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Zeev Goldschmidt

Publications and source records attributed to Zeev Goldschmidt.

2 recordsLinked to original sources

Titanium and zirconium complexes of dianionic and trianionic amine-phenolate-type ligands in catalysis of lactide polymerization.

The synthesis of alkoxotitanium(IV) and -zirconium(IV) complexes of seven chelating tetradentate di- or trianionic amine-phenolate ligands belonging to three families and their application in L-lactide polymerization are described. The isopropoxotitanium complexes were synthesized by a direct reaction between the ligand precursors and titanium tetraisopropoxide, whereas the zirconium complexes were synthesized by various routes. For titanium, complexes of all seven ligands could be synthesized. For zirconium, the hexacoordinate complexes derived from all dianionic ligands were synthesized; however, the only pentacoordinate complex that could be produced was the one derived from the bulky trianionic ligand. X-ray structures of zirconium complexes of the three families indicated a substantial pi donation from the alkoxo ligand to the metal. All complexes were found to be active lactide polymerization catalysts, and their activity was found to depend strongly on the metal, the coordination number around the metal, and the phenolate substituents but not on the ligand backbone.

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Vanadium(III) and vanadium(V) amine tris(phenolate) complexes.

The coordination chemistry of amine tris(phenolate) ligands around V(III) and V(V) is described for the first time. Three amine tris(phenolate) ligands were employed featuring different steric and electronic influence exerted by the phenolate substituents in the ortho and para positions being either t-Bu, Me, or Cl. V(III) complexes of all ligands (1-3) were readily obtained by reaction between the ligand precursors and VCl3(THF)3 in the presence of triethylamine. The complexes obtained were pentacoordinate, a THF ligand completing the coordination sphere of the metal, which was found to be of almost perfect TBP geometry, as revealed by crystallography. V(V) oxo complexes of all the ligands (4-6) were readily obtained by a reaction between the ligand precursors and VO(OPr)3. The oxo complexes of the alkyl-bearing ligands (4 and 5) could also be synthesized by the air oxidation of the corresponding V(III) complexes (1 and 2); however, the attempted air oxidation of the V(III) complex bound to the electron-poor ligand (3) did not yield the corresponding oxo complex 6. 1H NMR and crystallographic analysis of complexes 4 and 5 supported their TBP structures. Complex 6, on the other hand, was found to be composed of a TBP complex (6a) and an octahedral complex (6b) in equilibrium, the octahedral complex being more stable at lower temperatures. An X-ray structure of 6b revealed a mononuclear oxo complex, the sixth coordination site being occupied by an aqua ligand to which two THF molecules are H-bonded. Complexes 4-6 catalyze the epoxidation of olefins by t-BuOOH, albeit slowly. These complexes may thus be considered as structural and functional models of vanadium-dependent haloperoxidase enzymes.

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