Search results for "ethylene oligomerization"

showing 4 items of 4 documents

Input of P, N-(phosphanyl, amino)-ferrocene hybrid derivatives in late transition metals catalysis

2018

International audience; Unequally functionalized ferrocenes give access to valuable hemilabile reactivity in catalytic reaction. We address the synthesis of hybrid (P, N)-ferrocenyl compounds for which recent catalytic breakthrough applications have been reported, transversely in late transition metals chemistry. Palladium, nickel, rhodium, iridium, and emerging iron and gold catalysis are illustrated from selected examples, which include CC bond formation from cross-coupling and polymerization, allylic substitution, cyanation, hydroformylation, CH arylation and silylation and hydrogenation reactions.

Allylic rearrangementnickel-complexesAminophosphinesethylene oligomerizationchemistry.chemical_elementHomogeneous catalysispbeta-ketoestersCyanation[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryn ligands01 natural sciencesRhodiumCatalysisInorganic ChemistryPolymer chemistryoxazoline-containing ligandsMaterials ChemistryOrganic chemistry[CHIM]Chemical SciencesReactivity (chemistry)Physical and Theoretical ChemistryPolyfunctionalized ligandsferrocenyl ligands010405 organic chemistryasymmetric catalysisHemilabile hybridsHomogeneous catalysischiral ligandssimple ketones0104 chemical scienceschemistrystructural-characterizationFerroceneHydroformylationPalladiumLate transition metals
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Propyl substituted 4-arylimino-1,2,3-trihydroacridylnickel complexes: Their synthesis, characterization and catalytic behavior toward ethylene

2015

Propyl substituted 4-arylimino-1,2,3-trihydroacridylnickel dihalide complexes were designed and prepared by metal-induced template reaction with NiCl2 center dot 6H(2)O or (DME)NiBr2. They were characterized by infrared spectroscopy and elemental analysis. Single crystal X-ray crystallography of representative complex Ni3 revealed a distorted trigonal bipyramidal geometry around nickel. The catalytic activities of the title nickel complexes were negatively affected by propyl substituent on their backbone when comparing with the results by unsubstituted ones. With the activation of diethylaluminium chloride, all nickel complexes exhibited moderate activity (up to 5.10 x 10(5) g mol(-1)(Ni) h…

Diethylaluminium chlorideEthyleneStereochemistryOrganic ChemistrySubstituentchemistry.chemical_elementInfrared spectroscopyBiochemistryMedicinal chemistryCatalysis2-propyl-4-arylimino-1Inorganic ChemistryNickelchemistry.chemical_compoundTemplate reactionTrigonal bipyramidal molecular geometrychemistryMaterials Chemistry3-dihydroacridine; Nickel complex; Ethylene oligomerizationPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Ethylene oligomerization with 2-hydroxymethyl-5,6,7-trihydroquinolinyl-8-ylideneamine-Ni(II) chlorides

2021

Abstract A series of Ni complexes of the general formula [2-(MeOH)-8-{N(Ar)}C9H8N]NiCl2, where Ar = 2,6-Me2C6H3 in Ni1; 2,6-Et2C6H3 in Ni2; 2,6-i-Pr2C6H3 in Ni3; 2,4,6-Me3C6H2 in Ni4; 2,6-Et2-4-MeC6H2 in Ni5 and 2,4,6-t-Bu3C6H2 in Ni6 has been synthesized and characterized by elemental analysis and IR spectroscopy. On activation with MMAO or Et2AlCl, these complexes showed high activity in ethylene oligomerization, reaching 2.23 × 106 g·mol–1 (Ni) h–1 at 30 °C with the Al/Ni ratio of 5500 and 9.11 × 105 g·mol–1 (Ni) h–1 with the Al/Ni of 800, respectively. Moreover, the content of α-C4 indicated high selectivity exceeding 99% in the Ni/Et2AlCl system. Comparing with the previous report by o…

Steric effectsEthyleneSubstituentInfrared spectroscopy010402 general chemistryCo-catalyst01 natural sciencesBiochemistryMedicinal chemistryInorganic ChemistryMetalchemistry.chemical_compoundSubstituent effectEthylene oligomerizationMaterials ChemistryHydroxymethylSelectivityPhysical and Theoretical ChemistryNickel complexes010405 organic chemistryChemistryLigandOrganic Chemistry0104 chemical sciencesActivityElemental analysisvisual_artvisual_art.visual_art_mediumJournal of Organometallic Chemistry
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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…

chemistry.chemical_classificationEthylene010405 organic chemistryethylene oligomerizationProcess Chemistry and TechnologyMethylaluminoxaneGeneral ChemistryPolyethylene010402 general chemistry01 natural sciencesOligomerMedicinal chemistryCatalysis0104 chemical sciencesCatalysisBond lengthnickel precatalystchemistry.chemical_compoundchemistrysubstituent influenceEthylaluminium sesquichlorideOrganic chemistry7-Aryliminocyclopenta[b]pyridineAlkylCatalysis Communications
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