Emmanuelle Despagnet-Ayoub
Paul Sabatier University
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Featured researches published by Emmanuelle Despagnet-Ayoub.
Inorganic Chemistry | 2012
Wilfried-Solo Ojo; Kane Jacob; Emmanuelle Despagnet-Ayoub; Bianca K. Muñoz; Sergio Gonell; Laure Vendier; Viet-Hoang Nguyen; Michel Etienne
The synthesis and characterization (mainly by (19)F NMR and X-ray diffraction) of highly fluorinated aryl-4,5,6,7-tetrafluoroindazoles and their corresponding thallium hydrotris(indazolyl)borate complexes are reported [aryl = phenyl, pentafluorophenyl, 3,5-dimethylphenyl, 3,5-bis(trifluoromethyl)phenyl]. Thanks to N-H···N hydrogen bonds, the indazoles crystallize as dimers that pack differently depending on the nature of the aryl group. The thallium hydrotris(indazolyl)borate complexes Tl[Fn-Tp(4Bo,3aryl)] resulting from the reaction of aryl-4,5,6,7-tetrafluoroindazoles [aryl = phenyl, 3,5-dimethylphenyl, 3,5-bis(trifluoromethyl)phenyl] with thallium borohydride adopt overall C(3v) symmetry with the indazolyl groups bound to boron via their N-1 nitrogen in a conventional manner. When the perfluorinated pentaphenyl-4,5,6,7-tetrafluoroindazole is reacted with thallium borohydride, a single regioisomer of C(s) symmetry having one indazolyl ring bound to boron via its N-2 nitrogen, TlHB(3-pentafluorophenyl-4,5,6,7-tetrafluoroindazol-1-yl)(2)(3-pentafluorophenyl-4,5,6,7-tetrafluoroindazol-2-yl) Tl[F27-Tp((4Bo,3C6F5)*)], is obtained for the first time. Surprisingly, the perfluorinated dihydrobis(indazolyl)borate complex Tl[F(18)-Bp(3Bo,3C6F5)], an intermediate on the way to the hydrotris(indazolyl)borate complex, has C(s) symmetry with two indazolyl rings bound to boron via N-2. The distortion of the coordination sphere around Tl and the arrangement of the complexes in the crystal are discussed.
Journal of the American Chemical Society | 2015
Emmanuelle Despagnet-Ayoub; Michael K. Takase; Jay A. Labinger; John E. Bercaw
Addition of trimethylphosphine to a bis(phenolate)benzylimidazolylidene(dibenzyl)zirconium complex induces migration of a benzyl ligand from the metal center to the C(carbine) atom. This process may be reversed, resulting in Csp(3)-Csp(3) activation, by abstraction of the phosphine, an example of regulated, reversible alkyl migration. Addition of ammonia to the dibenzyl complex results in migration of one benzyl group and protonolysis of the other to generate a bis(NH2)-bridged dimer via an NMR-observable intermediate NH3 adduct.
Archive | 2014
Bianca K. Muñoz; Wilfried-Solo Ojo; Kane Jacob; Nuria Romero; Laure Vendier; Emmanuelle Despagnet-Ayoub; Michel Etienne
Related Article: Bianca K. Munoz, Wilfried-Solo Ojo, Kane Jacob, Nuria Romero, Laure Vendier, Emmanuelle Despagnet-Ayoub, Michel Etienne|2014|New J.Chem.|38|2451|doi:10.1039/C4NJ00136B
Journal of the American Chemical Society | 2004
Emmanuelle Despagnet-Ayoub; Robert H. Grubbs
Organometallics | 2005
Emmanuelle Despagnet-Ayoub; Robert H. Grubbs
Organometallics | 2008
Emmanuelle Despagnet-Ayoub; Kane Jacob; Laure Vendier; Michel Etienne; Eleuterio Álvarez; Ana Caballero; M. Mar Díaz-Requejo; Pedro J. Pérez
Journal of the American Chemical Society | 2003
Emmanuelle Despagnet-Ayoub; Stéphane Solé; Heinz Gornitzka; Alexander B. Rozhenko; Wolfgang W. Schoeller; Didier Bourissou; Guy Bertrand
Organometallics | 2013
Emmanuelle Despagnet-Ayoub; Lawrence M. Henling; Jay A. Labinger; John E. Bercaw
Organometallics | 2009
Emmanuelle Despagnet-Ayoub; Sophie Schigand; Laure Vendier; Michel Etienne
European Journal of Organic Chemistry | 2003
Emmanuelle Despagnet-Ayoub; Heinz Gornitzka; Didier Bourissou; Guy Bertrand