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Organometallics: Materials and Catalysis team
Abstract
This research PhD work deals with the functionalization and applications of the closo-decahydrido-decaborate cluster, through novel palladium mediated substitution and iron catalyzed reactions. In a first part, an efficient synthetic route for the preparation of phosphine substituted the closo-decahydrido-decaborate cluster by the substitution of apical iodine in [N(n C4H9)4]2[1 B10H9I] with tertiary phosphine ligands was selectively achieved in apical position, leading to the monoanionic cluster [N(nC4H9)4][1-B10H9PR3]. This reaction was promoted by Pd(0) phosphine complexes Pd(PR3)n (R = alkyl, aryl) at a mild temperature (50°C) with high yields up to 90%. These new phosphine borate clusters were fully characterized notably by X-ray crystal diffraction. This work provides an additional example of efficient synthetic routes for modifying closo-decahy-drido-decaborate clusters. In a second part, a series of original iron based complexes, [FeL₃][B₁₀H₁₀] were synthesized and fully cha-racterized starting from [NEt3H]2[B₁₀H₁₀] cluster FeX2 salts, and azoheterocyclic ligands [1,10-phenanthroline, 2,2’- bipyridydine, 4,7-dimethyl-1,10-phenanthroline, 2,9-dimethyl-1,10-phen-anthroline, 5-nitro-1,10-phenanthroline, 5-ami-no-1,10-phenanthroline and 4,4-di-methyl-2,2-bipyridine. The catalytic properties of these complexes were then investigated, notably for the efficient homo-coupling of benzylamine derivatives leading to the corresponding imines. This result highlighted the crucial and efficient association iron/[B₁₀H₁₀]2- in catalytic transformations.
Jury
Contact
Christophe Darcel (3 62 71) – [email protected]
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Rennes Métropole
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Un stand-up frontal, introspectif, absurde, toujours humain.
Session en présentiel le 8 décembre 2026 à RENNES
finaliste de la 20ème saison de « La France a un Incroyable Talent »