685859-40-9Relevant articles and documents
Tribenzyl Tantalum(V) Complexes of Amine Bis(phenolate) Ligands: Investigation of α-Abstraction vs Ligand Backbone β-Abstraction Paths
Groysman, Stanislav,Goldberg, Israel,Kol, Moshe,Genizi, Elisheva,Goldschmidt, Zeev
, p. 1880 - 1890 (2008/10/09)
The synthesis, structure, and reactivity of tribenzyl Ta(V) complexes of amine bis(phenolate) ligands were investigated as a function of the ligands' structure: i.e., the steric bulk of the phenolate substituents and the presence of a side arm donor. The tribenzyl complexes were prepared by toluene-elimination reactions of Ta(CH2Ph)5 with the ligand precursors. They were found to be of octahedral mer geometry, with the side-arm donor (if present) unbound. These complexes underwent two well-defined toluene elimination reactions determined by the structural features of the ligands. An α-abstraction reaction, leading to alkyl-alkylidene complexes, occurred only if the phenolate ortho substituents were small (H, Cl) and a side-arm donor was present. Bulkier phenolate substituents (Me) or the lack of a side-arm donor led to a β-abstraction process from the ligand backbone, forming a dibenzyl complex with a metallaazacyclopropane ring. The side-arm donor, if present, was found to bind to the metal in both paths. A bulkier ligand precursor having t-Bu groups on the two phenolate rings did not react with Ta(CH2Ph)5 at room temperature, whereas an asymmetric half-bulky ligand precursor carrying a Me group and a t-Bu group on the two rings led directly to the β-abstraction product.
