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Dimerized p-Semiquinone Radical Anions Stabilized by a Pair of Rare-Earth Metal Ions
Tian Han1, Jonatan B Petersen2, Zi-Han Li1
1School of Science, Frontier Institute of Science and Technology, Research Institute of Xi'an Jiaotong University (Zhejiang), State Key Laboratory for Mechanical Behavior of Materials, MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, and Xi'an Key Laboratory of Sustainable Energy and Materials Chemistry, Xi'an Jiaotong University, Xi'an 710049, China.
Abstract:
Here we report stable p-quinone-radical-bridged rare-earth complexes involving the ligand tetramethylquinone (QMe4•-). The complexes, {Y[(QMe4)•-Cl2(THF)3]}2 (1) and {Gd[(QMe4)•-Cl2(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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