TY - JOUR
T1 - [FeII(L•)2][TCNQF4•-]2
T2 - A Redox-active Double Radical Salt
AU - Gass, Ian
AU - Lu, Jinzhen
AU - Ojha, Ruchika
AU - Asadi, Mousa
AU - Lupton, David W.
AU - Geoghegan, Blaise
AU - Moubaraki, Boujemaa
AU - Martin, Lisandra L.
AU - Bond, Alan M.
AU - Murray, Keith S.
PY - 2019/6/3
Y1 - 2019/6/3
N2 - The reaction of [FeII(L•)2][BF4]2 with LiTCNQF4 results in the formation of [FeII(L•)2][TCNQF4•-]2·2CH3CN (1) (L• is the neutral aminoxyl radical ligand, 4,4-dimethyl-2,2-di(2-pyridyl)oxazolidine-N-oxide; TCNQF4 is 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane). Single crystal X-ray diffraction; Raman, Fourier transform infrared (FTIR) and ultraviolet-visible (UV-Vis) spectroscopies; and electrochemical studies are all consistent with the presence of: a low-spin FeII ion; the neutral radical form (L•) of the ligand; and the radical anion, TCNQF4•-. 1 is largely diamagnetic and the electrochemistry shows five well resolved, diffusion-controlled, reversible, one electron processes.
AB - The reaction of [FeII(L•)2][BF4]2 with LiTCNQF4 results in the formation of [FeII(L•)2][TCNQF4•-]2·2CH3CN (1) (L• is the neutral aminoxyl radical ligand, 4,4-dimethyl-2,2-di(2-pyridyl)oxazolidine-N-oxide; TCNQF4 is 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane). Single crystal X-ray diffraction; Raman, Fourier transform infrared (FTIR) and ultraviolet-visible (UV-Vis) spectroscopies; and electrochemical studies are all consistent with the presence of: a low-spin FeII ion; the neutral radical form (L•) of the ligand; and the radical anion, TCNQF4•-. 1 is largely diamagnetic and the electrochemistry shows five well resolved, diffusion-controlled, reversible, one electron processes.
KW - Iron
KW - TCNQF4
KW - electrochemistry
KW - radical
KW - redox-active
M3 - Article
SN - 0004-9425
JO - Australian Journal of Chemistry
JF - Australian Journal of Chemistry
ER -