Direct functionalization of C−H bonds by electrophilic anions

Significance Functionalization of unreactive molecules is a significant chemical challenge relevant to the conversion of abundant feedstocks such as alkanes into high-value chemicals. Herein, we demonstrate a new mechanism of alkane functionalization by the substitution of a proton by an anion in an alkyl chain. The reactive anion used for this reaction is generated from a highly stable precursor. The reaction mechanism is established using experimental and computational approaches, and the products are collected in the condensed phase using high-flux mass-selected ion deposition. This paves the way for exploiting the properties of gaseous ions for the generation of complex molecular structures in the condensed phase.