Strong C–H bond deactivation toward HAT has been observed in the reactions of the cumyloxyl radical with 1,2- and 1,3-diols, following addition of Li+ and Ca2+. Weaker effects have been observed with Mg2+. The role of the substrate structure and of the metal ion in the formation of Lewis acid–base complexes is discussed.

Martin, T., Salamone, M., Bietti, M. (2019). Hydrogen Atom Transfer from 1,2- and 1,3-Diols to the Cumyloxyl Radical. The Role of Structural Effects on Metal-Ion Induced C-H Bond Deactivation. CHEMICAL COMMUNICATIONS, 55, 5227-5230 [10.1039/c9cc01879d].

Hydrogen Atom Transfer from 1,2- and 1,3-Diols to the Cumyloxyl Radical. The Role of Structural Effects on Metal-Ion Induced C-H Bond Deactivation

Teo Martin
Membro del Collaboration Group
;
Michela Salamone
Membro del Collaboration Group
;
Massimo Bietti
2019-01-01

Abstract

Strong C–H bond deactivation toward HAT has been observed in the reactions of the cumyloxyl radical with 1,2- and 1,3-diols, following addition of Li+ and Ca2+. Weaker effects have been observed with Mg2+. The role of the substrate structure and of the metal ion in the formation of Lewis acid–base complexes is discussed.
2019
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/06 - CHIMICA ORGANICA
English
Con Impact Factor ISI
Martin, T., Salamone, M., Bietti, M. (2019). Hydrogen Atom Transfer from 1,2- and 1,3-Diols to the Cumyloxyl Radical. The Role of Structural Effects on Metal-Ion Induced C-H Bond Deactivation. CHEMICAL COMMUNICATIONS, 55, 5227-5230 [10.1039/c9cc01879d].
Martin, T; Salamone, M; Bietti, M
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/232202
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