Search results for "polymerisation"

showing 10 items of 23 documents

Synthesis and biological evaluation of new bicyclic fluorinated uracils through ring-closing metathesis.

2006

Two families of bicyclic fluorinated uracils have been prepared starting from a gem-difluorinated unsaturated nitrile, by means of a ring-closing metathesis reaction to form the new ring, which is fused at the C-5/C-6 or N-1/C-6 positions of the uracil moiety. The selective formation of olefin regioisomers in the metathesis process can be controlled according to the reaction conditions (catalyst, solvent, and temperature). The acaricidal activities of the resulting compounds have also been investigated.

Bicyclic moleculeNitrileMolecular StructureChemistryOrganic ChemistryGeneral MedicineFluorineRing (chemistry)MetathesisChemical synthesisCombinatorial chemistrychemistry.chemical_compoundRing-closing metathesisSalt metathesis reactionOrganic chemistryRing-opening metathesis polymerisationMoietyUracilAcyclic diene metathesisThe Journal of organic chemistry
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Olefin metathesis reactions with fluorinated substrates, catalysts, and solvents.

2014

CyclodextrinsOlefin metathesisHalogenationLactamsChemistryHomogeneous catalysisStereoisomerismGeneral ChemistryMetallacycleAlkenesCatalysisCatalysisCyclooctanesOrganic reactionMetalsSphingosineSolventsRing-opening metathesis polymerisationOrganic chemistryPeptidesChemical reviews
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DFT analysis of titanium complexes with oxygen-containing bidentate ligands

2003

Strength of the TiO co-ordinate bond in several titanium complexes with bidentate ligands has been investigated by means of DFT. Mutual interaction of particular donors and their influence on Lewis acidity of the central atom have also been studied. The energy of ligand binding ranges from −19 to −454 kJ/mol, depending on the kind of donors. Calculations confirm that a strong donor, alkoxide anion, co-ordinatively saturates the titanium and makes binding of new ligands less exoenergetic. On the contrary, two oxygen atoms of similar donor number do not have much influence on each other. Strength of the TiO bonds in titanium complexes with certain oxygen-containing bidentate ligands has bee…

DenticityLewis baseChemistryStereochemistryProcess Chemistry and TechnologyZiegler–Natta catalystBinding energychemistry.chemical_elementDFTCatalysisCatalysisCrystallographychemistry.chemical_compoundOlefin polymerisationAtomDonor numberAlkoxideLewis acids and basesPhysical and Theoretical ChemistryTitaniumJournal of Molecular Catalysis A-Chemical
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Designed biodegradable hydrogel structures prepared by stereolithography using poly(ethylene glycol)/poly(D,L-lactide)-based resins

2010

Designed three-dimensional biodegradable poly(ethylene glycol)/poly(D,L-lactide) hydrogel structures were prepared for the first time by stereolithography at high resolutions. A photo-polymerisable aqueous resin comprising PDLLA-PEG-PDLLA-based macromer, visible light photo-initiator, dye and inhibitor in DMSO/water was used to build the structures. Porous and non-porous hydrogels with well-defined architectures and good mechanical properties were prepared. Porous hydrogel structures with a gyroid pore network architecture showed narrow pore size distributions, excellent pore interconnectivity and good mechanical properties. The structures showed good cell seeding characteristics, and human…

IR-80283Materials scienceStereolithographyPolyestersPharmaceutical ScienceDesigned porous structuresSCAFFOLDSHydrogel Polyethylene Glycol Dimethacrylatelaw.inventionPolyethylene GlycolsMacromer photo-polymerisationCONSTRUCTSchemistry.chemical_compoundMETIS-272859lawPolymer chemistryGLYCOL)Cell Adhesionmacromer photopolymerisationHumansTissue engineeringPorosityStereolithographyAqueous solutiontechnology industry and agricultureMesenchymal Stem CellsMacromonomerResins SyntheticPhotopolymerBiodegradation EnvironmentalchemistryChemical engineeringBiodegradable hydrogelsSelf-healing hydrogelsCELLS090301 BiomaterialsEthylene glycolGyroid
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Ziegler–Natta catalysts based on vanadium halides: a DFT study

2003

Abstract Ziegler–Natta ethylene insertion into the carbon–metal bond for a number of fragments containing vanadium on different oxidation states as well as the halogen ligands has been studied by means of DFT. It is shown that the complexation and insertion energies are strongly influenced by the charge on the transition metal atom and, to some extent, by the electronegativity of the halogen atom. Complexation energy varies in the range −129 to −159 kJ/mol for charged species and −64 to −77 kJ/mol for neutral ones. Insertion energy follows a similar pattern and ranges from −28 to −62 and −82 to −100 kJ/mol, respectively. The calculated values are compared with the experimental results and d…

Inorganic chemistryHalideVanadiumchemistry.chemical_elementVanadiumGeneral ChemistryDFTCatalysisTransition stateCatalysisElectronegativityTransition metalchemistryolefin polymerisationHalogenPhysical chemistryZiegler–Natta catalystsZiegler–Natta catalystCatalysis Today
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New practical tungsten(VI) based catalyst systems for ring opening metathesis polymerisation

2002

Abstract Tungsten(VI) complexes of the type trans -[WCl 2 (diol)(OAr) 2 ] were studied as catalyst precursors for ROMP of norbornene and dicyclopentadiene. These compounds form active catalysts when treated by simple Grignard reagents, such as methyl magnesium iodide or neophyl magnesium chloride. Moreover, polymerisations can be run under ambient atmosphere without complicated inert atmosphere techniques.

