<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Xie S</submitter><pubmed_abstract>The development of new methods for the direct transformation of methanol into two or multi-carbon compounds via controlled carbon-carbon coupling is a highly attractive but challenging goal. Here, we report the first visible-light-driven dehydrogenative coupling of methanol into ethylene glycol, an important chemical currently produced from petroleum. Ethylene glycol is formed with 90% selectivity and high efficiency, together with hydrogen over a molybdenum disulfide nanofoam-modified cadmium sulfide nanorod catalyst. Mechanistic studies reveal a preferential activation of C-H bond instead of O-H bond in methanol by photoexcited holes on CdS via a concerted proton-electron transfer mechanism, forming a hydroxymethyl radical (⋅CH2OH) that can readily desorb from catalyst surfaces for subse</pubmed_abstract><journal>Nature communications</journal><pagination>1181</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5862904</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Visible light-driven C-H activation and C-C coupling of methanol into ethylene glycol.</pubmed_title><pmcid>PMC5862904</pmcid><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Deng D</pubmed_authors><pubmed_authors>Shen Z</pubmed_authors><pubmed_authors>Ma C</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Deng J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Xie S</pubmed_authors><pubmed_authors>Guo P</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Cheng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Visible light-driven C-H activation and C-C coupling of methanol into ethylene glycol.</name><description>The development of new methods for the direct transformation of methanol into two or multi-carbon compounds via controlled carbon-carbon coupling is a highly attractive but challenging goal. Here, we report the first visible-light-driven dehydrogenative coupling of methanol into ethylene glycol, an important chemical currently produced from petroleum. Ethylene glycol is formed with 90% selectivity and high efficiency, together with hydrogen over a molybdenum disulfide nanofoam-modified cadmium sulfide nanorod catalyst. Mechanistic studies reveal a preferential activation of C-H bond instead of O-H bond in methanol by photoexcited holes on CdS via a concerted proton-electron transfer mechanism, forming a hydroxymethyl radical (⋅CH2OH) that can readily desorb from catalyst surfaces for subse</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-19T15:19:36.727Z</modification><creation>2019-03-26T23:20:35Z</creation></dates><accession>S-EPMC5862904</accession><cross_references><pubmed>29563511</pubmed><doi>10.1038/s41467-018-03543-y</doi></cross_references></HashMap>