Triphenylene core has a planar π-conjugated structure which is expected to allow radical generation at low oxidation potential and strong ferromagnetic interaction of the radicals' unpaired electrons. We reported the triradical, 2,6,10-tris(dianisylaminium)-3,7,11-tris(hexyloxy)triphenylene, with a quartet state (S = 3/2) at room temperature. Connection of the module by satisfying non-Kekule and non-disjoint coupling fashion is supposed to yield a stable, high-spin purely organic polyradical. In this report, we designed and have synthesized poly(aminium triphenylene) 1+̇ and poly(naphthylaminium triphenylene) 2+̇ by extending the triradical. Spin alignment of 1+̇ and 2+̇ was discussed by SQUID measurement. It was expected that the quartet triaminium triphenylene module is effectively connected through the triphenylene and naphthalene structures.
|ホスト出版物のタイトル||Polymer Preprints, Japan|
|出版ステータス||Published - 2006|
|イベント||55th Society of Polymer Science Japan Symposium on Macromolecules - Toyama|
継続期間: 2006 9月 20 → 2006 9月 22
|Other||55th Society of Polymer Science Japan Symposium on Macromolecules|
|Period||06/9/20 → 06/9/22|
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