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Süss-Fink, Georg
Nom
Süss-Fink, Georg
Affiliation principale
Fonction
Professeur ordinaire
Email
georg.suess-fink@unine.ch
Identifiants
Résultat de la recherche
Voici les éléments 1 - 2 sur 2
- PublicationAccès libreSquare-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(2006)
;Chahen, Ludovic; The square-planar palladium complexes trans-[PdCl2 (PPh2-CH2-2,4,6-C6H2Me3)2] (1) and trans-[PdCl2 (η2-PPh2-CH2-2,4,6-C6HMe3-CH2-2,4,6-C6HMe3-CH2-PPh2)] (2) have been synthesized from [PdCl2 (cod)] (cod = 1,5-cyclooctadiene) and the corresponding new phosphine or diphosphine ligands. The single-crystal X-ray structure analysis reveals for both complexes a trans arrangement of the two chlorine and of the two phosphorus atoms. In both cases, ortho-metallation leading to palladacycles is not possible, since all ortho positions in the benzylic rings of 1 and 2 are blocked by methyl substituents. Both complexes are found to catalyze Suzuki cross-coupling reactions of deactivated and even bulky arene substrates. - PublicationAccès libreDouble HCl elimination and configuration change in the square-planar palladium complex trans-[{(Ph2PC6H4CONH) 2C6H4}PdCl2] under Suzuki conditions: Isolation and molecular structure of cis-[{(Ph2PC6H4CON)2C6H4}Pd](2006)
;Chahen, Ludovic ;Karmazin-Brelot, LydiaThe trans-configurated square-planar palladium complex trans-[{(Ph2PC6H4CONH) 2C6H4}PdCl2] (1), which catalyzes the Suzuki cross coupling of 4-bromotoluene with phenylboronic acid, was found to react with potassium carbonate in toluene at 90 °C (Suzuki conditions) to give cis-[{(Ph2PC6H4CON)2C6H4}Pd] (2). The single-crystal X-ray structure analysis of 2 reveals the square-planar palladium center to be in a cis configuration. The trans–cis configuration change at palladium is possible because of the elimination of two HCl equivalents in the conversion of 1 into 2. Both complexes 1 and 2 show approximately the same catalytic performance for Suzuki reactions, suggesting 2 to be the catalytically active species.