DFT study on mechanism of carbonyl hydrosilylation catalyzed by high-valent molybdenum (IV) hydrides. Issue 29 (19th July 2018)

• Record Type: Journal Article
• Authors: Chen, Hongcai; Wang, Wenmin; Wei, Haiyan
• Is Part Of: Tetrahedron. Volume 74:Issue 29(2018)
• Page Start: 3955
• Page End: 3962
• Publication Date: 2018-07-19
• Subjects: Hydrosilylation -- Ionic hydrosilylation pathway -- Carbonyl insertion pathway -- DFT -- Molybdenum hydride; Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1016/j.tet.2018.05.078
• Languages: English
• ISSNs: 0040-4020

Abstract

Abstract: Density functional theory (DFT) calculations have been employed to investigate hydrosilylation of carbonyl compounds catalyzed by three high-valent molybdenum (VI) hydrides: Mo(NAr)H(Cp)(PMe3 ) (1A ), Mo(NAr)H(PMe3 )3 (1B ), and Mo(NAr)H (Tp)(PMe3 ) (Tp = tris(pyrazolyl) borate) (1C ). Three independent mechanisms have been explored. The first mechanism is "carbonyl insertion pathway", in which the carbonyls insert into Mo−H bond to give a metal alkoxide complex. The second mechanism is the "ionic hydrosilylation pathway", in which the carbonyls nucleophilically attacks η 1 -silane molybdenum adduct. The third mechanism is [2 + 2] addition mechanism which was proposed to be favorable for the high-valent di-oxo molybdenum complex MoO2 Cl2 catalyzing the hydrosilylation. Our studies have identified the "carbonyl insertion pathway" to be the preferable pathway for three molybdenum hydrides catalyzing hydrosilylation of carbonyls. For Mo(NAr)H (Tp)(PMe3 ) (Tp = tris(pyrazolyl) borate), the proposed nonhydride mechanism experimentally is calculated to be more than 32.6 kcal/mol higher than the "carbonyl insertion pathway". Our calculation results have derived meaningful mechanistic insights for the high-valent transition metal complexes catalyzing the reduction reaction. Graphical abstract: Image 1