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Issue 2, 2016
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Mono- and tri-ester hydrogenolysis using tandem catalysis. Scope and mechanism

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Abstract

The scope and mechanism of thermodynamically leveraged ester RC(O)O–R′ bond hydrogenolysis by tandem metal triflate + supported Pd catalysts are investigated both experimentally and theoretically by DFT and energy span analysis. This catalytic system has a broad scope, with relative cleavage rates scaling as, tertiary > secondary > primary ester at 1 bar H2, yielding alkanes and carboxylic acids with high conversion and selectivity. Benzylic and allylic esters display the highest activity. The rate law is ν = k[M(OTf)n]1[ester]0[H2]0 with an H/D kinetic isotope effect = 6.5 ± 0.5, implying turnover-limiting C–H scission following C–O cleavage, in agreement with theory. Intermediate alkene products are then rapidly hydrogenated. Applying this approach with the very active Hf(OTf)4 catalyst to bio-derived triglycerides affords near-quantitative yields of C3 hydrocarbons rather than glycerol. From model substrates, it is found that RC(O)O–R′ cleavage rates are very sensitive to steric congestion and metal triflate identity. For triglycerides, primary/external glyceryl CH2–O cleavage predominates over secondary/internal CH–O cleavage, with the latter favored by less acidic or smaller ionic radius metal triflates, raising the diester selectivity to as high as 48% with Ce(OTf)3.

Graphical abstract: Mono- and tri-ester hydrogenolysis using tandem catalysis. Scope and mechanism

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The article was received on 23 Oct 2015, accepted on 26 Nov 2015 and first published on 26 Nov 2015


Article type: Paper
DOI: 10.1039/C5EE03256C
Author version available: Download Author version (PDF)
Citation: Energy Environ. Sci., 2016,9, 550-564
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    Mono- and tri-ester hydrogenolysis using tandem catalysis. Scope and mechanism

    T. L. Lohr, Z. Li, R. S. Assary, L. A. Curtiss and T. J. Marks, Energy Environ. Sci., 2016, 9, 550
    DOI: 10.1039/C5EE03256C

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