Evidence map›Paper›PMID 39294117›Full record

ArticleNature communications2024

Photocatalytic dihydroxylation of light olefins to glycols by water.

Chunyang Dong, Yinghao Wang, Ziqi Deng, Wenchao Wang, Maya Marinova, Karima Ben Tayeb, Jean-Charles Morin, Melanie Dubois, Martine Trentesaux, Yury G Kolyagin and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Chunyang Dong *UCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France.
Yinghao Wang *UCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France.
Ziqi DengDepartment of Chemistry, The University of Hong Kong, Hong Kong, China.
Wenchao WangSchool of New Energy, Nanjing University of Science & Technology, Jiangyin, 214443, China.
Maya MarinovaUMET-Institut Michel-Eugène Chevreul, Université de Lille, CNRS, INRAE, Centrale Lille, Université d'Artois, FR, 2638, Lille, France.
Karima Ben TayebUniversité de Lille, CNRS, UMR 8516 - LASIRE - Laboratoire de Spectroscopie pour les Interactions, la Réactivité et l'Environnement, F-, 59000, Lille, France.ORCID http://orcid.org/0000-0002-4595-4225
Jean-Charles MorinUCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France.
Melanie DuboisUCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France.
Martine TrentesauxUCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France.
Yury G KolyaginUCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France.ORCID http://orcid.org/0000-0001-8095-6923
My Nghe TranUCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France.
Vlad Martin-DiaconescuALBA Synchrotron - CELLS, Carrer de la Llum 2-26, 08290, Cerdanyola del Vallès Barcelona, Spain.
Olga SafonovaPaul Scherrer Institute, 5232, Villigen, Switzerland.ORCID http://orcid.org/0000-0002-6772-1414
Jeremie ZaffranEco-Efficient Products and Processes Laboratory (E2P2L), UMI 3464 CNRS-Solvay, Shanghai, China.
Andrei Y KhodakovUCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France. Andrei.Khodakov@univ-lille.fr.ORCID http://orcid.org/0000-0003-4599-3969
Vitaly V OrdomskyUCCS-Unité de Catalyse et Chimie du Solide, Université de Lille, CNRS, Centrale Lille, ENSCL, Université d'Artois, UMR, 8181, Lille, France. Vitaly.Ordomsky@univ-lille.fr.ORCID http://orcid.org/0000-0002-4814-5052

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-20-SODR-0002
6 · The paper itself

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 TiO

Identifiers

PMID39294117
PMCPMC11410969

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.