Search results for "Glycidol"

showing 6 items of 36 documents

Double-Hydrophilic Linear-Hyperbranched Block Copolymers Based on Poly(ethylene oxide) and Poly(glycerol)

2008

A convenient 4-step (2-pot) approach for the synthesis of biocompatible, double hydrophilic linear-hyperbranched block copolymers based on poly(ethylene oxide) (PEO) and poly(glycerol) (PG) is described. The polymers consisting exclusively of an aliphatic polyether structure were prepared from linear PEO-b-(l-PG) precursor block copolymers, obtained via anionic polymerization of ethylene oxide and subsequently ethoxyethyl glycidyl ether (EEGE). In order to generate initiating functionalities for glycidol, the protected hydroxyl groups of the P(EEGE) block were recovered by hydrolysis with hydrochloric acid. Partial deprotonation of the linear poly(glycerol) block with cesium hydroxide permi…

chemistry.chemical_classificationPolymers and PlasticsEthylene oxideOrganic ChemistryDispersityGlycidolPolymerInorganic Chemistrychemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryAlkoxidePolymer chemistryMaterials ChemistryCopolymerOrganic chemistryMacromolecules
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Hyperbranched Polyglycerols with Elevated Molecular Weights: A Facile Two-Step Synthesis Protocol Based on Polyglycerol Macroinitiators

2009

Hyperbranched polyglycerol (PG) is established as one of the few hyperbranched polymers that offer the possibility to control molecular weight up to Mn = 6000 g/mol. This work introduces a facile 2-step strategy that relies on the use of a low molecular weight PG (Mn = 500 and 1000 g/mol) as a macroinitiator for the slow addition of glycidol, permitting to overcome previous limitations concerning molecular weights and molecular weight control. A systematic investigation of the effect of the degree of deprotonation on the control of the polymerization reaction has been carried out. A series of hyperbranched PGs with molecular weights up to Mn = 24000 g/mol has been obtained under fully contr…

chemistry.chemical_classificationPolymers and PlasticsMolecular massOrganic ChemistryGlycidolEpoxidePolymerRing-opening polymerizationInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryMoleculeMacromolecules
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One-step synthesis of multi-alkyne functional hyperbranched polyglycerols by copolymerization of glycidyl propargyl ether and glycidol

2013

By copolymerization of glycidol with the alkyne-containing oxirane monomer glycidyl propargyl ether (GPE), hyperbranched polyglycerol (hbPG) with a defined number of alkyne functionalities (up to 38%) can be obtained in a one-step procedure. The number of alkynes can be adjusted by the glycidol/GPE ratio to provide multi-alkyne functional hbPGs, maintaining the highly branched polyether structure. Interestingly, the acidic proton of the alkyne moiety does not interfere with the proton exchange mechanism during the polymerization of glycidol. By specific modification of the synthesis procedure, crosslinking reactions can be suppressed. The polymers exhibit molecular weights ranging from 1800…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryGlycidolAlkyneBioengineeringBranching (polymer chemistry)BiochemistryCycloadditionchemistry.chemical_compoundMonomerPolymerizationchemistryPolymer chemistryCopolymerAzidePolymer Chemistry
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Linear-Hyperbranched Graft-Copolymers via Grafting-to Strategy Based on Hyperbranched Dendron Analogues and Reactive Ester Polymers

2012

The synthesis of hyperbranched polyglycerol dendron analogues with precisely one focal amino functionality (H2N-hbPG) and their use for the synthesis of linear-hyperbranched graft-copolymers in a grafting-to approach is reported. By use of N,N-dibenzyl tris(hydroxylmethyl) aminomethane as a novel initiator for the ring-opening multibranching polymerization of glycidol, dendron analogues with one focal amino functionality of molecular weights ranging from 500 to 15000 g mol–1 and narrow to moderate polydispersities (Mw/Mn = 1.2–1.9) were synthesized, as confirmed by NMR and SEC. After removal of the benzyl protective groups, the accessibility and selective transformation of the focal amino g…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryGlycidolPolymerMethacrylateGraftingInorganic Chemistrychemistry.chemical_compoundchemistryPolymerizationDendrimerPolymer chemistryMaterials ChemistryCopolymerSide chainMacromolecules
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Systematic investigation of functional core variation within hyperbranched polyglycerols

2008

A novel series of hyperbranched polyether polyols with various n-alkyl amine cores (mono- and bifunctional) and photoactive cores (benzylamine and 1-naphthylmethylamine) have been prepared. Polymerization of glycidol was carried out in two ways, starting directly from primary amine initiators and from bisglycidolized amine initiators. NMR spectroscopy and size exclusion chromatography (SEC) showed good control over the molecular weights only, when bisglycidolized amines were used. Molecular weights and polydispersity of the hyperbranched polyglycerols prepared with these initiator-cores were in the range of 1600 to 8400 g/mol and of 1.5 to 2.5, respectively. MALDI-ToF mass spectrometry conf…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySize-exclusion chromatographyDispersityGlycidolPolymerRing-opening polymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryBifunctionalJournal of Polymer Science Part A: Polymer Chemistry
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ABA Triblock Copolymers Based on Linear Poly(oxymethylene) and Hyperbranched Poly(glycerol): Combining Polyacetals and Polyethers

2013

The synthesis of hyperbranched-linear-hyperbranched ABA triblock copolymers based on a linear poly(oxymethylene) (POM) block and hyperbranched poly(glycerol) (hbPG) blocks is described. The polymers containing a polyacetal polyether structure were prepared from linear bishydroxy-functional POM macroinitiators, obtained by cationic ring-opening polymerization of trioxane and 1,3-dioxolane as a comonomer with formic acid as a transfer agent and subsequent hydrolysis of the formate group. Partial deprotonation of the resulting hydroxyl groups permitted “hypergrafting” of glycidol by anionic ring-opening multibranching polymerization (ROMBP). With respect to the hyperbranched blocks, the obtain…

chemistry.chemical_classificationPolymers and PlasticsTrioxaneComonomerOrganic ChemistryCationic polymerizationGlycidolPolymerDegree of polymerizationInorganic Chemistrychemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryMacromolecules
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