Search Results - "Hessen, Bart"
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Lanthanum Tribenzyl Complexes as Convenient Starting Materials for Organolanthanum Chemistry
Published in Organometallics (03-07-2006)“…Simple tribenzyl complexes of lanthanum, [La(CH2C6H4-4-R)3(THF)3] (R = H (1a), Me (1b)), were prepared in a remarkably straightforward fashion from LaBr3(THF)4…”
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Palladium-Catalyzed Enantioselective Conjugate Addition of Arylboronic Acids
Published in Organic letters (10-11-2005)“…The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to α,β-unsaturated aldehydes, ketones, and esters is described. For cyclic…”
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One Ligand Fits All: Cationic Mono(amidinate) Alkyl Catalysts over the Full Size Range of the Group 3 and Lanthanide Metals
Published in Journal of the American Chemical Society (04-08-2004)“…Using a sterically demanding amidinate ancillary ligand and an in situ alkylation procedure, neutral mono(amidinate) dialkyl and cationic mono(amidinate)…”
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Versatile Coordination of Cyclopentadienyl-Arene Ligands and Its Role in Titanium-Catalyzed Ethylene Trimerization
Published in Journal of the American Chemical Society (15-04-2009)“…Cationic titanium(IV) complexes with ansa-(η5-cyclopentadienyl,η6-arene) ligands were synthesized and characterized by X-ray crystallography. The strength of…”
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Electronic Selectivity Tuning in Titanium(III)-Catalyzed Acetylene Cross-Dimerization Reactions
Published in Organometallics (28-11-2011)“…The reactivity of open-shell titanium(III) complexes in organometallic catalysis is associated with many open questions, in particular regarding the…”
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Synthesis and Structures of Scandium and Lutetium Benzyl Complexes
Published in Organometallics (14-04-2008)“…Scandium and lutetium benzyl complexes were prepared. Reaction of [ScCl3(THF)3] with potassium benzyl afforded [Sc(CH2Ph)3(THF)3] (1). In the solid state the…”
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Highly active/selective and adjustable zirconium polymerization catalysts stabilized by aminopyridinato ligands
Published in Journal of organometallic chemistry (01-10-2007)“…Sterically very demanding aminopyridinato ligands stabilize thermally robust, highly active and selective zirconium ethylene polymerization catalysts. Small…”
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Neutral and Cationic Alkyl and Alkynyl Complexes of Lanthanum: Synthesis, Stability, and Cis-Selective Linear Alkyne Dimerization
Published in Organometallics (01-03-2004)“…Neutral triazacyclononane−amide lanthanum dialkyl and dialkynyl complexes were synthesized and structurally characterized. A cationic triazacyclononane−amide…”
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Application of Monodentate Secondary Phosphine Oxides, a New Class of Chiral Ligands, in Ir(I)-Catalyzed Asymmetric Imine Hydrogenation
Published in Organic letters (01-05-2003)“…Secondary phosphine oxides were prepared from R1PCl2 and R2MgBr, followed by hydrolysis. They were obtained in an enantiopure form by preparative chiral HPLC…”
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Thermolysis of Half-Sandwich Vanadium(V) Imido Complexes to Generate Vanadium(III) Imido Species via a Vanadium(IV) Intermediate
Published in Organometallics (13-12-2010)“…Thermolysis of half-sandwich vanadium imido complexes Cp(RN)V(i-Pr2N)Me (R = p-Tol, 1a; R = t-Bu, 1b) results in a mixture of products, including vanadium(IV)…”
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1,1‘-Diisocyanoferrocene and a Convenient Synthesis of Ferrocenylamine
Published in Organometallics (08-01-2001)“…The new ferrocene derivative 1,1‘-diisocyanoferrocene was prepared in 50% isolated yield from the reaction of 1,1‘-diisocyanatoferrocene with formic acid…”
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Highly enantioselective rhodium-catalyzed conjugate addition of arylboronic acids to enones at room temperature
Published in Tetrahedron letters (17-10-2005)“…The rhodium–phosphoramidite-catalyzed asymmetric conjugate addition of arylboronic acids to enones proceeds at room temperature using [Rh(OH)(cod)] 2 or…”
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Mono(amidinate) Yttrium Alkyl Complexes: The Effect of Ligand Variation on Ethene Polymerization Catalysis
Published in Zeitschrift für anorganische und allgemeine Chemie (1950) (01-09-2006)“…Yttrium dialkyl complexes were prepared for three different 2,6‐diisopropylphenyl‐substituted benzamidinate ligands. The electron‐donating ability of the…”
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Relative Reactivity of the Metal−Amido versus Metal−Imido Bond in Linked Cp-Amido and Half-Sandwich Complexes of Vanadium
Published in Organometallics (25-08-2008)“…Treatment of (η5-C5H4C2H4NR)V(N-t-Bu)Me (R = Me, i-Pr) and CpV(N-p-Tol)(N-i-Pr2)Me (Cp = η5-C5H5) with B(C6F5)3 or [Ph3C][B(C6F5)4] results in formation of the…”
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Synthesis, Structure, and Reactivity of Rare-Earth Metallocene η3-Propargyl/Allenyl Complexes
Published in Organometallics (10-11-2008)“…The reaction of the alkyl complexes Cp*2LnCH(SiMe3)2 (Ln = Y 1-Y, Ce 1-Ce, La 1-La; Cp* = η5-C5Me5) and Me2Si(η5-C5Me4)2LnCH(SiMe3)2 (Ln = Ce 5-Ce) with…”
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Highly Efficient Hydrosilylation of Alkenes by Organoyttrium Catalysts with Sterically Demanding Amidinate and Guanidinate Ligands
Published in Organometallics (14-07-2008)“…The sterically demanding guanidine ArNHC(NMe2)NAr (Ar = 2,6-diisopropylphenyl, HL) reacts with Y(CH2SiMe3)3(THF)2 to give the yttrium dialkyl complex…”
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Scandium, Yttrium, and Lanthanum Benzyl and Alkynyl Complexes with the N-(2-Pyrrolidin-1-ylethyl)-1,4-diazepan-6-amido Ligand: Synthesis, Characterization, and Z-Selective Catalytic Linear Dimerization of Phenylacetylenes
Published in Organometallics (09-02-2009)“…1,4,6-Trimethyl-N-(2-pyrrolidin-1-ylethyl)-1,4-diazepan-6-amine (HL) reacts with M(CH2Ph)3(THF)3 to give the dibenzyl complexes (L)M(CH2Ph)2 (M = Sc, 1; M = Y,…”
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Pentamethylcyclopentadienyl Zirconium and Hafnium Polyhydride Complexes: Synthesis, Structure, and Reactivity
Published in Organometallics (16-04-2001)“…The half-sandwich zirconium and hafnium N,N-dimethylaminopropyl complexes Cp*M[(CH2)3NMe2]Cl2 (Cp* = η5-C5Me5, M = Zr, 1; Hf, 2) and Cp*M[(CH2)3NMe2]2Cl (M =…”
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Reversible Chain Transfer between Organoyttrium Cations and Aluminum: Synthesis of Aluminum-Terminated Polyethylene with Extremely Narrow Molecular-Weight Distribution
Published in Chemistry : a European journal (04-12-2006)“…Aminopyridinato‐ligand‐stabilized organoyttrium cations are accessible in very good yield through alkane elimination from trialkyl yttrium complexes with…”
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