0000000000422291

AUTHOR

Abderrafia Hafid

showing 4 related works from this author

Organolanthanides, catalysts for specific olefin-diene copolymerization: access to new materials

2001

Abstract Non-hindered ansa dicyclopentadienylallyl complexes of samarium, [(CMe2C5H4)2Sm(allyl)]n, and (CMe2C5H4)2Sm(allyl)L (L=THF or allylLi) polymerize isoprene without an aluminum cocatalyst. The polymerizations are highly stereospecific, affording nearly quantitatively 1–4 trans polyisoprene. In the presence of linear 1-olefins, copolymers are formed, with 6–10% of olefin inserted; the 1–4 trans structure of the polyisoprene chain is not altered, and only one olefin molecule is inserted between two polyisoprene fragments. In the common initiator of these three catalytic systems, the (CMe2C5H4)2Sm(allyl) moiety, only one vacant site would be available. As a consequence of the presence o…

chemistry.chemical_classificationOlefin fiberDieneMechanical EngineeringMetals and Alloyschemistry.chemical_compoundchemistryPolymerizationMechanics of MaterialsPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryMoietyMetalloceneIsopreneAlkylJournal of Alloys and Compounds
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Synthesis and X-ray Crystal Structures of (C5HiPr4)Ln(BH4)2(THF)(Ln = Nd and Sm), Versatile Precursors for Polymerization Catalysts

2000

The new half metallocenes [(C5HiPr4)Ln(BH4)2(THF)] [Ln = Sm (1) and Nd (2)], and [(C5HiPr4)U(BH4)3] (3) have been synthesized. The crystal structures of 1 and 2 and of the metallocenes [(C5HiPr4)2Ln(BH4)] [Ln = Sm (4) and Nd (5)] have been determined. The substitution of the BH4 groups of 1 and 2 by a nitrogen-based ligand is possible. In the presence of butyllithium, these complexes show an activity in isoprene and styrene polymerization.

LanthanideChemistryLigandInorganic chemistrychemistry.chemical_elementCrystal structureStyreneInorganic Chemistrychemistry.chemical_compoundCrystallographyPolymerizationButyllithiumBoronIsopreneEuropean Journal of Inorganic Chemistry
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Organometallic early lanthanide clusters: syntheses and X-ray structures of new monocyclopentadienyl complexes.

2004

The reaction of Ln(BH(4))(3)(THF)(3) or LnCl(3)(THF)(3) with 1 equiv of KCp*' ligand (Cp' = C(5)Me(4)n-Pr) afforded the new monocyclopentadienyl complexes Cp*'LnX(2)(THF)(n) (X = BH(4), Ln = Sm, n = 1, 1a, Ln = Nd, n = 2, 1b; X = Cl, Ln = Sm, n = 1, 3a) and [Cp*'LnX(2)](n') (X = BH(4), n' = 6, Ln = Sm, 2a, Ln = Nd, 2b; X = Cl, Ln = Nd, 4b). All these compounds were characterized by elemental analysis and (1)H NMR. Crystals of mixed borohydrido/chloro-bridged [Cp*'(6)Ln(6)(BH(4))(12-x))Cl(x)(THF)(n')] (x = 10, n' = 4, Ln = Sm, 2a', Ln = Nd, 2b'; x = 5, n = 2, Ln = Sm, 2a' ') were also isolated. Compounds 2a, 2b, 2a', 2b', and 2a'' were structurally characterized; they all exhibit a hexameric…

Inorganic ChemistryLanthanideCrystallographychemistry.chemical_compoundStereochemistryChemistryX-raySolid-stateProton NMRPhysical and Theoretical ChemistryBorohydrideAdductInorganic chemistry
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Nouveaux complexes organométalliques monocyclopentadiényles de lanthanides

2005

[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistry[CHIM.COOR] Chemical Sciences/Coordination chemistry
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