On the catalytic activity of [RuH2(PPh3)3(CO)] (PPh3 = triphenylphosphine) in ruthenium-catalysed generation of hydrogen from alcohol : a combined experimental and DFT study
Abstract
Using Density Functional Theory calculations (at the B97-D2//BP86 level) and measurements of kinetic isotope effects, we explored the mechanism of [RuH2(PPh3)3(CO)] ( 22 ) in catalytic acceptor-less dehydrogenation of methanol to formaldehyde. 22 is found to exhibit a similar activity as the previously studied [RuH2(H2)(PPh3)3] ( 1b ) complex. On the computed pathway, η2 → η1 slippage of Ru-bound formaldehyde prior to decoordination is indicated to be rate-limiting, consistent with the low kH/kD KIE of 1.3 measured for this reaction. We also explored computationally the possibility of achieving complete dehydrogenation of methanol (into CO2 and H2), through subsequent decarbonylation of formaldehyde and water-gas shift reaction of the resulting carbonyl complex. Complete pathways of this kind are traced for 22 and for [RuH2(PPh3)2(CO)2]. An alternative mechanism, involving a gem-diol intermediate (obtained upon attack of OH- to coordinated formaldehyde), has also been investigated. All these pathways turned out to be unfavourable kinetically, in keeping with the lack of CO2 evolution experimentally observed in this system. Our calculations show that the reactions are hampered by the low electrophilicities of the CO and HCHO ligands, making OH- uptake unfavourable. Consequently, the subsequent intermediates are too high-lying on the reaction profiles, thus leading to high kinetic barriers and preventing full dehydrogenation of methanol to occur by this kind of mechanism.
Citation
Lorusso , P , Ahmad , S , Brill , K , Cole-Hamilton , D J , Sieffert , N & Buehl , M 2020 , ' On the catalytic activity of [RuH 2 (PPh 3 )3(CO)] (PPh 3 = triphenylphosphine) in ruthenium-catalysed generation of hydrogen from alcohol : a combined experimental and DFT study ' , ChemCatChem , vol. Early View . https://doi.org/10.1002/cctc.202000159
Publication
ChemCatChem
Status
Peer reviewed
ISSN
1867-3880Type
Journal article
Description
We wish to thank Lucite International for a studentship (P.L.) and EaStCHEM for support and access to the EaStCHEM Research Facility. We also thank Dr. H. Früchtl for technical support. N.S. thanks the Univ. Grenoble Alpes, the CNRS and the ICMG FR 2607 for financial support. The Pcecic and Froggy platforms of the CIMENT infrastructure are also acknowledged (project “liqsim”).Collections
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