Partnering a Three-Coordinate Gallium Cation with a Hydroborate Counter-Ion for the Catalytic Hydrosilylation of CO2.

Abstract

A novel β-diketiminate stabilized gallium hydride, (Dipp L)Ga(Ad)H (where (Dipp L)={HC(MeCDippN)2 }, Dipp=2,6-diisopropylphenyl and Ad=1-adamantyl), has been synthesized and shown to undergo insertion of carbon dioxide into the Ga-H bond under mild conditions. In this case, treatment of the resulting κ1 -formate complex with triethylsilane does not lead to regeneration of the hydride precursor. However, when combined with B(C6 F5 )3 , (Dipp L)Ga(Ad)H catalyses the reductive hydrosilylation of CO2 . Under stoichiometric conditions, the addition of one equivalent of B(C6 F5 )3 to (Dipp L)Ga(Ad)H leads to the formation of a 3-coordinate cationic gallane complex, partnered with a hydroborate anion, [(Dipp L)Ga(Ad)][HB(C6 F5 )3 ]. This complex rapidly hydrometallates carbon dioxide and catalyses the selective reduction of CO2 to the formaldehyde oxidation level at 60 °C in the presence of Et3 SiH (yielding H2 C(OSiEt3 )2 ). When catalysis is undertaken in the presence of excess B(C6 F5 )3 , appreciable enhancement of activity is observed, with a corresponding reduction in selectivity: the product distribution includes H2 C(OSiEt3 )2 , CH4 and O(SiEt3 )2 . While this system represents proof-of-concept in CO2 hydrosilylation by a gallium hydride system, the TOF values obtained are relatively modest (max. 10 h-1 ). This is attributed to the strength of binding of the formatoborate anion to the gallium centre in the catalytic intermediate (Dipp L)Ga(Ad){OC(H)OB(C6 F5 )3 }, and the correspondingly slow rate of the turnover-limiting hydrosilylation step. In turn, this strength of binding can be related to the relatively high Lewis acidity measured for the [(Dipp L)Ga(Ad)]+ cation (AN=69.8).