CO2 utilization in a micellar system: synthesis of cyclic carbonates

14 October 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Fixation of carbon dioxide from its waste streams into value added products, in organic synthesis processes, whilst challenging, would lead to great ecological benefits. To this end, a CO2 cycloaddition to epoxides seems most promising as it is a 100% atom economic reaction leading to valuable cyclic carbonates. However, many of the reaction systems utilized for their synthesis employ organic solvents, high temperatures, and high pressure. Thus, the micellar conditions reported here achieve a metal and organic solvent free approach, giving access to not only carbonates but also carbamates without the need for pressurization or heating. Extensive studies of interactions between micelles and carbon dioxide opens up pathways to use this gaseous reagent in aqueous media.

Keywords

Carbon dioxide
micelles
micellar catalysis
surfactants
cyclic carbonates
carbon disulfide
epoxides
aziridines
carbamates

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.