Main-group compounds selectively activate natural gas alkanes under room temperature and atmospheric pressure

Abstract

Most C–H bond activations of natural gas alkanes rely on transition metal complexes. Activations by using main-group systems have been reported but required heating or photo-irradiation under high atmospheric pressure with rather low regioselectivity. Here we report that Lewis acid-carbene adducts facilely undergo oxidative additions to C–H bonds of ethane, propane and n-butane with high selectivity under room temperature and atmospheric pressure. The Lewis acids can be moved by the addition of a base and the carbene-derived products can be easily converted into aldehydes. This work offers a route for main-group element compounds to selectively functionalise C–H bonds of natural gas alkanes and other small molecules. Activation of natural gas alkanes using main-group systems typically requires heating or photo-irradiation under high atmospheric pressure with low regioselectivity. Here the authors report Lewis acid-carbene adduct activation of C–H bonds in ethane, propane and n-butane under one atmospheric pressure and at room temperature with high selectivity.