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Updated: Jan 21, 2026

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Gas-Phase Dehydrogenation of Alkanes: C-H Activation by a Graphene-Supported Nickel Single-Atom Catalyst Model
Michael Borrome1, Scott Gronert2
1Department of Chemistry, Virginia Commonwealth University, 1001 W. Main St., Richmond, VA, 23284, USA.
Abstract:
A gas-phase anionic nickel(0) fluorenyl complex is shown to effect the dehydrogenation of linear, branched, and cyclic alkanes via C-H activation. It performs dehydrogenations via a C-H insertion followed by β-hydride elimination. When given energy via collision-induced dissociation, the system is capable of second and third dehydrogenations to form dienes and aromatics such as benzene. Kinetic isotope effects and DFT calculations completed at the M06/6-311+G** level support the proposed mechanism. The metal complex can act as an experimental model for graphene-supported nickel single-atom catalysts and suggests that these catalysts are capable of alkane dehydrogenation via C-H activation.
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