Dimerized p-Semiquinone Radical Anions Stabilized by a Pair of Rare-Earth Metal Ions
Author(s) -
Tian Han,
Jonatan B. Petersen,
ZiHan Li,
YuanQi Zhai,
Andreas K. Kostopoulos,
Fabrizio Ortu,
Eric J. L. McInnes,
Richard E. P. Winpenny,
YanZhen Zheng
Publication year - 2020
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.0c00503
Subject(s) - chemistry , semiquinone , rare earth , ion , metal , inorganic chemistry , photochemistry , metal ions in aqueous solution , earth (classical element) , astrobiology , organic chemistry , mineralogy , redox , physics , mathematical physics
Here we report stable p -quinone-radical-bridged rare-earth complexes involving the ligand tetramethylquinone (QMe 4 •- ). The complexes, {Y[(QMe 4 ) •- Cl 2 (THF) 3 ]} 2 ( 1 ) and {Gd[(QMe 4 ) •- Cl 2 (THF) 3 ]} 2 ( 2 ), where THF = tetrahydrofuran, are sufficiently stable that we can measure the single-crystal structures and perform magnetic and electron paramagnetic resonance measurements. These studies show the presence of a semiquinone form and that the magnetic interaction between the radicals in the dimer is strong and antiferromagnetic.
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