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

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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… Click to show full 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 λ = 180-254 nm, the enols rearrange to the simplest sugar glycolaldehyde.

Keywords: ethenediol glycolaldehyde; isolation photorearrangement; photorearrangement cis; matrix isolation; trans ethenediol; cis trans

Journal Title: Chemical communications
Year Published: 2023

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