Surface Protected Organozirconium Catalyzes C─H Alumination of Saturated Hydrocarbons
Aaron David Sadow1,2, Sayak Banerjee2, Jessica Rodriguez2
1Department of Chemistry, Iowa State University, Ames, IA, 50011, United States.
Abstract:
Surface grafted organozirconium catalyzes C─H/Et─Al exchange reactions, involving saturated hydrocarbons and AlEt3, to afford organoaluminum compounds and ethane. The Zr(OtBu)3@SiO2-Al2O3-700 (1) catalyst contains monopodal ≡SiO─Zr(OtBu)3 and only a few residual silanols (<5%). Nonetheless, these silanols are the Achille's heel of 1, providing a pathway for surface and catalyst degradation during catalysis, limiting the alkylaluminum yield and catalyst turnover. Support degradation, involving the cleavage of Si─O bonds by activated surface organometallics, is inhibited by capping silanols with ─SiMe3. Residual silanols in 1 react with allyltrimethylsilane, as determined by solid-state 13C and 29Si nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and reaction stoichiometry, to form Zr(OtBu)3/SiMe3@SiO2-Al2O3-700 (2), which is resistant to degradation by AlEt3. C─H alumination of dodecane catalyzed by 2 produces higher yields of the 1-dodecylaluminum product in comparison to 1, and in >95% selectivity. Additionally, methane undergoes 2-catalyzed C─H alumination, providing a route to AlMe3.
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