Search results for " modifica"

showing 10 items of 817 documents

Synthesis of aldonamide siloxanes by hydrosilylation

1998

Abstract The synthesis of hydrophobic/hydrophilic hybrid polymers based on polydimethylsiloxanes (PDMS) and carbohydrate derivatives involving a hydrosilylation step is reported. Starting with poly(dimethyl- co -hydromethyl)siloxanes (PDMS- co -HMS), O -acetylated N -allylaldonamides of various sugars can be attached to the siloxane backbone using platinum catalysts. The characteristics of different transition metal complexes in the polymer-analogous formation of SiC bonds are investigated. A generalized reaction pathway applicable to several reducing carbohydrates is established to synthesize aldonamide siloxanes in a broad variety of molecular weight and composition. The products obtaine…

chemistry.chemical_classificationPolymers and PlasticsHydrosilylationOrganic Chemistrychemistry.chemical_elementChemical modificationPolymerCatalysischemistry.chemical_compoundchemistryTransition metalSiloxaneAldonic acidPolymer chemistryMaterials ChemistryOrganic chemistryPlatinumPolymer
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Cationic copolymers of ?,?-poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA) and ?,?-polyasparthylhydrazide (PAHy): synthesis and characterization

2000

In the present study the derivatization of two water-soluble synthetic polymers, α,β-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA) and α,β-polyasparthylhydrazide (PAHy), with glycidyltrimethylammonium chloride (GTA) is described. This reaction permits the introduction of positive charges in the macromolecular chains of PHEA and PAHy in order to make easier the electrostatic interaction with DNA. Different parameters affect the reaction of derivatization, such as GTA concentration and reaction time. PHEA reacts partially and slowly with GTA; on the contrary the reaction of PAHy with GTA is more rapid and extensive. The derivatization of PHEA and PAHy with GTA is a convenient method to introdu…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryCationic polymerizationChemical modificationPolymerPolyelectrolytechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerSurface modificationDerivatizationMacromoleculePolymer International
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Multilayer build-up of a reactive polymer with α,ω-functionalized chromophores

1997

Alternating multilayers with up to ten layers have been prepared by sequential reaction of a reactive polymer (poly[(1-methylvinyl isocyanate)-alt-(maleic anhydride)]) with α,ω-functionalized chromophores. For this purpose new chromophores were synthesized varying the length of the hydrophobic spacer. The analysis of the multilayer build-up shows that physisorption is more important than chemisorption for fixation of new polymer layers. Thus, a multilayer build-up is only possible with the shorter, more hydrophilic chromophore and not with the long hydrophobic spacer.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryChemical modificationMaleic anhydridePolymerChromophoreCondensed Matter PhysicsIsocyanatechemistry.chemical_compoundchemistryPhysisorptionChemisorptionMonolayerPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Synthesis and polymerization of active ester monomers based on 4-vinylbenzoic acid

2007

Abstract Nine active ester monomers based on 4-vinylbenzoic acid have been synthesized. Under free radical polymerization conditions these monomers could successfully be polymerized yielding reactive polymers with molecular weights of around M n  = 20.000–50.000 g/mol and molecular weight distributions M w / M n of around or below 2 in good yields. Polymer analogous reactions with amines have been investigated by time-resolved FT-IR spectroscopy and it was found that especially poly(pentafluorophenyl 4-vinylbenzoate) featured a significant reactivity, such that polymer analogous reactions proceeded quantitatively with amines within less than 5 min at 0 °C.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationGeneral Physics and AstronomyChemical modificationPolymerRing-opening polymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryReactivity (chemistry)Functional polymersEuropean Polymer Journal
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Versatile ω-end group functionalization of RAFT polymers using functional methane thiosulfonates

2009

Five different polymers, poly[methyl methacrylate] (PMMA), poly[lauryl methacrylate] (PLMA), poly[diethylene glycol methacrylate] (PDEGMA), poly[N-iso-propylacrylamide] (PNIPA), and poly[styrene] (PS) prepared by the RAFT process and thus terminated with dithioesters were aminolyzed in the presence of S-3-butynyl methane thiosulfonate (MTS), which was synthesized in two steps. Analysis of the polymers by 2D NMR, UV–vis absorbance, and gel permeation chromatogra-phy revealed them to quantitatively carry acetylene end groups connected with disul-fide bridges, indicating that functional MTS reagents can be employed for end group functionalization of RAFT polymers. This versatile method is of ad…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRaftPolymerMethacrylateContact anglechemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistrySurface modificationAzideMethyl methacrylateJournal of Polymer Science Part A: Polymer Chemistry
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pH-sensitive hydrogel based on a novel photocross-linkable copolymer.

