Physical trends and structural features in organic salts of the thiocyanate anion

Pringle, Jennifer M., Golding, Jake, Forsyth, Craig M., Deacon, Glen B., Forsyth, Maria and MacFarlane, Douglas R. 2002, Physical trends and structural features in organic salts of the thiocyanate anion, Journal of materials chemistry, vol. 12, no. 12, pp. 3475-3480.

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Title Physical trends and structural features in organic salts of the thiocyanate anion
Author(s) Pringle, Jennifer M.
Golding, Jake
Forsyth, Craig M.
Deacon, Glen B.
Forsyth, Maria
MacFarlane, Douglas R.
Journal name Journal of materials chemistry
Volume number 12
Issue number 12
Start page 3475
End page 3480
Publisher Royal Society of Chemistry
Place of publication Cambridge, England
Publication date 2002
ISSN 0959-9428
1364-5501
Summary A new series of ionic liquids based on the thiocyanate anion has been prepared. Incorporation of this anion with an imidazolium, tetraalkylammonium or pyrrolidinium cation produces ionic liquids with advantageously low melting points and good thermal stability. The low temperature phase behaviour of the salts has been investigated using differential scanning calorimetry and multiple solid phases have been observed. The electrochemical windows of representative imidazolium and pyrrolidinium species have been investigated by cyclic voltammetry and determined to be 2.4 and 3.5 V, respectively. In addition, the solid-state structure of N,N-dimethylpyrrolidinium thiocyanate has been determined by X-ray crystallography. This is the first reported structure of a pyrrolidinium thiocyanate species and shows a layered structure with linear thiocyanate groups having bond lengths comparable to those observed in similar SCN−-containing species.
Language eng
Field of Research 039999 Chemical Sciences not elsewhere classified
Socio Economic Objective 970103 Expanding Knowledge in the Chemical Sciences
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2002, The Royal Society of Chemistry
Persistent URL http://hdl.handle.net/10536/DRO/DU:30030240

Document type: Journal Article
Collection: Institute for Technology Research and Innovation
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