Search results for "Ring-opening metathesis polymerisation"

showing 10 items of 11 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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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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1993

Nonlinear opticalChemistryAmphiphilePolymer chemistryMonolayerNonlinear opticsRing-opening metathesis polymerisationReactivity (chemistry)ChromophoreRing-opening polymerizationDie Makromolekulare Chemie, Rapid Communications
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Poly(phosphonate)s via Olefin Metathesis: Adjusting Hydrophobicity and Morphology

2014

Olefin metathesis step-growth (acyclic diene metathesis (ADMET)) and chain-growth (ring-opening metathesis) polymerization was used to prepare linear poly(phosphonate)s with variable hydrophilicity. The first phosphonate monomer, i.e., di(undec-10-en-1-yl) methylphosphonate, for ADMET polymerization was developed, and potentially degradable and biocompatible, unsaturated poly(phosphonate)s were prepared with molecular weights up to 23 000 g mol–1 with molecular weight dispersities Đ < 2. These polymers were studied with respect to their interaction with a calcium phosphate bone substitute material from an aqueous nanoparticle dispersion that was prepared by a solvent evaporation miniemulsio…

Polymers and PlasticsChemistryOrganic ChemistryROMPMetathesisPhosphonateInorganic Chemistrychemistry.chemical_compoundMonomerPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryRing-opening metathesis polymerisationAcyclic diene metathesisMacromolecules
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Synthesis and characterization of amphiphilic comb-polymers via ring-opening metathesis polymerization of exo,exo-5,6-bis(alkoxymethyl)-7-oxabicyclo[…

1994

A number of exo,exo-5,6-bis(alkoxymethyl)-7-oxabicyclo[2.2.1]hept-2-enes (exo,exo-5,6-bis(alkoxymethyl)-7-oxanorbornenes) with long alkyl chains were prepared by reduction of the Diels-Alder adduct of furan and maleic anhydride, followed by alkylation with a series of different n-alkylbromides. These monomers were polymerized via ring-opening metathesis polymerization (ROMP) catalyzed by ruthenium trichloride in ethanolic solution. Contrary to a helical conformation as it was predicted by a previous molecular model study the poly(7-oxanorbornenes) adopt a coil conformation in solution. In bulk the materials show side chain crystallization.

Polymers and PlasticsMaleic anhydrideGeneral ChemistryROMPAlkylationCondensed Matter PhysicsMetathesisRing-opening polymerizationchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistrySide chainRing-opening metathesis polymerisationPolymer Bulletin
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A “click” approach to ROMP block copolymers

2008

Amphiphilic block copolymers can be conveniently prepared via convergent syntheses, allowing each individual polymer block to be prepared via the polymerization technique that gives the best architectural control. The convergent “click-chemistry” route presented here, gives access to amphiphilic diblock copolymers prepared from a ring opening metathesis polymer and polyethylene glycol. Because of the high functional group tolerance of ruthenium carbene initiators, highly functional ring opening metathesis polymerization (ROMP) polymer blocks can be prepared. The described synthetic route allows the conjugation of these polymer blocks with other end-functional polymers to give well-defined a…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryROMPPolymerMetathesisRing-opening polymerizationEnd-groupPolymerizationchemistryPolymer chemistryMaterials ChemistryCopolymerRing-opening metathesis polymerisationJournal of Polymer Science Part A: Polymer Chemistry
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Functional end groups for polymers prepared using ring-opening metathesis polymerization.

2011

The precise placement of functional groups on the chain-ends of macromolecules is a major focus of polymer research. Most common living polymerization techniques offer specific methods of end-functionalization governed by the active propagating species and the kinetics of the polymerization reaction. Ring-opening metathesis polymerization has established itself as one of the most functional-group-tolerant living polymerization techniques known, but this tolerance has limited the number of available functionalization reactions. Metathesis chemists have therefore been required to develop a variety of end-functionalizations, adapting each of them to the reactivity scheme of the particular cata…

chemistry.chemical_classificationMolybdenumPolymer scienceMolecular StructureMacromolecular SubstancesPolymersGeneral Chemical EngineeringGeneral ChemistryPolymerMetathesisCatalysisRutheniumchemistryPolymerizationOrganometallic CompoundsSurface modificationLiving polymerizationRing-opening metathesis polymerisationReactivity (chemistry)MacromoleculeNature chemistry
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Monofunctional metathesis polymers via sacrificial diblock copolymers.

2006

chemistry.chemical_classificationchemistryPolymer chemistryCopolymerOrganic chemistryRing-opening metathesis polymerisationGeneral ChemistryPolymerMetathesisRing-opening polymerizationCatalysisAcyclic diene metathesisAngewandte Chemie (International ed. in English)
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