Photocatalytic dihydroxylation of light olefins to glycols by water
Chunyang Dong,
Yinghao Wang,
Ziqi Deng,
Wenchao Wang,
Maya Marinova,
Karima Tayeb,
Jean-Charles Morin,
Melanie Dubois,
Martine Trentesaux,
Yury G. Kolyagin,
My Nghe Tran,
Vlad Martin-Diaconescu,
Olga Safonova,
Jeremie Zaffran,
Andrei Y. Khodakov () and
Vitaly V. Ordomsky ()
Additional contact information
Chunyang Dong: UMR
Yinghao Wang: UMR
Ziqi Deng: The University of Hong Kong
Wenchao Wang: Nanjing University of Science & Technology
Maya Marinova: FR
Karima Tayeb: F-
Jean-Charles Morin: UMR
Melanie Dubois: UMR
Martine Trentesaux: UMR
Yury G. Kolyagin: UMR
My Nghe Tran: UMR
Vlad Martin-Diaconescu: Carrer de la Llum 2-26
Olga Safonova: Paul Scherrer Institute
Jeremie Zaffran: UMI 3464 CNRS-Solvay
Andrei Y. Khodakov: UMR
Vitaly V. Ordomsky: UMR
Nature Communications, 2024, vol. 15, issue 1, 1-12
Abstract:
Abstract Aliphatic diols such as ethylene and propylene glycol are the key products in the chemical industry for manufacturing polymers. The synthesis of these molecules usually implies sequential processes, including epoxidation of olefins using hydrogen peroxide or oxygen with subsequent hydrolysis to glycols. Direct hydroxylation of olefins by cheap and green oxidants is an economically attractive and environmentally friendly route for the synthesis of diols. Here, we report a photocatalytic reaction for the dihydroxylation of ethylene and propylene to their glycols at room temperature using water as the oxidant. The photocatalyst contains Pd clusters stabilized by sub-nanometric polyoxometalate with TiO2 as the host material. Under light irradiation, it results in production rates of ethylene glycol and propylene glycols of 146.8 mmol·gPd−1·h−1 and 28.6 mmol·gPd−1·h−1 with liquid-phase selectivities of 63.3 % and 80.0 %, respectively. Meanwhile, green hydrogen derived from water is produced as another valuable product. Combined spectroscopy investigation suggests that the reaction proceeds via π-bonded adsorption of olefins over Pd clusters with hydroxylation by hydroxyl radicals formed by photocatalytic dissociation of water.
Date: 2024
References: View references in EconPapers View complete reference list from CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-024-52461-9 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52461-9
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-024-52461-9
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().