Search results for "Lene"
showing 10 items of 4480 documents
Synthesis of branched polyethylenes by the tandem catalysis of silica-supported linked cyclopentadienyl-amido titanium catalysts and a homogeneous di…
2003
The synthesis of branched polyethylenes by ethylene polymerization with new tandem catalyst systems consisting of methylaluminoxane-preactivated linked cyclopentadienyl-amido titanium catalysts [Ti(η5:η1-C5Me4SiMe2NR)Cl2 (R = Me or tBu)] supported on pyridylethylsilane-modified silica (PySTiNMe and PySTiNtBu) and homogeneous dibromo nickel catalyst having a pyridyl-2,6-diisopropylphenylimine ligand (PyminNiBr2) in the presence of modified methylaluminoxane was investigated. Ethylene polymerization with only PyminNiBr2 yielded a mixture of 1- and 2-olefin oligomers with methyl branches [weight-average molecular weight (Mw) ∼ 460)] with a ratio of about 1:7. By the combination of this nickel …
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.
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.
On the effect of the nature of counterions on the self-assembly of polyoxyethylene alkyl ether carboxylic acids
2020
In this contribution, we investigate the effect of the type of counterion on the properties of dilute solutions of polyoxyethylene alkyl ether carboxylic acids. Two different surfactants, presenting an oleic acid alkyl chain and on-average five and nine ethylene oxide units, and terminated by a weakly anionic carboxymethyl group were studied. The surfactants were gradually ionized with sodium hydroxide, arginine, and choline hydroxide. The solutions properties were probed by light scattering, electrophoretic mobility, density and sound velocity measurements, as well as by small-angle neutron scattering. To our initial surprise, no specific effect arising from the nature of the counterion co…
Titanium (IV) chloride complexes with salen ligands supported on magnesium carrier: Synthesis and use in ethylene polymerization
2009
The magnesium support with the formula MgCl 2 (THF) 0.32 (Et 2 AlCl) 0.36 was used for immobilization of salen complexes of titanium [Ti(salen)Cl 2 , Ti(salen(O-Me) 2 )Cl 2 ]. The effects of the catalyst composition (i.e. type of titanium complex and type of activator), polymerization temperature, polymerization time, and the effect of comonomer (1-octene) on the activity of the obtained supported catalysts, on the polymer characteristics (molecular weight, molecular weight distribution, melting point), and on the polymer morphology were studied. The findings were compared to those obtained for corresponding unsupported systems. Catalysts immobilization results in considerable changes in ca…
Linear Triphosphines as Ligands for Metal Complexes Immobilization in Ionic Liquids: Palladium-Catalyzed Methoxylation of Alkynes
2012
Several novel palladium triphosphine complexes have been synthesized and tested as recyclable catalysts for the methoxylation of alkynes into acetals in ionic liquids. A complete conversion of phenylacetylene was achieved with only 0.2% of (Pd(Triphos)NCMe)((PF6)2) in a methanol/(BMIM)(BF4) mixture. We discovered that the addition of an ionic liquid to methanol allowed not only to increase the activity of the palladium catalyst but also to provide a recyclable catalyst which can be reused several times with a weaker drop of activity. To complete these catalytic studies, we describe the synthesis of the first poor -electron-donating/strong -electron-acceptor linear Triphosphine which, afte…
Total oxidation of naphthalene using bulk manganese oxide catalysts
2013
Several Mn2O3 catalysts have been synthesized using different preparation methods and tested for the total oxidation of naphthalene, a model polycyclic aromatic compound. The catalysts have been characterized by several physico-chemical techniques such as XRD, TPR, XPS, EDX and TEM. The surface area of the catalyst seems to be of paramount importance, since the mass normalized activity of catalysts increases as the surface area of the Mn2O3 catalysts increases. Consequently, a high surface area ordered mesoporous Mn2O3 catalyst, obtained through a nanocasting route using mesoporous KIT-6 silica as a hard template, was the most efficient catalyst for the deep oxidation of naphthalene. In add…
Novel supramolecular affinity materials based on (−)-isosteviol as molecular templates
2013
The readily available ex-chiral-pool building block (−)-isosteviol was combined with the C3-symmetric platforms hexahydroxytriphenylene and hexaaminotriptycene providing large and rigid molecular architectures. Because of the persistent cavities these scaffolds are very potent supramolecular affinity materials for head space analysis by quartz crystal microbalances. The scaffolds serve in particular as templates for tracing air-borne arenes at low concentration. The affinities of the synthesized materials towards different air-borne arenes were determined by 200 MHz quartz crystal microbalances.
CCDC 1952457: Experimental Crystal Structure Determination
2020
Related Article: Francisco Estevan, Marta Feliz|2020|Dalton Trans.|49|4528|doi:10.1039/C9DT04821A
Nośnikowy katalizator wanadocenowy z udziałem cieczy jonowych w polimeryzacji etylenu
2018
W pracy zsyntezowano szereg układów SILP z katalizatorem wanadocenowym – Cp2VCl2 poprzez immobilizację cieczy jonowych na różne rodzaje krzemionek, różniących się powierzchnią właściwą i wielkością porów, które modyfikowano wybranym związkiem glinoorganicznym – AlEtCl2 lub AlEt2Cl. Zsyntezowane układy analizowano metodami: FTIR, analiza elementarna, BET, AAS i SEM. Każdy z otrzymanych układów SILP był aktywny w polimeryzacji etylenu, niezależnie od ilości i rodzaju zastosowanego aktywatora (AlEtCl2 lub AlEt2Cl). Najwyższą aktywność w polimeryzacji etylenu osiągnięto wobec układu SILP z udziałem krzemionki o bardzo regularnej morfologii, gdzie do utworzenia etylochloroglinianowych anionów pi…