Peralkylated imidazolium carbonate ionic liquids: synthesis using dimethyl carbonate, reactivity and structure

Content Provider	Semantic Scholar
Author	Maton, Cedric Hecke, Kristof Van Stevens, Christian V.
Copyright Year	2015
Abstract	Tri- and tetra-alkylimidazoles are quaternised into their corresponding ionic liquids with dimethyl carbonate. Upon metathesis of the obtained methyl carbonate salts, only gaseous by-products are generated. These methyl carbonate salts can be transformed into hydrogen carbonate salts by reaction with water. The salts containing a carbonate anion are very alkaline, which results in a hydrogen/deuterium exchange on the anion and some of the cation protons, depending on the substitution. Moreover, the crystalline 1-ethyl-3,4,5-trimethylimidazolium hydrogen carbonate formed carboxylate species upon dissolution. In particular, the carboxylate was able to regenerate the carbene and in the presence of chloroform, this led to the formation of the chloride salt.
Starting Page	461
Ending Page	468
Page Count	8
File Format	PDF HTM / HTML
DOI	10.1039/C4NJ01301H
Alternate Webpage(s)	https://pubs.rsc.org/en/content/getauthorversionpdf/C4NJ01301H
Alternate Webpage(s)	https://doi.org/10.1039/C4NJ01301H
Volume Number	39
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article