Search results for "catalyst"

Effect of Pre-Reduction on the Properties and the Catalytic Activity of Pd/Carbon Catalysts: A Comparison with Pd/Al2O3

2013

The effect of pre-reduction in solution with chemical reagents on the catalytic performance and catalyst properties of Pd/carbon catalysts was systematically investigated with a multitechnique approach. The results are critically discussed in comparison to those recently obtained on analogous Pd/alumina catalysts. It was proved that the Pd phase on the carbon surface is characterized by a high mobility, opposite to what occurs on alumina. As a result, the Pd particles on carbon aggregate together during pre-reduction, with a consequent decrease in available metal surface. Pd particles remain aggregated also in reaction conditions; the decreased Pd dispersion negatively affects the catalyst …

AC3-Symmetric Palladium Catalyst with a Phosphorus-Based Tripodal Ligand

2006

Rare Earth Metal Catalysts

2003

Two-step polymerization of propylene over MgCl2-supported titanium catalyst

1998

The prepolymerization effect on propylene polymerization in the presence of a MgCl 2 -supported titanium catalyst was studied. The catalyst was pre-activated by polymerizing a small amount of propylene in the presence of Et 3 Al and cyclohexylmethyldimethoxysilane under mild conditions, and then it was used in a second step of propylene polymerization. Comparative studies of the polymerization process involving the investigated catalyst and its unmodified counterpart showed the rate-enhancement effect of prepolymerization and the same molecular weights, MWD's and isotacticities of the polymers obtained. Concentrations of active sites and propagation rate as well as transfer rate constants w…

2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides: Synthesis, characterization and ethylene oligomerization

2017

Abstract 2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides (Ni1–Ni8) were synthesized from the respective ligands L1–L8 and characterized. Upon activation with either methylaluminoxane (MAO) or ethylaluminium sesquichloride (EASC), they show high catalytic activity of up to 10.84 × 106 g(oligomer) mol− 1(Ni) h− 1 in ethylene oligomerization. The products range from butenes to dodecenes for Ni1–Ni4, but are limited to butenes and hexenes in the case of Ni5–Ni8. DFT calculations indicate that the Ni C bond length in the model alkyl complexes depends both on the nature of the substituents at the heterocycles and the kind of the alkyl group, shedding some light on the…

Biphasic ethylene polymerisation using ionic liquid over a titanocene catalyst activated by an alkyl aluminium compound

2007

Abstract 1-n-Butyl-3-methylimidazolium tetrachloroaluminate ([BMIM]+[AlCl4]−) was applied to biphasic ionic liquid/hexane ethylene polymerisation as a medium of the Cp2TiCl2 titanocene catalyst activated by alkylaluminium compounds (MAO, AlEt2Cl, AlEt3). The best results were obtained using AlEt2Cl. The results show that catalyst recycling, higher ethylene pressure, and greater Al/Ti molar ratio along with a greater volume of the ionic liquid phase enhance catalyst activity. The polyethylene gathered from the hexane phase is characterised primarily by its high purity. Its physical properties remain polyethylene obtained over a heterogeneous metallocene catalyst. Thus, biphasic ionic liquid …

Practical Synthesis of Vinyl-Substitutedp-Phenylenevinylene Oligomers and Their Triethoxysilyl Derivatives

2001

Luminescent semiconducting organic compounds are widely used as active layers in electro-optical devices. Apart from conjugated polymers, monodisperse oligomers also represent attractive materials. The synthesis of stilbenoid oligomers with polymerizable end groups is presented. Oligo(phenylenevinylene)s with terminal vinyl groups 17–19 are prepared in good yields by Horner–Emmons olefinations or by the Heck reaction of the iodo-substituted oligomers 15, 16 with compressed ethene. Triethoxysilyl groups can be linked via rigid 1,2-vinylene units to the chromophores 26–30, either in the direct reaction of 14, 24 with silanes 21, 22 or by cross-metathesis of 17–19 with the vinylsilanes 21, 22 …

Electrocatalytic Properties of Carbosilane‐Based Hyperbranched Polymers Functionalized with Interacting Ferrocenyl Units

2012

Two types of hyperbranched ferrocene-containing polycarbosilanes were obtained by hydrosilylation of polydiallylmethylsilane (hb-PDAMS) and polymethyldiundecenylsilane (hb-PMDUS) with diferrocenylmethylsilane. The redox properties of both polymers have been investigated both in solution and confined onto platinum electrodes. The electrocatalytic activity of polymer-modified electrodes toward the reduction of oxygen as well as the electrochemical reduction and oxidation of hydrogen peroxide has been examined.

Electrochemical study on a tricyclic 1,1,1-tricar-bonyl-2,3-1 diazaferrole derivative. II. Activation of carbon monoxide replacement by electron tran…

1986

Etudes, par voltammetrie cyclique, de la reduction electrochimique du complexe de diazaferratricyclodecene, en presence de P(OMe) 3

First Evidence of Proline Acting as a Bifunctional Catalyst in the Baylis–Hillman Reaction Between Alkyl Vinyl Ketones and Aryl Aldehydes

2008

Proline in the presence of sodium hydrogen carbonate has been found to be an effective catalyst for the Baylis–Hillman reaction between methyl or ethyl vinyl ketone and aryl aldehydes. Screening of several amine catalysts showed that an ionizable carboxylic function directly linked to the secondary amine catalyst plays an important role in the synthesis of the desired product in good yield. The data obtained has allowed us to suggest, for the first time, that proline, sarcosine, pipecolinic acid and homoproline may act as bifunctional catalysts via a bicyclic enaminolactone species as intermediate. Quantum-mechanical calculations (PM3/COSMO and ab initio 3-21G/COSMO) support this mechanism …