Search results for "cyclophosphazenes"

showing 4 items of 4 documents

New phosphazene-based chain extenders containing allyl and epoxide groups

2003

In this paper we present the synthesis and the characterization of cyclophosphazenes substituted with allyl groups, their transformation in epoxide-containing cyclophosphazenes and the final utilization of these compounds as chain extenders in combination with polyamides. The reaction at high temperature of Nylon-6 with epoxy-functionalized cyclophosphazenes leads to the opening of the epoxy units by the action of both amino (--NH2) and carboxylic (--COOH) end-groups of the polymer to enhance the final molecular weight of this material. The consequences of this fact on the thermal, mechanical and visco-elastic properties of treated Nylon-6 have been also evaluated and compared to those of t…

Polymers and PlasticsGeneral Chemical EngineeringEpoxidechemistry.chemical_compoundPolymer chemistryMaterials ChemistryOrganic chemistryThermal stabilityPhosphazenechemistry.chemical_classificationchain extensionpolyamideGeneral ChemistryEpoxyPolymerNMREnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon 6chemistryvisual_artPolyamidecyclophosphazeneNylon-6; cyclophosphazenes; chain extension; polyamides; NMR.visual_art.visual_art_mediumnylon-6Designed Monomers and Polymers
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Reactions Occurring during the Melt Mixing of Nylon 6 and Oxazoline−Cyclophosphazene Units

2009

Specific reactions of amino and carboxyl end groups of Nylon 6 with the reactive oxazoline groups belonging to a cyclophosphazene compound (referred as CP20XA) were carried out at 240 °C for different times, under inert atmosphere. Ny6 polymers terminated with one specific reactive chain end (-COOH or NH2) were reacted with different amounts of CP20XA to study the kinetic order of the reactions. All Ny6-CP20XA reacted products soluble in trifluoroethanol (TFE) were well characterized by MALDI-TOF MS, FT-IR and ( 1H and 13C) NMR techniques. The MALDI-TOF results show that the oxazoline rings react with the carboxyl chain ends of Ny6 following second-order kinetics. The reactions with amino c…

chemistry.chemical_classificationOxazolineReaction mechanismPolymers and PlasticsOrganic ChemistryKineticsSide reactionPolymerOxazolineReactive BlendingInorganic Chemistrychemistry.chemical_compoundEnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon6Nylon 6chemistrycyclophosphazenes polyamide end-functionalization MALDI-TOFMaterials ChemistryOrganic chemistryInert gasMALDIMacromolecules
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Chemical Reactions occurring in the molten state between Ny6 and Oxazoline groups linked to a Cyclophosphazene moiety

2009

Settore ING-IND/22 - Scienza E Tecnologia Dei Materialicyclophosphazenes polyamide end-functionalization MALDI-TOF
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Cyclo- and Polyphosphazenes for Biomedical Applications

2022

Cyclic and polyphosphazenes are extremely interesting and versatile substrates characterized by the presence of -P=N- repeating units. The chlorine atoms on the P atoms in the starting materials can be easily substituted with a variety of organic substituents, thus giving rise to a huge number of new materials for industrial applications. Their properties can be designed considering the number of repetitive units and the nature of the substituent groups, opening up to a number of peculiar properties, including the ability to give rise to supramolecular arrangements. We focused our attention on the extensive scientific literature concerning their biomedical applications: as antimicrobial age…

polyphosphazenesOrganic ChemistryPharmaceutical SciencepolyphosphazeneAnalytical Chemistrycyclophosphazenes; drug delivery; polyphosphazenes; tissue engineeringChemistry (miscellaneous)Settore CHIM/03 - Chimica Generale E Inorganicatissue engineeringDrug Discoverydrug deliverycyclophosphazenescyclophosphazeneMolecular MedicinePhysical and Theoretical Chemistry
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