Author(s): Mitsunori Nobusawa, Hiroki Akutsu, Jun-ichi Yamada and Shinichi Nakatsuji
Page: [685 - 688] Pages: 4
* (Excluding Mailing and Handling)
A couple of TEMPO-substituted anthraquinone isomers showed marked difference regarding solvating properties and the resulting magnetic behavior: without obstruction an isomer includes solvent molecules as benzene or acetonitrile to form crystals exhibiting different intermolecular magnetic interactions, while another isomer gives solvent-free crystals showing singlet-triplet behavior.
Keywords: Organic radical, TEMPO radical, anthraquinone, magnetic property, crystal structure
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