Search results for "ring-opening polymerization"

showing 10 items of 85 documents

Phosphasalen group IV metal complexes: synthesis, characterization and ring opening polymerization of lactide.

2020

International audience; We report the synthesis of a series of Zr and Ti complexes bearing phosphasalen which differs from salen by the incorporation of two P atoms in the ligand backbone. The reaction of phosphasalen proligands (1a-1c)H2 with Zr(CH2Ph)4 led to different products depending on the nature of the N,N-linker in the ligand. In case of ethylene-linked phosphasalen, octahedral Zr complex 2a formed as a single stereoisomer in trans geometry. With the phenylene linker, it was shown by dynamic NMR spectroscopy that complex 2b exists as a mixture of trans and cis-β isomers in solution, both enantiomers (Δ and Λ) of the cis-β isomer being in fast equilibrium with respect to the NMR tim…

010402 general chemistryLIGANDS SYNTHESIS01 natural sciencesRing-opening polymerizationCoordination complexInorganic ChemistryINDIUM COMPLEXESOctahedral molecular geometry[CHIM]Chemical SciencesSALALEN COMPLEXESCYCLIC ESTERSCOORDINATION CHEMISTRYZIRCONIUM COMPLEXES; COORDINATION CHEMISTRY; SALALEN COMPLEXES; LIGANDS SYNTHESIS; INDIUM COMPLEXES; SALEN LIGANDS; CYCLIC ESTERS; INITIATORS; CATALYSIS; ALUMINUMchemistry.chemical_classification010405 organic chemistryLigandCATALYSISCationic polymerizationNuclear magnetic resonance spectroscopyALUMINUM0104 chemical sciencesCrystallographychemistrySALEN LIGANDSAlkoxy groupINITIATORS[CHIM.OTHE]Chemical Sciences/OtherIsomerizationZIRCONIUM COMPLEXESDalton transactions (Cambridge, England : 2003)
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Ring opening polymerization of d,l-lactide and ε-caprolactone catalysed by (pyrazol-1-yl)copper(ii) carboxylate complexes

2021

1,2-Bis{(3,5-dimethylpyrazol-1-yl)methyl}benzene (L) reacts with [Cu(OAc)2] and C6H5COOH, 4-OH-C6H4COOH, 2-Cl-C6H4COOH and (3,5-NO2)2-C6H3COOH to afford the copper complexes [Cu2(C6H5COO)4(L)2] (1), [Cu2(4-OH-C6H4COO)4(L)2] (2), [Cu2(2-Cl-C6H4COO)4(L)2]n (3) and [Cu{(3,5-NO2)2-C6H3COO}2L]n (4) which are characterised by IR, mass spectrometry, elemental analyses, and X-ray crystallography. The structural data revealed two geometries that are adopted by the complexes: (i) paddle wheel in 1, 2·7H2O, 3 and (ii) regular chains in 3 and 4. Magnetic studies show strong antiferromagnetic couplings in the paddle wheel complexes and a weak antiferromagnetic coupling in the monometallic chain one. Cat…

010405 organic chemistryChemistryGeneral Chemical EngineeringDispersityGeneral Chemistry010402 general chemistry01 natural sciencesRing-opening polymerization0104 chemical scienceschemistry.chemical_compoundEnd-groupPaddle wheelPolymerizationPolycaprolactonePolymer chemistryCarboxylateCaprolactoneRSC Advances
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The complementary structural studies of the double metal cyanide type catalysts for the ring opening polymerization of the oxiranes

2016

010407 polymersPolymers and PlasticsChemistryGeneral Chemical EngineeringCyanideInorganic chemistryDouble metal010402 general chemistry01 natural sciencesRing-opening polymerization0104 chemical sciencesCatalysischemistry.chemical_compoundMaterials ChemistryThermal analysisPolimery
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Some New Copolymers by Ionic Polymerization

1980

In the first part the cationic polymerization of a homologous series of cyclic ether–acetals with ring sizes of 11, 14, and 17 atoms is described. During the polymerization of triethylene glycol formal (TGF) an equilibrium is reached and besides high polymers cyclic oligomers are formed. The oligomers and the polymers are built up of a regular sequence of one oxymethylene unit and three oxyethylene units –[–(OCH2) (OC2H4)3–]–x. They are therefore be labelled a “sequenced copolymer.” The equilibrium concentrations of the cyclic oligomers with a polymerization degree from 2 to 15 follow the Jacobson–Stockmayer equation. The 14- and 17-membered monomers POC and HOC forms cyclic oligomers and h…

Anionic addition polymerizationChain-growth polymerizationPolymers and PlasticsPolymerizationChemistryPolymer chemistryMaterials ChemistryCationic polymerizationCopolymerLiving polymerizationIonic polymerizationRing-opening polymerizationPolymer Journal
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On thermal behaviour of DMC catalysts for ring opening polymerization of epoxides

2016

Abstract The thermoanalytical studies of two types of the double metal cyanide catalysts were carried out. The identity of the catalysts was characterized by an elemental analysis and FTIR. The thermoanalytical examinations performed with the use of TG-DSC, EGA-FTIR, EGA-MS shed new light on views of the bonding of the ligands in the DMC. The chemical justification of the processes responsible for the TG/DSC steps was proposed. Several organic ligand complexing states were found in both types of catalysts. The ligand-DMC bondings were decomposing stepwise in relatively low temperature ranges, which could suggest their negligible role at catalytic reaction being performed usually at higher t…

