Search results for "RIZ"

showing 10 items of 9613 documents

Measurements on the temperature dependence of the cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst

1979

The cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst and at low monomer concentrations shows, at −15°C, −45°C and −60°C, the same formal dependence on monomer concentration. The dependence on the catalyst concentration is approximately but not exactly of a third order.

inorganic chemicalsMaterials sciencePolymers and Plasticsorganic chemicalsCationic polymerizationSolution polymerizationGeneral ChemistryCondensed Matter PhysicsStyreneCatalysischemistry.chemical_compoundChain-growth polymerizationMonomerchemistryPolymer chemistryMaterials ChemistryIonic polymerizationPolymer Bulletin
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Formation and characterization of oxidic and metallic Fe/Ni multilayers prepared from Langmuir-Blodgett films

1994

Oxidic and metallic iron, nickel, and mixed iron/nickel mono- and multilayers were prepared by some treatments of iron- and nickel-containing Langmuir-Blodgett films. The layers were characterized by several surface-sensitive methods. Interactions between the iron and the nickel could be observed. The results are different to those obtained from disordered bulk alloys and from simple diffusion calculations.

inorganic chemicalsNuclear and High Energy PhysicsMolecular diffusionMaterials scienceInorganic chemistrytechnology industry and agriculturechemistry.chemical_elementCondensed Matter PhysicsLangmuir–Blodgett filmAtomic and Molecular Physics and OpticsCharacterization (materials science)MetalNickelchemistryvisual_artotorhinolaryngologic diseasesvisual_art.visual_art_mediumPhysical and Theoretical ChemistryHyperfine Interactions
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Tailoring polymers through interplay of ligands within precatalysts: 8-(Nitro/benzhydryl-arylimino)-7,7-dimethyl-5,6-dihydroquinolylnickel halides in…

2017

A series of 8-(nitro/benzhydryl-substituted arylimino)-7,7-dimethyl-5,6-dihydroquinolines and the corresponding nickel halide complexes were synthesized and characterized. Molecular structures of representative nickel complexes were determined by single crystal X-ray diffraction, showing the dinuclear dimers with distorted square-pyramidal geometry around the nickel center. The binding energies determined by X-ray photoelectron spectroscopy (XPS) indicate the effective coordination between the sp2-nitrogen and nickel atoms as well as the influence of both the halogen ligands and the substituents within dihydroquinolines on the strength of the NiN bond. Ethylene polymerization with the nicke…

inorganic chemicalsPolymers and PlasticsMethylaluminoxaneSubstituentHalidechemistry.chemical_element010402 general chemistry01 natural sciencesvinylene groupnickelchemistry.chemical_compoundBromideVinylene groupPolymer chemistryMaterials ChemistryOrganic chemistrynitro substituent010405 organic chemistryChemistryLigandOrganic Chemistryhomogeneous catalysis0104 chemical sciencesNickelPolymerizationpolymerization
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Nature of activating effect of two-step polymerization of propylene

1999

The prepolymerization effect on propylene polymerization in the presence of a TiCl 3 -based catalyst, modified by di-n-buthyl ether, was studied. The influence of prepolymerization on the electron spin resonance spectra and morphology of the catalyst, as well as the properties and the morphology of both prepolymer and regular polymerization products, was investigated. The polymer morphology was evaluated through scanning electron microscopy, polymer bulk density, and particle size distribution. Some evidence of the enhancement effect of prepolymerization on the catalyst activity and stereospecificity was obtained. No influence from prepolymerization was observed on molecular weight and its …

inorganic chemicalsPolypropylenechemistry.chemical_classificationPolymers and PlasticsScanning electron microscopeorganic chemicalsGeneral ChemistryPolymerSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundCrystallinitychemistryChemical engineeringPolymerizationPolymer chemistryMaterials Chemistryheterocyclic compoundsZiegler–Natta catalystPrepolymerJournal of Applied Polymer Science
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Nature of cobalt active species in hydrodesulfurization catalysis: combined support and preparation method effects

2007

Abstract Co/γ-Al2O3, Co/SiO2, Co/MCM-41, Co/ASA and Co/S2 (amorphous aluminosilicate with Al/Si = 0.13 and with Al/Si ≈ 2, respectively) were prepared by the method of wet impregnation and by the method of precipitation in the presence of sodium carbonate. The samples were characterised by XPS, XRD and TPR. The catalytic activity was tested in the hydrodesulfurization of thiophene using a continuous flow reactor. Among the wet impregnated catalysts those supported on the amorphous and ordered mesoporous silica exhibited higher HDS activity as compared to the alumina containing supports. Particularly, the use of the mesoporous, high surface area MCM-41 support, determined the best performing…

inorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementMesoporous silicaCatalysisCatalysischemistry.chemical_compoundchemistryMCM-41Physical and Theoretical ChemistrySodium carbonateMesoporous materialHydrodesulfurizationCobaltNuclear chemistry
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Combined effect of noble metals (Pd, Au) and support properties on HDS activity of Co/SiO2 catalysts

