Search results for " Radical polymerization"

showing 10 items of 51 documents

Polyoxometalate salts of cationic nitronyl nitroxide free radicals

2008

The cationic nitronyl nitroxide free radical of the N-methylpyridinium type p-MepyNN + has been combined with [Mo 8 0 26 ] 4- and Keggin [SiW 12 0 40 ] 4- polyanions to afford salts ( p-MepyNN) 4 [Mo 8 0 26 ] DMSO (DMSO = dimethylsulfoxide) (1) and (p-MepyNN)4[SiW 12 0 40 ] 6DMF (DMF = dimethylformamide) (2). Herein, their structural and magnetic properties are described.

Nitroxide mediated radical polymerizationChemistryMagnetismRadicalCationic polymerizationGeneral ChemistryCondensed Matter PhysicsPhotochemistrychemistry.chemical_compoundMetallatePolyoxometalatePolymer chemistryDimethylformamideGeneral Materials ScienceGroup 2 organometallic chemistrySolid State Sciences
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A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties

2020

An interaction of M(hfac)2 (M = Mn or Ni) with N-(bis(4,4,5,5-tetramethyl-3-oxido-1-oxyl-4,5-dihydro-1H-imidazol-2-yl)methylene)-2-methyl-propan-2-amine oxide (a nitronyl nitroxide diradical with theC[double bond, length as m-dash]N(O)-tert-Bu coupler) was investigated under various conditions. It was found that prolongation of reaction time caused transformation of the initial diradical into new diradicals with the uniqueC[double bond, length as m-dash]N-OH coupling unit and formation of binuclear Mn(ii) and Ni(ii) complexes, which were characterized by X-ray diffraction analysis. The resulting binuclear heterospin complexes have a complicated magnetic structure with six paramagnetic cente…

Inorganic ChemistryParamagnetismNitroxide mediated radical polymerizationCrystallographyMaterials scienceMagnetic structureDiradicalAb initio quantum chemistry methodsExchange interactionDensity functional theoryElectronic structureDalton Transactions
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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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2,2-Diphenylbenzo[c]quinoline-1-oxyl

2009

In the title compound, C25H18NO, a stable phenanthridinic nitroxide, the ring containing the nitroxide function assumes a twist-boat conformation and the dihedral angle formed by adjacent benzene rings is 21.78 (5)°. The phenyl substituents at position 2 are approximately orthogonal to each other, forming a dihedral angle of 81.04 (4)°. The crystal structure is stabilized by an intramolecular C—H...O hydrogen bond and by C—H...π interactions.

Nitroxide mediated radical polymerizationHydrogen bondQuinolineGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic Paperslcsh:Chemistrychemistry.chemical_compoundCrystallographylcsh:QD1-999chemistryGeneral Materials ScienceBenzeneActa Crystallographica Section E Structure Reports Online
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Contribution of Protein Flexibility to the Foaming Properties of Casein

1990

The effect of biopolymer flexibility on the foaming properties of casein was investigated. Flexibility was altered by: (1) chemical modification (covalent binding of a monosaccharide on the lysyl residues) or (2) pH change. Electron Spin Resonance was used to measure the reorientational frequency of casein residues labeled with nitroxide radicals. High levels of glycosylation induced increased protein flexibility and improved the foaming capacity. Good agreement was observed between higher values of flexibility and improved surface properties near the isoelectric point.

chemistry.chemical_classificationNitroxide mediated radical polymerizationGlycosylationFlexibility (anatomy)Chemical modificationengineering.materialchemistry.chemical_compoundmedicine.anatomical_structureIsoelectric pointChemical engineeringchemistryCaseinengineeringmedicineOrganic chemistryMonosaccharideBiopolymerFood ScienceJournal of Food Science
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Integrated experimental and computational spectroscopy study on the protonation of the α-nitronyl nitroxide radical unit

2011

The stability of the α-nitronyl nitroxide radical unit under acidic conditions is investigated by an integrated experimental UV/Vis spectroscopy and TDDFT study. In the field of molecular magnetism, α-nitronyl nitroxide radicals are important as purely organic spin carriers due to their synthetic versatility. Here, the existence of an intermediate of the protonated α-nitronyl nitroxide radical unit is demonstrated for the first time and a proposed disproportionation reaction is confirmed.

