“…The functional group 2,2,6,6-tetramethylpiperidin- N -oxyl (TEMPO) is a commonly used stable radical in the search for purely organic magnets as well as a paramagnetic marker in biological systems. − Derivatives of the radical have also been employed as electron donors in a number of charge-transfer salts. − In a series of papers Akutsu and co-workers described anions derived from TEMPO with sulfonate groups, where the anionic substituent is connected via a suitable spacer at the 4-position of the piperidine ring (para to the nitroxyl group). Anions containing the amido (−NH−), , oxo (−O−), and acetylamido (−NHC(O)CH 2 −) 46 spacers have been reported, and the ET salt of the last derivative is known, i.e., (ET) 3 (TEMPO−NHCOCH 2 SO 3 ) 2 (H 2 O) 6 …”