Novel Lewis-base ionic liquids replacing typical anions


Autoria(s): Yoshizawa-Fujita, Masahiro; Johansson, Katarina; Newman, Peter; MacFarlane, Douglas R.; Forsyth, Maria
Data(s)

17/04/2006

Resumo

We have synthesized two kinds of new Lewis-base ionic liquids (ILs); one is based on the relatively strong Lewis basic acetate anion, and the other is a salt composed of a mono-alkylated diamine such that the Lewis base site is incorporated in the cation. 1-Octyl-4-aza-1-azonia-bicyclo[2.2.2]octane bis(trifluoromethanesulfonyl)amide, [C<sub>8</sub>dabco]TFSA, and <i>N</i>-butyl-<i>N</i>-methylpyrrolidinium acetate, [p<sub>1,4</sub>]OAc, melted into fluid liquids at 26 and 81 °C, respectively. The thermal decomposition of [p<sub>1,4</sub>]OAc started at around 150 °C, whereas the thermal stability of [C<sub>8</sub>dabco]TFSA was almost equal to that of typical TFSA-based ILs in spite of the Lewis base site. This suggests that if the Lewis base site is incorporated into the cation the IL can maintain higher thermal stability. In addition, as a further result of the presence of the basic nitrogen, [C<sub>8</sub>dabco]TFSA can dissolve hydrated Cu(NO<sub>3</sub>)<sub>2</sub> whereas the other TFSA-based ILs cannot.<br />

Identificador

http://hdl.handle.net/10536/DRO/DU:30030297

Idioma(s)

eng

Publicador

Elsevier

Relação

http://dro.deakin.edu.au/eserv/DU:30030297/forsyth-novellewisbase-2006.pdf

http://dx.doi.org/10.1016/j.tetlet.2006.02.073

Direitos

2006, Elsevier Ltd.

Palavras-Chave #ionic liquids #Lewis base #nucleophilicity #pyrrolidinium salts
Tipo

Journal Article