MagnesiumDiolchemistry.chemical_elementROMPMagnesium iodideCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryDicyclopentadieneMaterials ChemistryOrganic chemistryRing-opening metathesis polymerisationPhysical and Theoretical ChemistryNorborneneInorganic Chemistry Communications
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End Capping Ring-Opening Olefin Metathesis Polymerization Polymers with Vinyl Lactones

2008

The selective placement of a functional group at the chain end of a ring-opening metathesis polymer using ruthenium carbene initiators has been a significant limitation. Here we demonstrate a highly effective and facile end-capping technique for ROMP with living ruthenium carbene chain ends using single-turnover olefin metathesis substrates. Vinylene carbonate and 3H-furanone are introduced as functionalization and termination agents for the ruthenium-initiated ring-opening metathesis polymerization. This leads directly to the formation of functional polymer end groups without further chemical transformation steps. Aldehyde and carboxylic acid end groups can be introduced by this new method…

Magnetic Resonance SpectroscopyTime FactorsPolymerschemistry.chemical_elementDioxolesAlkenesMetathesisBiochemistryRutheniumCatalysisLactoneschemistry.chemical_compoundColloid and Surface ChemistryPolymer chemistryOrganometallic CompoundsRing-opening metathesis polymerisationMolecular StructureTransition metal carbene complexStereoisomerismGeneral ChemistryROMPReference StandardsRutheniumPolymerizationchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationMethaneCarbeneAcyclic diene metathesisJournal of the American Chemical Society
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Modelling polycarbonate synthesis rates on the example of bulk heteropolyaddition of diphenyl carbonate and bisphenol A diglycidyl ether

2016

This paper investigates the effects of increased reaction mixture viscosity on the kinetics of linear polymer creation in a bulk polyaddition process of diphenyl carbonate and bisphenol A diglycidyl ether. The paper presents a method for solving a system of bulk polyaddition of diphenyl carbonate and bisphenol A diglycidyl ether process balance equations, allowing the determinatiof the process kinetic parameters. Determination of polymerisation reaction kinetic parameters was also made possible by the use of the so-called partial reaction rate constant. Such an approach enabled a significant simplification of the mathematical expressions describing the heteropolyaddition process and provide…

Materials sciencePolymers and PlasticsKineticsreaction rate constantKinetics of polymerisations02 engineering and technology010402 general chemistry01 natural sciencesViscositychemistry.chemical_compoundReaction rate constantmodelling of polymerizationsMaterials ChemistryOrganic chemistryPolycarbonateBisphenol A diglycidyl etherMolar massheteropolyadditionGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicslinear polymer0104 chemical sciencesChemical engineeringPolymerizationDiphenyl carbonatechemistryvisual_artviscosityvisual_art.visual_art_medium0210 nano-technologyPolymer Bulletin
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Effect of preparation method on the properties of poly(methyl methacrylate)/mesoporous silica composites

2019

The preparation method of a polymer composite and the filler loading are amongst the factors that influence the properties of the final composites. This article studies the effect of these factors on the thermal stability and thermal degradation kinetics of poly(methyl methacrylate) (PMMA)/mesoporous silica (MCM-41) composites filled with small amounts of MCM-41. The PMMA/MCM-41 composites were prepared through in situ polymerisation and melt mixing methods, with MCM-41 loadings of 0.1, 0.3, and 0.5 wt.%. The presence of MCM-41 increased the thermal stability of PMMA/MCM-41 composites prepared by melt mixing, but in the case of the in situ polymerised samples, the MCM-41 accelerated the deg…

Mesoporous silica (MCM-41)Thermal degradation kineticThermal degradation kineticsMelt mixingIn situ polymerisationFOS: Environmental engineeringPoly(methyl methacrylate) (PMMA)Environmental engineeringSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie13C {1H} CP-MAS-NMRSettore CHIM/02 - Chimica Fisica
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1993

Nonlinear opticalChemistryAmphiphilePolymer chemistryMonolayerNonlinear opticsRing-opening metathesis polymerisationReactivity (chemistry)ChromophoreRing-opening polymerizationDie Makromolekulare Chemie, Rapid Communications
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