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Mercedes Boronat

Researcher at Polytechnic University of Valencia

Publications -  43
Citations -  3614

Mercedes Boronat is an academic researcher from Polytechnic University of Valencia. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 23, co-authored 32 publications receiving 3012 citations. Previous affiliations of Mercedes Boronat include Spanish National Research Council.

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Exceptional oxidation activity with size-controlled supported gold clusters of low atomicity

TL;DR: An easy method is reported to prepare isolated gold atoms supported on functionalized carbon nanotubes and their performance in the oxidation of thiophenol with O2, showing that single gold atoms are not active, but they aggregate under reaction conditions into gold clusters of low atomicity that exhibit a catalytic activity comparable to that of sulfhydryl oxidase enzymes.
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Determination of the catalytically active oxidation Lewis acid sites in Sn-beta zeolites, and their optimisation by the combination of theoretical and experimental studies

TL;DR: In this paper, two types of Lewis acid sites are shown to exist in Sn-beta zeolite: partially hydrolysed framework tin centers (Si O ) 3 Sn OH (sites A) and fully framework coordinated tin atoms Sn( Si O ) 4 (sites B).
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Accelerated crystallization of zeolites via hydroxyl free radicals

TL;DR: The formation of hydroxyl radicals, either by irradiation with ultraviolet light or with the Fenton reagent, can speed up the formation of the crystallized zeolite by about a factor of 2.Radically faster synthesis Zeolite synthesis normally proceeds under basic conditions that allow the oxide bridges between aluminum and silicon atoms to break and reform.
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Enzyme-like specificity in zeolites: a unique site position in mordenite for selective carbonylation of methanol and dimethyl ether with CO.

TL;DR: It is shown that when methanol carbonylation competes with hydrocarbon formation, the first reaction occurs preferentially within 8MR channels, and that only the T3-O33 positions are selective and that this selectivity is due to the unusual orientation of the methoxy group in relation to the 8MR channel.
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The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry.

TL;DR: A heterogeneous catalyst consisting of Pd4 clusters with mixed-valence 0/+1 oxidation states, stabilized and homogeneously organized within the walls of a metal-organic framework (MOF) outperforms state-of-the-art metal catalysts in carbene-mediated reactions of diazoacetates, with high yields and turnover numbers.