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Chiral Radical‐Cation Salts of BEDT‐TTF Containing a Single Enantiomer of Tris(oxalato)aluminate(III) and ‐chromate(III)

Authors :
Lee Martin
Michael B. Hursthouse
Peter N. Horton
Ross W. Harrington
Hiroki Akutsu
William Clegg
Source :
European Journal of Inorganic Chemistry. 2015:1865-1870
Publication Year :
2015
Publisher :
Wiley, 2015.

Abstract

Radical-cation salts of BEDT-TTF with chiral anions provide the opportunity to combine chirality with conductivity in the same molecular material. We report here two salts, (BEDT-TTF)3NaAl(C2O4)3·nitromethane and (BEDT-TTF)3(NH4)0.83Cr1.17(C2O4)3·nitromethane. The former crystallises in space group P21 and the latter in P212121. The use of nitromethane alone as the electrolyte for electrocrystallisation produces no crystals, but the addition of chiral (R)-(–)-carvone yields crystals of these two new chiral radical-cation salts of BEDT-TTF through chiral induction from racemic tris(oxalato)aluminate(III) and tris(oxalato)chromate starting materials. The honeycomb anion layers in these salts contain a single enantiomer of tris(oxalato)metallate and creates hexagonal cavities that are smaller than those found in the superconducting β″ salts in this tris(oxalate)metallate family, which gives preference for smaller solvents to be included, such as nitromethane. The chromium salt has a non-stoichiometric composition of the anion layer, which provides an electron doping effect to the donor layer.

Details

ISSN :
10990682 and 14341948
Volume :
2015
Database :
OpenAIRE
Journal :
European Journal of Inorganic Chemistry
Accession number :
edsair.doi...........0d06678932541b009219d0d7ff2aba78
Full Text :
https://doi.org/10.1002/ejic.201500092