Search results for "Epichlorohydrin"

showing 5 items of 5 documents

N,N-Diallylglycidylamine: A Key Monomer for Amino-Functional Poly(ethylene glycol) Architectures

2012

The first application of N,N-diallylglycidylamine (DAGA) as a monomer for anionic ring-opening polymerization is presented. The monomer is obtained in a one-step procedure using epichlorohydrin and N,N-diallylamine. Both random and block copolymers consisting of poly(ethylene glycol) and poly(N,N-diallylglycidylamine) with adjusted DAGA ratios from 2.5 to 24% have been prepared, yielding well-defined materials with low polydispersities (Mw/Mn) in the range 1.04–1.19. Molecular weights ranged between 2600 and 10 300 g mol–1. Isomerization of allylamine to enamine structures during polymerization depending on time, temperature, and counterion has been realized. The kinetics of the formation o…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryTriad (anatomy)Inorganic Chemistrychemistry.chemical_compoundMonomermedicine.anatomical_structurechemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymermedicineProton NMREpichlorohydrinCounterionEthylene glycolMacromolecules
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Synthesis of oxazolidinones from N-aryl-carbamate and epichlorohydrin under mild conditions

2022

The reaction conditions for an enantiospecific synthesis of various N-aryl-oxazolidinones from N-aryl-carbamates and (R) or (S) epichlorohydrin were optimized. The N-aryl-oxazolidinones were applied to the synthesis of compounds of biological interest such as DuP 721, toloxatone and a linezolid analogue.

toloxatoneOrganic ChemistrycarbamateepichlorohydrinlinezolidSettore CHIM/06 - Chimica OrganicaOxazolidinoneArkivoc
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Water-insoluble β-cyclodextrin–epichlorohydrin polymers for removal of pollutants from aqueous solutions by sorption processes using batch studies: A…

2017

This review is dedicated to Giangiacomo Torri (Istituto di Chimica e Biochimica G. Ronzoni, Milan, Italy) in celebration of his retirement.; International audience; Although water-insoluble cyclodextrin-epichlorohydrin polymers have been known for half a century, these materials are of continued interest to the scientific community, in particular for their interesting environmental applications as sorbents in liquid-solid sorption processes. However, in spite of the abundance of literature and conclusive results obtained at the laboratory scale, interpreting the mechanisms of pollutant elimination remains an interesting source of debate and sometimes of contradiction. This review summarizes…

PollutantsPolymers and Plastics02 engineering and technologyWater insolubleLaboratory scale010402 general chemistry01 natural scienceschemistry.chemical_compoundMechanismsMaterials ChemistryCyclodextrinOrganic chemistryEpichlorohydrinPolymerComputingMilieux_MISCELLANEOUSPollutantchemistry.chemical_classificationAqueous solutionCyclodextrinOrganic ChemistrySorptionSurfaces and InterfacesPolymer021001 nanoscience & nanotechnology0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/PolymerschemistryChemical engineeringCeramics and CompositesEpichlorohydrin0210 nano-technologyCross-linking
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Anorganische verbindungen als lösungsmittel für polymere und monomere. Polymerisationen in phosphoroxychlorid und thionylchlorid

1966

Die Loslichkeit verschiedener Monomerer, Polymerer und Polymerisationskatalasatoren in anorganischen Verbindungen wurde untersucht. Chloride und Oxychloride des Phosphors und Schwefels zeigten gute Losungseigenschaften. Thionylchlorid und Phosphoroxychlorid wurden als Losungsmittel bei der kationischen Polymerisation von Styrol, Isobutylvinylather, 3,3-Bis-(chlormethyl)-oxetan, Tetrahydrofuran und Epichlorhydrin eingeaetzt. Als geeignete Katalysatoren erwiesen sich hierbei Aluminiumchlorid und Eisentrichlorid. In Phosphoroxychlorid konnten Acrylnitril und Vinylchlorid radikalisch polymerisiert werden. The solubility of a series of monomers, polymers, and initiators in inorganic compounds wa…

chemistry.chemical_compoundMonomerchemistryPolymer chemistrymedicineCationic polymerizationEpichlorohydrinAcrylonitrileVinyl etherChlorideTetrahydrofuranVinyl chloridemedicine.drugDie Makromolekulare Chemie
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Miscibility of Blends of Biodegradable Polymers and Copolymers with Different Plasticizers

2008

Miscibility between components of different plasticizer(A)/solvent(B)/biodegradable polymer(C) ternary systems with H-bonding has been compared. Systems were formed by two H-donor phenolic plasticizers, 4-nonylphenol (NP) and 4:4'-dihydroxydiphenylmethane (BPF); an H-acceptor solvent, epichlorohydrin (ECH); and H-acceptor poly(3-hydroxybutyrate) (PHB) or poly[(3-hydroxybutyrate)-co-(3-hydroxyvalerate)] (PHBHV) copolymers. Blend miscibility is the result of the balance of three competitive H-bondings: plasticizer self-association (AA), plasticizer-solvent (AB) and plasticizer-polymer (AC) interassociations. The strength and extent of such specific interactions have been experimentally monito…

Materials scienceTernary numeral systemPolymers and PlasticsOrganic ChemistryPlasticizerCondensed Matter PhysicsMiscibilityBiodegradable polymerSolventchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerEpichlorohydrinPhysical and Theoretical ChemistryTernary operationMacromolecular Chemistry and Physics
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