Elucidating Dramatic Ligand Effects on SET Processes: Iron Hydride versus Iron Borohydride Catalyzed Reductive Radical Cyclization of Unsaturated Organic Halides

Abstract : An iron(II) borohydride complex ([(η1-H3BH)FeCl(NCCH3)4]) is employed as the precatalyst in iron-catalyzed radical cyclizations of unsaturated organic halides in the presence of NaBH4. Mechanistic investigations have established that the ligand bound to the metal center (acetonitrile versus ethylenebis(diphenylphosphine) (dppe)) plays a crucial role in the structure and reactivity of the active anionic iron(I) hydride ([HFeCl(dppe)2]−) and borohydride ([(η1-H3BH)FeCl(NCCH3)4]−) with unsaturated haloacetals. This work provides new insights into iron(I) hydride and borohydride species and their potential implication in single-electron processes.
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Organometallics, American Chemical Society, 2018, 37 (5 S.I), pp.761-771. 〈10.1021/acs.organomet.7b00603〉
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https://hal.archives-ouvertes.fr/hal-01787576
Contributeur : Nathalie Gon <>
Soumis le : lundi 7 mai 2018 - 16:21:08
Dernière modification le : mercredi 9 mai 2018 - 01:15:25

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Sara H. Kyne, Martin Clemancey, Geneviève Blondin, Etienne Derat, Louis Fensterbank, et al.. Elucidating Dramatic Ligand Effects on SET Processes: Iron Hydride versus Iron Borohydride Catalyzed Reductive Radical Cyclization of Unsaturated Organic Halides. Organometallics, American Chemical Society, 2018, 37 (5 S.I), pp.761-771. 〈10.1021/acs.organomet.7b00603〉. 〈hal-01787576〉

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