When Chlorides are the Most Reactive: A Simple Route towards Diverse Mono- and Dicationic Dimethyl Phosphate Ionic Liquids

Elina Priede (Corresponding Author), Eduards Baķis, Andris Zicmanis

Research output: Contribution to journalLetterpeer-review

8 Citations (Scopus)

Abstract

Structurally diverse aromatic and aliphatic ionic liquids have been prepared via anion metathesis utilizing alkylammonium chlorides and trimethyl phosphate. Excellent oxygen-containing functional-group tolerance in preparation of potentially greener dimethyl phosphate ionic liquids has been demonstrated. For the first time, this method has been employed in the synthesis of dicationic imidazolium-based ionic liquids possessing a dimethyl phosphate counterion, providing a simple, direct route towards structurally novel products of high purity.

Original languageEnglish
Article numberst-2014-d0499-l
Pages (from-to)2447-2450
Number of pages4
JournalSynlett
Volume25
Issue number17
DOIs
Publication statusPublished - 22 Oct 2014
Externally publishedYes

Keywords*

  • anion metathesis
  • dicationic ionic liquids
  • dimethyl phosphate
  • monocationic ionic liquids

Field of Science*

  • 1.4 Chemical sciences

Publication Type*

  • 1.1. Scientific article indexed in Web of Science and/or Scopus database

Fingerprint

Dive into the research topics of 'When Chlorides are the Most Reactive: A Simple Route towards Diverse Mono- and Dicationic Dimethyl Phosphate Ionic Liquids'. Together they form a unique fingerprint.

Cite this