Search results for "Macromolecular Substance"

showing 10 items of 882 documents

Reversible dehydration polymerization of terephthalate bridged [{Cu2(2,2′-bpy)2(tp)(H2O)3(NO3)}·H2O·NO3]2

2006

The title compound is the first example of a molecular magnet sponge, which exhibits a carboxylate-assisted unique reversible dehydrative polymerization–rehydrative monomerization phenomenon.

PolymerizationMolecular magnetsChemistryPolymer chemistrymedicinemacromolecular substancesGeneral ChemistryDehydrationequipment and suppliesmedicine.diseasehuman activitiesMendeleev Communications
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Crosslinked α,β-Polyasparthydrazide Micromatrices for Controlled Release of Anticancer Drugs

1995

The preparation of new hydrogels by the reaction of α,β- polyasparthydrazide and glutaraldehyde is reported. A different crosslinking degree was obtained by varying the ratio crosslinking agent/polymer which influenced the swelling behavior of the gel. 5-Fluorouracil, was incorporated into the matrices during the crosslinking reaction and in vitro release studies were performed in simulated gastric juice (pH 1.1) and pH 7.4 buffer solution. The hydrogels prepared were chemically stable in the dissolution media. The observed data show the potential application of these new matrices for peroral administration of anticancer agents.

Polymers and Plastics0206 medical engineeringBioengineeringmacromolecular substances02 engineering and technologyBiomaterialschemistry.chemical_compoundPolymer chemistryMaterials ChemistrymedicineDissolutionchemistry.chemical_classificationtechnology industry and agriculturePolymerBuffer solution021001 nanoscience & nanotechnology020601 biomedical engineeringControlled releaseIn vitrochemistrySelf-healing hydrogelsGlutaraldehydeSwellingmedicine.symptom0210 nano-technologyNuclear chemistryJournal of Bioactive and Compatible Polymers
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Diffusion of single molecular and macromolecular probes during the free radical bulk polymerization of MMA : towards a better understanding of the Tr…

2016

Free radical bulk polymerizations exhibit complex kinetics due to the viscosity increase during the polymerization process. Especially the termination rate constant can be strongly influenced by the mobility of polymer chains in the polymerization mixture. As a consequence an autoacceleration period, the so-called Trommsdorff effect, can be observed often. In order to investigate this behaviour on a nanoscopic scale, we directly visualized the mobility of molecules and macromolecules in polymerizing MMA solutions using a combination of highly sensitive fluorescence correlation spectroscopy and widefield fluorescence microscopy. For this purpose, rather monodisperse PMMA chains were synthesi…

Polymers and PlasticsBulk polymerizationDispersityBioengineeringFluorescence correlation spectroscopy02 engineering and technologymacromolecular substances010402 general chemistry01 natural sciencesBiochemistryAutoaccelerationPolymer chemistryReversible addition−fragmentation chain-transfer polymerizationchemistry.chemical_classificationOrganic Chemistrytechnology industry and agriculturePolymer021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringPolymerizationchemistryddc:540MMA; Trommsdorff effect0210 nano-technologyMacromolecule
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Group transfer and anionic polymerization: A critical comparison

1990

The mechanism of group transfer polymerization (GTP) of methacrylates in THF is investigated by using data on kinetics of homo- and copolymerization, polymer microstructure and molecular weight distribution. By comparison with corresponding data on anionic polymerization it is concluded that the mechanisms of monomer addition to the active chain end is very similar for both anionic and group transfer polymerization and that GTP is ionic in character. On the other hand, GTP uniquely is characterized by the existence of a catalyst exchange equilibrium. The position of this equilibrium determines the rates of polymerization, and the dynamics determine the molecular weight distribution.

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationtechnology industry and agricultureCationic polymerizationChain transfermacromolecular substancesCondensed Matter PhysicsChain-growth polymerizationAnionic addition polymerizationPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationIonic polymerizationMakromolekulare Chemie. Macromolecular Symposia
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Preparation of Hyperbranched Polyacrylates by Atom Transfer Radical Polymerization. 2. Kinetics and Mechanism of Chain Growth for the Self-Condensing…

1997

The self-condensing vinyl polymerization (SCVP) of 2-((2-bromopropionyl)oxy)ethyl acrylate (BPEA) has resulted in the formation of hyperbranched polyacrylates. The polymerization mechanism used to polymerize the BPEA was atom transfer radical polymerization (ATRP), a “living”/controlled radical polymerization. This paper details the study of the kinetics of polymerization and the growth of the macromolecule during the polymerization. The results obtained in the polymerization were compared to the theoretical predictions for SCVP. It was determined that the polymerization deviated from the ideal case, as a consequence of the establishment of a dynamic equilibrium in ATRP resulting in the add…

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationtechnology industry and agricultureCationic polymerizationChain transfermacromolecular substancesPhotochemistryInorganic ChemistryLiving free-radical polymerizationChain-growth polymerizationPolymerizationPolymer chemistryMaterials ChemistryReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationMacromolecules
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Synthesis and characterization of optically active 2,4-disubstituted-2-oxazolines and their polymerization

1994

Four different optically active 2,4-disubstituted-2-oxazolines were synthesized and characterized. Cationic polymerization of these oxazolines were studied. Three of the oxazolines could be polymerized using methyl trifluoromethanesulfonate as initiator. S-(–)-2-Phenyl-4-isopropyl-2-oxazoline could not be polymerized under the conditions used.