2004

A pH sensitive hydrogel has been prepared by a UV irradiation technique. Starting polymer was the PHM (poly hydroxyethylaspartamide methacrylated) obtained from polyaspartamide (PHEA) partially derivatized with methacrylic anhydride (MA). This new copolymer has been further derivatized with succinic anhydride (SA) to obtain PHM-SA that has been cross-linked by UV irradiation to form a pH sensitive hydrogel. The network, recovered after washing as a powder, has been been characterized by FT-IR spectrophotometry and particle size distribution analysis. Moreover, to have information about water affinity of the prepared sample, swelling measurements have been carried out in aqueous media mimick…

chemistry.chemical_classificationPolymers and PlasticspH sensitive hydrogels polyaspartamide drug releasePolymersSuccinic anhydrideMethacrylic anhydrideChemical modificationBioengineeringHydrogelsPolymerHydrogen-Ion ConcentrationBiomaterialschemistry.chemical_compoundCross-Linking ReagentschemistryDrug deliveryPolymer chemistryMaterials ChemistryCopolymerMicroparticleDrug carrierNuclear chemistryBiomacromolecules
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Gamma radiation induced maleation of polypropylene using supercritical CO 2 : preliminary results

2000

Abstract The charging of maleic anhydride (MA) and dicumyl peroxide (DCP) into polypropylene matrices has been carried out by CO2 in supercritical conditions. The grafting of MA into polymer chains was done through gamma irradiation in CO2 atmosphere (0.1 MPa, 25°C). The grafting was successful and the amount of grafted anhydride was dependent on the amount of MA and DCP charged into the polypropylene matrix. The presence of grafted succinic anhydride was shown by FT-IR spectroscopy and its amount was determined through a calibration curve derived from standard samples. The effect of swelling due to supercritical CO2, maleic anhydride grafting and gamma irradiation on the molecular structur…

chemistry.chemical_classificationPolypropylenePolymers and PlasticsChemistryOrganic ChemistrySuccinic anhydrideChemical modificationMaleic anhydridePolymerGraftingSupercritical fluidchemistry.chemical_compoundChemical engineeringPolymer chemistryMaterials ChemistrymedicineSwellingmedicine.symptomPolymer
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New insights into the water-solubilization of thiol-sensitive fluorogenic probes based on long-wavelength 7-hydroxycoumarin scaffolds

2014

Abstract The synthesis and photophysical properties of novel water-soluble phenol-based fluorophores derived from 3-benzothiazolyl-7-hydroxycoumarin and emitting in the range 485–631 nm are described. Further conversion into thiol-sensitive fluorogenic probes through the chemical modification of their hydroxyl group was next investigated. Depending on the type of thiol-reactive quenching moiety used (2,4-dinitrobenzenesulfonyl ester, 2,4-dinitrophenyl ether or benzoquinone-type Michael acceptors) and the water-solubilizing group(s) pre-introduced into the coumarin core, dramatic differences in the thiol-induced fluorescence activation of these pro-fluorophores under physiological conditions…

chemistry.chemical_classificationQuenching (fluorescence)[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringChemical modificationEther[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.THER]Chemical Sciences/Medicinal ChemistryPhotochemistryCoumarinFluorescence[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiolPhenolMoietyComputingMilieux_MISCELLANEOUS[CHIM.CHEM]Chemical Sciences/CheminformaticsDyes and Pigments
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Inorganic Polymers: Morphogenic Inorganic Biopolymers for Rapid Prototyping Chain

2013

In recent years, considerable progress has been achieved towards the development of customized scaffold materials, in particular for bone tissue engineering and repair, by the introduction of rapid prototyping or solid freeform fabrication techniques. These new fabrication techniques allow to overcome many problems associated with conventional bone implants, such as inadequate external morphology and internal architecture, porosity and interconnectivity, and low reproducibility. However, the applicability of these new techniques is still hampered by the fact that high processing temperature or a postsintering is often required to increase the mechanical stability of the generated scaffold, …

chemistry.chemical_classificationRapid prototypingScaffoldBiocompatibilityNanotechnologyPolymerBiologyInterconnectivityBone tissue engineeringlaw.inventionchemistrylawBioactive glassSurface modification
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Isoreticular two-dimensional magnetic coordination polymers prepared through pre-synthetic ligand functionalization

2018

Chemical functionalization is a powerful approach to tailor the physical and chemical properties of two-dimensional (2D) materials, increase their processability and stability, tune their functionalities and, even, create new 2D materials. This is typically achieved through post-synthetic functionalization by anchoring molecules on the surface of an exfoliated 2D crystal, but it inevitably alters the long-range structural order of the material. Here we present a pre-synthetic approach that allows the isolation of crystalline, robust and magnetic functionalized monolayers of coordination polymers. A series of five isostructural layered magnetic coordination polymers based on Fe(ii) centres a…

chemistry.chemical_classificationSolucions polimèriquesChemistryLigandMagnetismGeneral Chemical EngineeringNanotechnology02 engineering and technologyGeneral ChemistryPolymerCiència dels materials010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesExfoliation joint0104 chemical sciencesMonolayerSurface modificationMoleculeIsostructural0210 nano-technologyNature Chemistry
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