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Square-planar dichloro palladium complexes with trans-configurated phosphine ligands avoiding ortho-metallation: Ligand design, complex synthesis, molecular structure and catalytic potential for Suzuki cross-coupling reactions
Auteur(s)
Date de parution
2006
In
J. Organomet. Chem.
Vol.
20
No
691
De la page
4257
A la page
4264
Résumé
The square-planar palladium complexes trans-[PdCl2(PPh2-CH2-2,4,6-C6H2Me3)2] (1) and trans-[PdCl2(?2-PPh2-CH2-2,4,6-C6HMe3-CH2-2,4,6-C6HMe3-CH2-PPh2)] (2) were synthesized from [PdCl2(cod)] (cod = 1,5-cyclooctadiene) and the corresponding new phosphine or diphosphine ligands. The single-crystal x-ray structure anal. reveals for both complexes a trans arrangement of the two chlorine and of the two phosphorus atoms. In both cases, ortho-metalation leading to palladacycles is not possible, since all ortho positions in the benzylic rings of 1 and 2 are blocked by Me substituents. Both complexes catalyze Suzuki cross-coupling reactions of deactivated and even bulky arene substrates. [on SciFinder(R)]
Type de publication
Resource Types::text::journal::journal article