Base (chemistry)CyanideInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesRing-opening polymerizationCatalysisDSCchemistry.chemical_compoundEGAPhysical and Theoretical ChemistryThermal analysisInstrumentationchemistry.chemical_classificationLiganddouble metal cyanide021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical scienceschemistryTGDMC catalysts0210 nano-technologyCobaltStoichiometrythermal analysisThermochimica Acta
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Transition Metal Catalyzed Olefin, Cycloolefin, and Styrene Polymerization

2013

The sections in this article are History and Trends Polymerization Processes Supported Catalysts and Morphology Control Polymerization Mechanisms and Stereoselectivity History and Principles of Metallocene Catalysis Regio- and Stereoselective Polymerization of α-Olefins Polymerization of Cyclic Olefins, Cyclopolymerization, and Stereoselective Polymerization of Styrene Late Transition Metal Catalysts Transition Metal Catalyzed Copolymerization Acknowledgements

Chain-growth polymerizationMaterials sciencePolymerizationPolymer chemistryCationic polymerizationLiving polymerizationOrganic chemistryCoordination polymerizationChain transferIonic polymerizationRing-opening polymerization
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Long-Chain Branched Poly(Lactide)s Based on Polycondensation of AB2 -type Macromonomers

2012

A series of long-chain branched poly(d-/l-lactide)s is synthesized in a two-step protocol by (1) ring-opening polymerization of lactide and (2) subsequent condensation of the preformed AB2 macromonomers promoted by different coupling reagents. The linear AB2 macromonomers are prepared by Sn(Oct)2-catalyzed ROP of D- and L-lactide with 2,2-bis(hydroxymethyl)butyric acid (BHB) as an initiator. Optimization of the polymerization conditions allows for the preparation of well-defined macromonomers (Mw/Mn = 1.09–1.30) with adjustable molecular weights (760–7200 g mol−1). The two-step approach of the synthesis comprises as well the coupling of these AB2 macromonomers and hence allows precise contr…

Condensation polymerLactidePolymers and PlasticsOrganic ChemistryCondensed Matter PhysicsBranching (polymer chemistry)Ring-opening polymerizationPolyesterchemistry.chemical_compoundchemistryPolymerizationReagentPolymer chemistryMaterials ChemistryHydroxymethylPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Aliphatic Hyperbranched Copolyesters by Combination of ROP and AB2-Polycondensation

2005

Hyperbranched aliphatic copolyesters have been prepared by the copolymerization of e-caprolactone and 2,2-bis(hydroxymethyl)butyric acid (AB 2 -monomer), catalyzed by (i) HfCl 4 (THF) 2 and (ii) diphenylammonium trifluoromethanesulfonate (DPAT), respectively. In both cases, copolymerization by combined ROP/AB 2 -Polycondensation was achieved. The degree of branching (DB) and consequently the density of functional groups of the resulting copolyesters were controlled by the comonomer ratio in the feed. Molecular weights in the range M n =22 000-166 000 g mot -1 (GPC, PS standards) were obtained, with apparent polydispersity indices of 1.20 to 1.95. The DB was in the range 0.03-0.35. Remarkabl…

Condensation polymerPolymers and PlasticsChemistryComonomerOrganic ChemistryCondensed Matter PhysicsBranching (polymer chemistry)Ring-opening polymerizationEnd-groupchemistry.chemical_compoundMonomerPolymer chemistryMaterials ChemistryHydroxymethylPhysical and Theoretical ChemistryTrifluoromethanesulfonateMacromolecular Chemistry and Physics
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Soluble Hyperbranched Poly(glycolide) Copolymers

2010

A series of (hyper)branched poly(glycolide) copolymers has been prepared by copolymerization of glycolide (GA) with 2,2-bis(hydroxymethyl)butyric acid (BHB) via combined ROP/AB2-polycondensation. Polymerization was conducted in bulk and catalyzed by stanneous-2-ethyl hexanoate (Sn(Oct)2). The branched topology of the resulting polyesters was studied in detail by 1D- and 2D-NMR spectroscopy and confirmed by the synthesis and characterization of model compounds. The AB2 monomer BHB was incorporated either as a dendritic or focal unit, but hardly in linear or terminal mode. As expected for multifunctional polycondensation, SEC measurements showed polydisperse products with polydispersity index…

Condensation polymerPolymers and PlasticsChemistryOrganic ChemistryDispersityCondensation reactionRing-opening polymerizationInorganic Chemistrychemistry.chemical_compoundMonomerPolymerizationPolymer chemistryMaterials ChemistryCopolymerHydroxymethylMacromolecules
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Hyperbranched Polylactide Copolymers

2006

A series of hyperbranched poly(l-lactide) (PLLA) copolymers were prepared by copolymerization of dilactide with 2,2-bis(hydroxymethyl)butyric acid (BHB) as an AB2 comonomer via a combined ring-open...

Condensation polymerPolymers and PlasticsComonomerOrganic ChemistryRing-opening polymerizationInorganic ChemistryButyric acidchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryMelting pointCopolymerMoleculeOrganic chemistryHydroxymethylMacromolecules
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