Banerjee Sayak, Rodriguez Jessica, Mais Marco, Perras Frédéric A, Sadow Aaron D
Department of Chemistry, Iowa State University, Ames, IA, 50011, United States.
Ames National Laboratory, Iowa State University, Ames, IA, 50011, United States.
Angew Chem Int Ed Engl. 2025 Sep 1;64(36):e202511893. doi: 10.1002/anie.202511893. Epub 2025 Jul 30.
Surface grafted organozirconium catalyzes C─H/Et─Al exchange reactions, involving saturated hydrocarbons and AlEt, to afford organoaluminum compounds and ethane. The Zr(OBu)@SiO-AlO (1) catalyst contains monopodal ≡SiO─Zr(OBu) 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 ─SiMe. Residual silanols in 1 react with allyltrimethylsilane, as determined by solid-state C and Si nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and reaction stoichiometry, to form Zr(OBu)/SiMe@SiO-AlO (2), which is resistant to degradation by AlEt. 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 AlMe.
表面接枝的有机锆催化涉及饱和烃和三乙基铝的C─H/乙基铝交换反应,生成有机铝化合物和乙烷。Zr(OBu)@SiO-AlO (1)催化剂含有单足≡SiO─Zr(OBu)且仅含少量残余硅醇(<5%)。然而,这些硅醇是1的致命弱点,在催化过程中为表面和催化剂降解提供了一条途径,限制了烷基铝的产率和催化剂的周转率。通过用─SiMe封端硅醇可抑制涉及活性表面有机金属化合物对Si─O键的裂解的载体降解。通过固态碳和硅核磁共振(NMR)光谱、红外(IR)光谱和反应化学计量学确定,1中的残余硅醇与烯丙基三甲基硅烷反应,形成Zr(OBu)/SiMe@SiO-AlO (2),其对三乙基铝的降解具有抗性。与1相比,由2催化的十二烷的C─H铝化反应产生更高产率的1-十二烷基铝产物,且选择性>95%。此外,甲烷发生由2催化的C─H铝化反应,提供了一条制备甲基铝的途径。