N-Methyl-N-Alkylpyrrolidinium Bis(perfluoroethylsulfonyl)amide ([NPf2]–) and Tris(trifluoromethanesulfonyl)methide ([CTf3]–) Salts: Synthesis and Characterization
Katarina M. Johansson A C , Josefina Adebahr B , Patrick C. Howlett B , Maria Forsyth B and Douglas R. MacFarlane AA School of Chemistry, Monash University, Clayton VIC 3800, Australia.
B Department of Materials Engineering, Monash University, Clayton VIC 3800, Australia.
C Corresponding author. Email: katarina.johansson@sci.monash.edu.au
Australian Journal of Chemistry 60(1) 57-63 https://doi.org/10.1071/CH06299
Submitted: 17 August 2006 Accepted: 12 October 2006 Published: 29 January 2007
Abstract
Novel salts based the pyrrolidinium cation [Cnmpyr]+ (where n denote the number of carbons in the straight alkyl chain) and either the [NPf2]– or [CTf3]– anions have been synthesized and characterized to determine their thermal behaviour, stability, and conductivity. [C1mpyr][NPf2], [C2mpyr][NPf2], and [C1mpyr][CTf3] exhibit behaviour indicative of a plastic crystal phase. Both [C3mpyr][NPf2] and [C4mpyr][NPf2] are RTILs, while all of the [CTf3]– salts, have melting points above 60°C. [C3mpyr][NPf2] exhibited the widest electrochemical window of 5.5 V. The [NPf2]– salt exhibited similar reductive limits to the [NTf2]– anion, –3.2 V versus Fc+|Fc, while [CTf3]– had lower reductive stability. The [CTf3]– salts were more stable towards oxidation, +2.5 V versus Fc+|Fc, compared to the [NPf2]– and [NTf2]– salts.
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unpublished.
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A This compound is frequently described as an ‘imide’ in the materials literature but more accurately, and consistently with related compounds, as an ‘amide’ in the chemical literature.