M
Matthew S. Ide
Researcher at ExxonMobil
Publications - 35
Citations - 1176
Matthew S. Ide is an academic researcher from ExxonMobil. The author has contributed to research in topics: Catalysis & Alcohol oxidation. The author has an hindex of 9, co-authored 31 publications receiving 1013 citations. Previous affiliations of Matthew S. Ide include University of Virginia.
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Selective oxidation of alcohols and aldehydes over supported metal nanoparticles
TL;DR: In this article, the authors examined the literature on supported metal catalysts for the oxidation of molecules of interest in biomass conversion (primary alcohols, polyols, 5-hydroxymethylfurfural, and various sugars).
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Mechanistic insights on the hydrogenation of α,β-unsaturated ketones and aldehydes to unsaturated alcohols over metal catalysts
TL;DR: In this paper, the selective hydrogenation of unsaturated ketones (methyl vinyl ketone and benzalacetone) and unsaturated aldehydes (crotonaldehyde and cinnamaldehyde) was carried out with H2 at 2 bar absolute over Pd/C, Pt/C and Ru/C catalysts in ethanol or water solvent at 333 K.
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The important role of hydroxyl on oxidation catalysis by gold nanoparticles.
Matthew S. Ide,Robert J. Davis +1 more
TL;DR: The important role of hydroxyl for these two oxidation reactions catalyzed by gold, in terms of its influence on the turnover frequency is discussed, and the use of water as a "green" solvent becomes an attractive choice.
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On the deactivation of supported platinum catalysts for selective oxidation of alcohols
TL;DR: In this article, the oxidation of a variety of terminal alcohols with O2 in liquid water at 343 K over Pt supported on C, BN, SiO2, TiO2 and Al2O3 was explored to determine the origin of catalyst deactivation.
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Perspectives on the kinetics of diol oxidation over supported platinum catalysts in aqueous solution
Matthew S. Ide,Robert J. Davis +1 more
TL;DR: In this paper, the catalytic oxidation of a variety of terminal alcohols was performed over Pt/C with 10 bar dioxygen at 343 K in aqueous solvent at low pH.