemistry)Atomic physicsPhysics::Chemical Physics:FÍSICA::Química física [UNESCO]Astrophysics::Galaxy Astrophysics
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Surface coatings based on polysilsesquioxanes: Grafting-from approach starting from organic polymers

2009

AbstractPoly(methylsilsesquioxane) (PMSSQ) based hybrid materials are promising candidates to produce substrate-independent stable and adherent surface coatings. Usually these materials are synthesized by controlled radical polymerization from inorganic precursors. The presented synthetic pathway in here demonstrates how to graft PMSSQ networks from an endgroup-functionalized organic polymer and thus enlarges the range of accessible inorganic/organic hybrid coating materials.

chemistry.chemical_classificationOrganic polymerMaterials sciencechemistryChemical engineeringRadical polymerizationCoating materialsPolymer chemistryPolymerGraftingHybrid materialMicrobiologySol-gel
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Does catalase play a role in Adriamycin induced cardiotoxicity?

1980

Summary Adriamycin causes an increase of lipid peroxidation in mouse cardiac homogenates that is dependent on the concentration of the antiblastic. The same phenomenon is not observed in the hearts of mice treated with an elevated dose of Adriamycin in which, conversely, an increase of the antioxidizing enzyme catalase was noticed. The significance of these findings is discussed with relationship to the hypothesis of an enhanced free radicals formation at the basis of Adriamycin induced cardiotoxicity.

chemistry.chemical_classificationPharmacologyCardiotoxicityLipid PeroxidesbiologyFree RadicalsHeart DiseasesMyocardiumPharmacologyNADCatalaseMalonatescarbohydrates (lipids)Lipid peroxidationchemistry.chemical_compoundMiceEnzymechemistryCatalaseDoxorubicinMalondialdehydepolycyclic compoundsbiology.proteinAnimalsFemalePharmacological Research Communications
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1984

Influence de la structure de chaine sur le type de phase et relation entre la masse moleculaire et les temperatures de transition

chemistry.chemical_classificationPhase transitionChemistryLiquid crystalTransition temperaturePhase (matter)Radical polymerizationPolymer chemistrySolution polymerizationPolymerMethacrylateDie Makromolekulare Chemie, Rapid Communications
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1984

chemistry.chemical_classificationPhase transitionMembraneDeuteriumChemical engineeringLiquid crystalChemistryPhase (matter)Radical polymerizationOrganic chemistryMoleculePolymerDie Makromolekulare Chemie, Rapid Communications
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Synthesis, crystallographic and spectroscopic characterization and magnetic properties of dimer and monomer ternary copper(II) complexes with sulfona…

2010

Abstract Three dinuclear and one mononuclear copper(II)-1,10-phenanthroline ternary complexes, [Cu(L1)(phen)(OH)]2 (1), [Cu(L2)(phen)(OH)]2·3H2O (2), [Cu(L3)(phen)(OH)]2 (3) and [Cu(L4)2(phen)(H2O)] (4), with thiadiazole sulfonamide derivative ligands: HL1 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)naphthalene-1-sulfonamide), HL2 (N-(5-ethylthio)-1,3,4-thiadiazol-2-yl)-4-methylbenzenesulfonamide), HL3 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide) and HL4 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)-4-methylbenzenesulfonamide) have been synthesized and characterized. In the four complexes each copper atom is five-coordinated. The structure of complexes 1, 2 and 3 consists of a dimeric unit with a C2 sy…

chemistry.chemical_classificationPhenanthrolineDimerchemistry.chemical_elementCleavage (embryo)Ascorbic acidCopperSulfonamideInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistryMaterials ChemistryHydroxyl radicalPhysical and Theoretical ChemistryPolyhedron
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Evidence for chain transfer in the atom transfer radical polymerization of butyl acrylate

2000

Poly(butyl acrylate) (PBuA) of high molecular weight was synthesized by atom transfer radical polymerization (ATRP) in ethyl acetate. Whereas for low molecular weight polymers, a linear increase of the number-average molecular weight. M n , versus conversion and narrow molecular weight distributions indicate the suppression of side reactions, a downward curvature in the plot of M n versus conversion was observed for high molecular weights (M n > 50 000). This effect is explained by chain transfer reactions, leading to branched polymers. GPC measurements with a viscosity detector give evidence for the branched structure of high molecular weight polymers obtained in ATRP. In addition, transfe…

chemistry.chemical_classificationPolymers and PlasticsAtom-transfer radical-polymerizationButyl acrylateOrganic ChemistryRadical polymerizationChain transferSolution polymerizationPolymerchemistry.chemical_compoundMonomerchemistryCatalytic chain transferPolymer chemistryMaterials ChemistryMacromolecular Rapid Communications
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Patterning of a Surface Immobilized ATRP Initiator with an Inkjet Printer

2010

A new technique for patterning polymer brushes on the micrometer scale has been developed in which an inkjet printer was used to deposit droplets of acid on a surface-immobilized initiator for atom transfer radical polymerization (ATRP). The acid cleaved an ester bond in the ATRP initiator in a saponification reaction. As a result, the ATRP initiator was rendered inactive. To control the degree of defunctionalization, a new initiator containing a weak ester bond was derived from a tertiary alcohol. Comparison to an established ATRP initiator, derived from a primary alcohol, showed that the novel initiator was defunctionalized with a higher efficiency. Control of the reaction time allowed to…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationChemistryAtom-transfer radical-polymerizationOrganic ChemistryAlcoholPolymerPrimary alcoholGraftingInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryMoleculeSaponificationMacromolecules
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