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Issue 1, 2018
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Ring hydrogenation of aromatic compounds in aqueous suspensions of an Rh-loaded TiO2 photocatalyst without use of H2 gas

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Abstract

There are various possibilities of co-catalyst-assisted photocatalytic reduction (CPR) over a titanium(IV) oxide (TiO2) photocatalyst, especially H2-free and chemoselective CPR. We examined the photoinduced ring hydrogenation of aromatics having a carboxyl group over metal-loaded TiO2 under H2-free conditions and found that the aromatics were almost quantitatively hydrogenated to the corresponding cyclohexanes having a carboxyl group when rhodium, water and oxalic acid were used as a metal co-catalyst, solvent and hole scavenger, respectively. The effects of different metal co-catalysts, solvents and hole scavengers on the ring hydrogenation were also examined. Based on the results obtained under various conditions, the light dependency and adsorption behavior of the aromatics and hole scavengers, the functions of TiO2 and the co-catalyst, and the reaction process are discussed.

Graphical abstract: Ring hydrogenation of aromatic compounds in aqueous suspensions of an Rh-loaded TiO2 photocatalyst without use of H2 gas

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Supplementary files

Article information


Submitted
20 Sep 2017
Accepted
13 Nov 2017
First published
13 Nov 2017

Catal. Sci. Technol., 2018,8, 139-146
Article type
Paper

Ring hydrogenation of aromatic compounds in aqueous suspensions of an Rh-loaded TiO2 photocatalyst without use of H2 gas

K. Nakanishi, R. Yagi, K. Imamura, A. Tanaka, K. Hashimoto and H. Kominami, Catal. Sci. Technol., 2018, 8, 139
DOI: 10.1039/C7CY01929G

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