Journal article

A Two-Step Catalytic Cycle for the Acceptorless Dehydrogenation of Ethane by Group 10 Metal Complexes: Role of the Metal in Reactivity and Selectivity

Kevin Parker, Geethika K Weragoda, Allan J Canty, Anastasios Polyzos, Victor Ryzhov, Richard AJ O'Hair

Organometallics | American Chemical Society | Published : 2020

Abstract

Acceptorless dehydrogenation of ethane was achieved in the gas phase via a two-step catalytic cycle involving ternary cationic metal hydrides, [(phen)M(H)]+, 1, and metal ethides, [(phen)M(CH2CH3)]+, 2, (where M = Ni, Pd, or Pt, and phen = 1,10-phenanthroline). Species 1 and 2 were generated and their reactivity studied in a quadrupole ion trap mass spectrometer. It was found that 1 readily reacted with ethane releasing H2 and forming 2, with the relative reactivity being Pt > Ni ≫ Pd. Density functional theory (DFT) calculations for this metathesis reaction agree with the experimental reactivity order. Species 2 can in turn be converted into 1 and release ethylene when sufficient energy is ..

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University of Melbourne Researchers

Grants

Awarded by ARC


Awarded by American Chemical Society Petroleum Research Fund


Awarded by NSF MRI program


Funding Acknowledgements

We acknowledge the support of the ARC (DP180101187 funding to A.J.C. and RAJO), and the National Computing Infrastructure. We also acknowledge the generous support from the Donors of the American Chemical Society Petroleum Research Fund (PRF #59763-ND6 to V.R.) for partial support of this research as well as the NSF MRI program (award #CHE:1726931 to V.R.) for the purchase of the high-resolution mass spectrometer.