Journal article

Matrix isolation and photorearrangement of cis- and trans-1,2-ethenediol to glycolaldehyde


Authors listMardyukov, A; Wende, RC; Schreiner, PR

Publication year2023

Pages2596-2599

JournalChemical Communications

Volume number59

Issue number18

ISSN1359-7345

eISSN1364-548X

Open access statusGreen

DOI Linkhttps://doi.org/10.1039/d2cc06331j

PublisherRoyal Society of Chemistry


Abstract
1,2-Ethenediols are deemed key intermediates in prebiotic and interstellar syntheses of carbohydrates. Here we present the gas-phase synthesis of these enediols, the high-energy tautomers of glycolaldehyde, trapped in cryogenic argon matrices. Importantly, upon photolysis at lambda = 180-254 nm, the enols rearrange to the simplest sugar glycolaldehyde.



Citation Styles

Harvard Citation styleMardyukov, A., Wende, R. and Schreiner, P. (2023) Matrix isolation and photorearrangement of cis- and trans-1,2-ethenediol to glycolaldehyde, Chemical Communications, 59(18), pp. 2596-2599. https://doi.org/10.1039/d2cc06331j

APA Citation styleMardyukov, A., Wende, R., & Schreiner, P. (2023). Matrix isolation and photorearrangement of cis- and trans-1,2-ethenediol to glycolaldehyde. Chemical Communications. 59(18), 2596-2599. https://doi.org/10.1039/d2cc06331j


Last updated on 2025-10-06 at 11:49