Polymers and PlasticsChemistryOrganic Chemistrytechnology industry and agricultureCationic polymerizationmacromolecular substancesOptically activeRing-opening polymerizationCharacterization (materials science)chemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryMethyl trifluoromethanesulfonatePolymer International
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Polyaspartamide based hydrogel with cell recruitment properties for the local administration of hydrophobic anticancer drugs

2019

Abstract By exploiting the chemical versatility and the high water dispersibility of α,β-poly(N-2-hydroxyethyl)D,L-aspartamide, in this work, two different polymer derivatives were synthesized for the first time. Obtained macromolecules were characterized and used to produce hydrogels exploitable for the local release of hydrophobic anticancer drugs. The first derivative, bearing pendant β-cyclodextrins, was employed to solubilize tamoxifen, chosen as a model drug, and to produce a water soluble supramolecular complex, as evidenced through tamoxifen phase solubility studies. The second derivative, bearing pendant Cyclo(Arginine-Glyicine-Asparagine-D-Phenilyalanine-Cysteine) peptide moieties…

Polymers and PlasticsGeneral Chemical EngineeringSupramolecular chemistryPeptideRegional chemotherapymacromolecular substances02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryMaterials ChemistryEnvironmental ChemistrySolubilityCytotoxicityPolyaspartamide RGD Hydrogel Regional chemotherapy Cell recruitmentchemistry.chemical_classificationRGDtechnology industry and agricultureGeneral Chemistry021001 nanoscience & nanotechnologyCell recruitmentCombinatorial chemistryIn vitro0104 chemical sciencesPolyaspartamideHydrogelchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoCancer cellSelf-healing hydrogels0210 nano-technologyMacromoleculeReactive and Functional Polymers
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Poly(methyl ethylene phosphate) hydrogels

2020

Abstract A degradable and water-soluble polyphosphoester (PPE), namely poly(methyl ethylene phosphate)-dimethacrylate (PMEP-DMA), was synthesized and crosslinked by UV irradiation to prepare PPE-hydrogels. Hydrogels with 10 and 15 wt% of PMEP were prepared after UV-irradiation with an additional 0.2 wt% of photoinitiator. The colorless and transparent PPE hydrogels were studied for their swelling and water uptake. The rheological analysis demonstrated their viscoelastic behavior. The PPE hydrogels were compared to poly(ethylene glycol) (PEG) hydrogels prepared from PEG-macromonomers of similar degrees of polymerization. Hydrolysis experiments proved a successful disintegration of the PPE hy…

Polymers and PlasticsGeneral Physics and Astronomy02 engineering and technologymacromolecular substancesStealth effect010402 general chemistry01 natural sciencescomplex mixturesHydrolysischemistry.chemical_compoundPolyphosphoesterPEG ratioMaterials Chemistrymedicinechemistry.chemical_classificationPoly(ethylene glycol)Organic Chemistrytechnology industry and agriculturePhosphorusPolymer021001 nanoscience & nanotechnology0104 chemical sciencesHydrogelchemistryPolymerizationChemical engineeringSelf-healing hydrogelsSwellingmedicine.symptom0210 nano-technologyPhotoinitiatorEthylene glycolEuropean polymer journal
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Evaluation of Charge‐Regulated Supramolecular Copolymerization to Tune the Time Scale for Oxidative Disassembly of β‐Sheet Comonomers

2019

A multistimuli-responsive supramolecular copolymerization is reported. The copolymerization is driven by hydrogen bond encoded β-sheet-based charge co-assembly into 1D nanorods in water, using glutamic acid or lysine residues in either of the peptide comonomers. The incorporation of methionine as hydrophobic amino acid supports β-sheet formation, but oxidation of the thioether side-chain to a sulfoxide functional group destabilizes the β-sheet ordered domains and induces disassembly of the supramolecular polymers. Using H2 O2 as reactive oxygen species, the time scale and kinetics of the oxidative disassembly are probed. Compared to the charge neutral homopolymers, it is found that the oxid…

Polymers and PlasticsMacromolecular SubstancesPolymersSupramolecular chemistryBeta sheet02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundThioetherAmphiphilePolymer chemistryMaterials ChemistryCopolymerAmino Acidschemistry.chemical_classificationNanotubesHydrogen bondOrganic ChemistryHydrogen BondingSulfoxideHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesSupramolecular polymerschemistryProtein Conformation beta-StrandPeptidesReactive Oxygen Species0210 nano-technologyOxidation-ReductionMacromolecular Rapid Communications
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Synthesis of multiarm star poly(glycerol)-block-poly(2-hydroxyethyl methacrylate).

2006

Well-defined multiarm star block copolymers poly(glycerol)-b-poly(2-hydroxyethyl methacrylate) (PG-b-PHEMA) with an average of 56, 66, and 90 PHEMA arms, respectively, have been prepared by atom transfer radical polymerization (ATRP) of HEMA in methanol by a core-first strategy. The hyperbranched macroinitiators employed were prepared on the basis of well-defined hyperbranched polyglycerol by esterification with 2-bromoisobutyryl bromide. Polydispersites M(w)/M(n) of the new multiarm stars were in the range of 1.11-1.82. Unexpectedly, with the combination of CuCl/CuBr(2)/2,2'-bipyridyl as catalyst, the polymerization conversion can be driven to maximum values of 79%. The control of CuCl cat…

Polymers and PlasticsMolecular StructureAtom-transfer radical-polymerizationMacromolecular SubstancesPolymersDispersityBioengineeringSolution polymerizationBiocompatible MaterialsMethacrylateCatalysisCatalysisPolyethylene GlycolsBiomaterialschemistry.chemical_compoundKineticschemistryPolymerizationModels ChemicalBromidePolymer chemistryMaterials ChemistryCopolymerMethacrylatesBiomacromolecules
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