Search results for "Coordination polymerization"

showing 8 items of 18 documents

Infinite coordination polymer networks metallogelation of aminopyridine conjugates and in situ silver nanoparticle formation

2018

Herein we report silver(i) directed infinite coordination polymer network (ICPN) induced self-assembly of low molecular weight organic ligands leading to metallogelation. Structurally simple ligands are derived from 3-aminopyridine and 4-aminopyridine conjugates which are composed of either pyridine or 2,2'-bipyridine cores. The cation specific gelation was found to be independent of the counter anion, leading to highly entangled fibrillar networks facilitating the immobilization of solvent molecules. Rheological studies revealed that the elastic storage modulus (G') of a given gelator molecule is counter anion dependent. The metallogels derived from ligands containing a bipyridine core dis…

STABILIZATIONSilverCoordination polymerNanoparticleMetal Nanoparticles02 engineering and technologyorganometalliyhdisteet010402 general chemistry01 natural sciencesSilver nanoparticlePolymerizationchemistry.chemical_compoundBipyridinePyridineorganometallic compoundsMoleculePARTICLESCRYSTAL-STRUCTURES4-Aminopyridinepolymeeritta116GELSpolymersgeelitHYBRID MATERIALSta114General Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsGELATION0104 chemical sciencesCrystallographyREDUCTIONCross-Linking ReagentschemistryPolymerizationMETALLUMINESCENCEPHASE-TRANSITIONCoordination polymerizationnanohiukkasetnanoparticles0210 nano-technologyRheologySOFT MATTER
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Mechanistic study on the metallocene-based tandem catalytic coordinative chain transfer polymerization for the synthesis of highly branched polyolefi…

2021

Abstract Creation and control of long-chain branches (LCBs) in coordination polymerization of olefins is an enduring focus of research in both academia and industry. We have recently introduced a tandem catalytic coordinative chain transfer polymerization reaction where upon the concerted function of the polymerization catalyst, the chain transfer agent (CTA), and the displacement catalyst, a highly branched microstructure can be formed. Here we introduce a new tandem catalytic system using Et(Ind)2ZrCl2 as the polymerization catalyst. Despite the optimal reaction temperature for the cooperative function of catalyst components is lower than the ideal temperature for the productivity of the …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryGeneral Physics and AstronomyChain transfer02 engineering and technologyPolymerPost-metallocene catalyst010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundMonomerchemistryPolymerizationChemical engineeringMaterials ChemistryCoordination polymerization0210 nano-technologyMetalloceneEuropean Polymer Journal
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Effect of bulkiness and lewis acidity of aluminium compounds on the anionic polymerization of methyl methacrylate in toluene

1996

The bulkiness and the Lewis acidity of added aluminium compounds strongly affect the polymerization of methyl methacrylate in toluene at −78°C. The polymerization strongly deviates from ‘ideal’ first-order kinetics, i.e. the first-order time-conversion plots are kinked at low monomer conversions. Additionally, for the more bulky and more Lewis-acid aluminium alkyls, the time-conversion plots show a further downward curvature. This curvature is not the result of a termination reaction because the polymers are free of side products like β-ketoesters or vinyl ketone units. The molecular weight distributions and tacticities of the resulting polymers are also affected. Dependent on the aluminium…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic Chemistrychemistry.chemical_elementPolymerCondensed Matter Physicschemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationAluminiumTacticityPolymer chemistryMaterials ChemistryCoordination polymerizationMethyl methacrylateMacromolecular Symposia
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MCM-41 and related materials as media for controlled polymerization processes

1994

The synthesis of mesoporous MCM-41 type materials based on transition metal oxides and the polymerization of several monomers within MCM-41 is presented with the aim to specifically investigate the effects of the interface and confinement on host-guest interactions. In addition to standard MCM-41, material based on transition metal oxides is obtained although template removal has been unsuccessful for such compounds until now. In situ polymerization of styrene, methyl methacrylate and vinyl acetate is possible within the mesopore system. The properties of some of the encapsulated polymers differ markedly with those obtained in the bulk.

chemistry.chemical_classificationMaterials sciencemacromolecular substancesPolymerchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryVinyl acetateCoordination polymerizationIn situ polymerizationMethyl methacrylateIonic polymerizationMesoporous material
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Katalizatory i proces koordynacyjnej polimeryzacji etylenu - eksperyment i teoria

