Effects of Chain Length on the Mechanism and Rates of Metal-Catalyzed Hydrogenolysis of n-Alkanes

David D. Hibbitts, David W. Flaherty, Enrique Iglesia

Research output: Contribution to journalArticle

Abstract

C-C cleavage in C2-C10 n-alkanes involves quasi-equilibrated C-H activation steps to form dehydrogenated intermediates on surfaces saturated with H atoms. These reactions are inhibited by H2 to similar extents for C-C bonds of similar substitution in all acyclic and cyclic alkanes and, thus, show similar kinetic dependences on H2 pressure. Yet, turnover rates depend sensitively on chain length because of differences in activation enthalpies (ΔH) and entropies (ΔS) whose mechanistic origins remain unclear. Density functional theory (DFT) estimates of ΔH and ΔG for C-C cleavage via >150 plausible elementary steps for propane and n-butane reactants on Ir show that hydrogenolysis occurs via α,β-bound RC∗-C∗R′ transition states (R = H, CxH2x+1) in which two H atoms are removed from each C∗. Calculated ΔH values decrease with increasing alkane chain length (C2-C8), consistent with experiment, because attractive van der Waals interactions with surfaces preferentially stabilize larger transition states. A concomitant increase in ΔS, evident from experiments, is not captured by periodic DFT methods, which treat low-frequency vibrational modes inaccurately, but statistical mechanics treatments describe such effects well for RC∗-C∗R species, as previously reported. These findings, together with parallel studies of the cleavage of more substituted C-C bonds in branched and cyclic alkanes, account for the reasons that chain length and substitution influence ΔH and ΔS values and the dependence of rates on H2 pressure and consequently explain differences in hydrogenolysis reactivities and selectivities across all alkanes.

Original languageEnglish (US)
Pages (from-to)8125-8138
Number of pages14
JournalJournal of Physical Chemistry C
Volume120
Issue number15
DOIs
StatePublished - May 5 2016

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Energy(all)
  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films

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