Reference : New tripodal iminophosphorane-based ethylene oligomerization catalysts - Part II. Cat...
Scientific journals : Article
Physical, chemical, mathematical & earth Sciences : Chemistry
http://hdl.handle.net/2268/15430
New tripodal iminophosphorane-based ethylene oligomerization catalysts - Part II. Catalytic behavior
English
Beaufort, Laurence [> > > >]
Benvenuti, Federica [> > > >]
Delaude, Lionel mailto [Université de Liège - ULg > Département de chimie (sciences) > Chimie macromoléculaire et catalyse organique >]
Noels, Alfred mailto [Université de Liège - ULg > Services généraux (Faculté des sciences) > Relations académiques et scientifiques (Sciences) >]
2008
Journal of Molecular Catalysis A : Chemistry
Elsevier Science
283
1-2
77-82
Yes (verified by ORBi)
International
1381-1169
Amsterdam
The Netherlands
[en] Cu complexes ; Fe complexes ; Ni complexes ; Pd complexes ; tripodal ligand
[en] Seven transition-metal complexes of general formula RC(CH2NPR'(3))(3))MX2 based on new tripodal iminophosphorane ligands were investigated as initiators for the oligomerization of ethylene in the presence of aluminum co-catalysts using high-throughput techniques. In all cases, ethylene consumption peaked at ca. 30 degrees C and was not drastically affected by varying the nature of the metal (M = Ni, Fe, Pd, Cu), the aluminum co-catalyst (MMAO, Et2AlCl, or EtAlCl2) or the substituents of the tris(iminophosphorane) ligand (R = Me, Ph; R'= cyclopentyl, Ph). Structural modifications of the organometallic complexes, either at the metal center or within the tripodal ligand, however, had a significant impact on the oligomer distribution obtained. In particular, Pd-based catalyst (PhC(CH2NPPh3)(3))PdCl2 displayed an excellent selectivity toward hexene formation. (c) 2007 Elsevier B.V. All rights reserved.
http://hdl.handle.net/2268/15430
10.1016/j.molcata.2007.12.012

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