2004

Badania eksperymentalne i teoretyczne koordynacyjnej polimeryzacji etylenu przeprowadzono wobec katalizatorów otrzymanych z prekursorów - kompleksów halogenków Ti, Zr, Hf, V z organicznymi zasadami Lewisa, nośnika magnezowego [MgCl2(THF)2] i związków glinoorganicznych. Określono zależnosć pomiędzy rodzajem halogenków w prekursorze a aktywnością katalizatora wanadowego. Ustalono profile energetyczne reakcji insercji i terminacji (beta-eliminacji) oraz przeniesienia atomu wodoru beta. Obliczone wartości barier insercji, a także energii wiązania etylenu do centrum aktywnego dobrze korelują z wynikami polimeryzacji. Stwierdzono występowanie w centrach aktywnych oddziaływań agostycznych, które o…

energetic profilesHfkompleksy halogenków TiZrHf i Vreakcja terminacjikoordynacyjna polimeryzacja etylenuprofil energetycznycatalytic activitynośnik magnezowyreakcja insercjimagnesium supportV halidesdensity functionals method (DFT)aktywność katalitycznaoxygen-donor ligandsinsertion and termination reactionspolimeryzacja etylenucoordination polymerization of ethylenecomplexes of Tiligandy tlen-donorowePolimery
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Vanadium-based Ziegler-Natta catalyst supported on MgCl2(THF)2 for ethylene polymerization

1996

A supported magnesium‐vanadium‐aluminium catalyst was prepared by depositing –with the use of a milling technique–VOCl3 on the MgCl2(THF)2 support and subsequent activation with diethylaluminium chloride. Catalytic activity of the obtained system for ethylene polymerization was evaluated as a function of Mg/V and Al/V ratios as well as catalyst ageing time and polymerization temperature. High concentrations of THF in the catalytic system and considerable excess of an organoaluminium co‐catalyst were found to have no deactivating action on vanadium active sites. The catalyst obtained is stable and its activity for ethylene polymerization is high. It yields polyethylene with higher molecular …

inorganic chemicalsDiethylaluminium chloridePolymers and PlasticsOrganic Chemistrytechnology industry and agricultureVanadiumchemistry.chemical_elementSolution polymerizationPolyethyleneCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCoordination polymerizationZiegler–Natta catalystMacromolecular Rapid Communications
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Metallocenes and post-metallocenes immobilized on ionic liquid-modified silica as catalysts for polymerization of ethylene

2014

Abstract The supported ionic liquid (SIL) strategy was used for the first time to metallocene and post-metallocene heterogeneous catalysts for olefin polymerization. The metal complexes: Cp2TiCl2, Cp2ZrCl2, FI–Ti, and Sal–Ti were immobilized in the 1-(3-triethoxysilyl)propyl-3-methylimidazolium alkylchloroaluminate ionic liquid, anchored on the surface of the mesoporous amorphous silica. The SIL systems were characterized by FTIR, 29Si NMR, N2 adsorption, EA, AAS, TG, and SEM techniques. The developed supported catalytic systems were found to be active in the ethylene polymerization and produce the polyethylene of various properties.

polyethyleneChemistryProcess Chemistry and TechnologyPost-metallocene catalystPolyethyleneCatalysischemistry.chemical_compoundAdsorptionPolymerizationsilicaIonic liquidPolymer chemistryorganometallic catalystCoordination polymerizationMesoporous materialMetalloceneionic liquidApplied Catalysis A : General : an International Journal Devoted to Catalytic Science and its Applications
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A supported titanium postmetallocene catalyst: Effect of selected conditions on ethylene polymerization

2011

Ethylene polymerization with a titanium complex [N,N-ethylenebis(3-methoxysalicylideneiminato)titanium dichloride] immobilized on the magnesium support with the formula MgCl2(THF)0.32(Et2AlCl)0.36 was studied. In particular, the effects of polymerization temperature, monomer pressure, and polymerization time on the activity of the catalyst and on the polyethylene properties (molecular weight and its distribution, melting point, crystallinity, and bulk density) were evaluated. The findings of investigations prove that the studied supported titanium catalyst is highly active in ethylene polymerization, and its activity increases with increasing temperature and monomer pressure. Moreover, stab…

polyethyleneMaterials sciencePolymers and PlasticsBulk polymerizationsupportsmelting pointtechnology industry and agriculturechemistry.chemical_elementSolution polymerizationGeneral Chemistrymolecular weight distributionPolyethylenecatalystsSurfaces Coatings and Filmschemistry.chemical_compoundChain-growth polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryPrecipitation polymerizationCoordination polymerizationTitaniumJournal of Applied Polymer Science
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