2009

Abstract Cobalt-based catalysts supported on different types of SiO 2 are studied in the hydrodesulfurization of thiophene. Amorphous silica and siliceous MCM-41 and HMS, characterized by different texture and surface acidity are used as carriers. The effects due to the modification of the support by impregnation with palladium precursor and to the co-impregnation of cobalt and gold are considered. The catalysts are characterized by N 2 physisorption (BET), XRD, TPR and XPS techniques. The use as supports of the ordered mesoporous silica with higher surface area with respect to amorphous silica, produces a better dispersion of the cobalt oxides particles. Moreover, the addition of palladium…

inorganic chemicalsProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementMesoporous silicaCatalysisCatalysischemistry.chemical_compoundchemistryCrystalliteHydrodesulfurizationTetrahydrothiopheneCobaltCobalt oxidePalladiumApplied Catalysis A: General
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Ni(II) and Pd(II) complexes of camphor-derived diazadiene ligands: steric bulk tuning and ethylene polymerization

1998

Abstract Nickel(II) and palladium(II) centers were coordinated to a series of chiral 1,4-diazadiene ligands. The ligand backbones are camphor derivatives and the imine nitrogens are attached to independently varied 2- and 2,6-substituted aryl groups. Upon activation with methyl-aluminoxane, the dibromo nickel complexes polymerize ethylene and 1-hexene. The polymerization properties are dependent on the steric features of the aryl substituents on the imine nitrogens.

inorganic chemicalsSteric effectsEthyleneChemistryLigandArylIminechemistry.chemical_elementPhotochemistryInorganic Chemistrychemistry.chemical_compoundNickelPolymerizationPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryPalladiumInorganic Chemistry Communications
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Impact of α,β-dehydroamino acid residues on the binding abilities of di-, tri- and tetra-peptides

2000

Insertion of a dehydroamino acid residue into a sequence of di-, tri- or tetra-peptide changed considerably the binding abilities of peptide ligands towards copper(II) ions. Potentiometric and spectroscopic (EPR, UV-VIS and CD) data have shown that the amide nitrogen of the dehydroamino acid residue is more effective in co-ordination than its parent analogue. In the case of the bulky ΔPhe residue also the (Z–E) isomerisation has a critical impact on the co-ordination equilibria in the system studied.

inorganic chemicalsbiologyStereochemistryPotentiometric titrationchemistry.chemical_elementGeneral Chemistrybiology.organism_classificationCopperCatalysislaw.inventionchemistry.chemical_compoundResidue (chemistry)chemistrylawAmideMaterials ChemistryTetraElectron paramagnetic resonanceIsomerizationPeptide ligandNew Journal of Chemistry
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Efficient ethylene polymerisation catalysis by a cationic benzyl hafnium complex containing pyrrolide-imine ligandsElectronic supplementary informati…

2002

A dibenzyl hafnium(IV) complex containing pyrrolide-imine chelate ligands was synthesized and investigated as an ethylene polymerisation catalyst.

inorganic chemicalschemistryEthylene polymerizationPolymer chemistryCationic polymerizationchemistry.chemical_elementOrganic chemistryChelationGeneral ChemistryImine ligandsHafniumCatalysisJournal of the Chemical Society, Dalton Transactions
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Facile Synthesis of Fluorescent Polymer Nanoparticles by Covalent Modification-Nanoprecipitation of Amine-Reactive Ester Polymers

2015

Emission wavelength control in fluorescent nanoparticles (NPs) is crucial for their applications. In the case of inorganic quantum dots or dye-impregnated silica NPs, such a control is readily achieved by changing the size of the particles or choosing appropriate fluorescent dyes, respectively. A similar modular approach for controlling the emission wavelength of fluo-rescent polymer NPs, however, is difficult. This article reports on fluorescent polymer NPs, the synthesis of which provides a platform for a modular approach towards the preparation of fluorescent NPs of desired emission wavelength. Atom-transfer radical polymerization (ATRP) is employed to synthesize reactive ester polymers,…

inorganic chemicalschemistry.chemical_classificationMagnetic Resonance SpectroscopyMaterials sciencePolymers and PlasticsPolymersAtom-transfer radical-polymerizationOrganic ChemistryDispersityRadical polymerizationtechnology industry and agricultureNanoparticleQuantum yieldEstersPolymerrespiratory systemPhotochemistryFluorescencePolymerizationchemistryQuantum dotMaterials ChemistryNanoparticlesAminesFluorescent DyesMacromolecular Rapid Communications
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