Models MolecularNitroxide mediated radical polymerizationFree RadicalsChemistryMagnetismSpectrum AnalysisRadicalMolecular ConformationGeneral Physics and AstronomyDisproportionationProtonationTime-dependent density functional theoryPhotochemistryCyclic N-OxidesQuantum TheoryProtonsPhysical and Theoretical ChemistrySpectroscopySpin (physics)Phys. Chem. Chem. Phys.
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Study of Atrp Process for the Grafting of Vinyl Monomers on PVC and PVDF

2014

STUDY OF ATRP PROCESS FOR THE GRAFTING OF VINYL MONOMERS ON PVC AND PVDF Sonia Lanzalaco, Onofrio Scialdone, Alessandro Galia, Rosalia Mauro, Flavia Lazzano Dipartimento di Ingegneria Chimica, Gestionale, Informatica, Meccanica, Viale delle Scienze, Palermo e-mail: sonia.lanzalaco@unipa.it ATRP (atom transfer radical polymerization) has been recently used to prepare graft copolymers with regularly-spaced polymer chains from polymeric macroinitiators that have pendant chemical groups containing radically transferable halogen atoms [1]. The halogen atom serves as initiation site for the polymerization of side chains. Furthermore, Matyjaszewsky and Gennaro showed that an externally applied ele…

atom transfer radical polymerization PVDF PVC
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Radical Polymerization of Styrene Controlled by Half-Sandwich Mo(III)/Mo(IV) Couples: All Basic Mechanisms Are Possible

2001

Density functional calculations of bond dissociation energies (BDEs) have been used as a guide to the choice of metal system suitable for controlling styrene polymerization by either the stable free radical polymerization (SFRP) or the atom transfer radical polymerization (ATRP) mechanism. In accord with the theoretical prediction, CpMo(eta(4)-C(4)H(6))(CH(2)SiMe(3))(2), 2, is not capable of yielding SFRP of styrene. Still in accord with theoretical prediction, CpMo(eta(4)-C(4)H(6))Cl(2), 1, CpMo(PMe(3))(2)Cl(2), 3, and CpMo(dppe)Cl(2) (dppe = 1,2-bis(diphenylphosphino)ethane), 4, yield controlled styrene polymerization by the SFRP mechanism in the presence of 2,2'-azobisisobutyronitrile (A…

Nitroxide mediated radical polymerizationDispersityRadical polymerizationFree radicals010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisStyreneStyrenesPolymerizationchemistry.chemical_compoundLiving free-radical polymerizationColloid and Surface ChemistryRadical polymerizationPolymer chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryAlkylchemistry.chemical_classification010405 organic chemistryGeneral Chemistry[CHIM.CATA]Chemical Sciences/CatalysisBond-dissociation energyBond cleavage0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryPolymerization
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Preparation of drug-polymer composites by polymerization in supercritical carbon dioxide: a new method to increase the dissolution rate of bioactive …

2008

Supercritical carbon dioxide drug delivery system solid dispersion dissolution free radical polymerizationSettore ING-IND/27 - Chimica Industriale E Tecnologica
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Preparation of pH sensitive poly(vinilydenefluoride) porous membranes by grafting of acrylic acid assisted by supercritical carbon dioxide

2012

Free radical grafting of acrylic acid (AA) on poly(vinilydenefluoride) (PVDF) porous membranes was studied at 65°C using supercritical carbon dioxide (scCO 2) as a solvent and delivery agent. The process was initiated by the thermal decomposition of benzoylperoxide (BPO). Spectroscopic analyses confirmed the presence of poly(AA) chains linked to treated membranes. The mass fraction of grafted AA increased with grafting time and BPO concentration while it decreased when the density of the fluid phase was enhanced. A not-monotonic trend was obtained when the effect of the initial AA concentration was studied. The grafting process was accompanied by a reduction of the crystallinity of the PVDF…

PH-dependentGrafting proceGeneral Chemical EngineeringRadical polymerizationpH-sensitive polymersMass fractionPoly(vinylidene fluoride)Free radical graftingGrafting degreeCarboxylic acidRelease experimentAcrylic acidSupercritical fluid extraction Grafting (chemical)chemistry.chemical_compoundCrystallinityPVDF membraneFree radicalPolymer chemistrypH sensorPhysical and Theoretical ChemistryFluid-phasepH sensitiveAcrylic acidCrystallinitieDecompositionSupercritical carbon dioxideFree radical polymerizationChemistrySupercritical carbon dioxides Carbon dioxideSettore ING-IND/27 - Chimica Industriale E TecnologicaCondensed Matter PhysicsGraftingSolventMembraneSpectroscopic analysiPorous membraneNuclear chemistryThe Journal of Supercritical Fluids
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