A room temperature high-spin arylaminium radical polymer satisfying a non-Kekulé and non-disjoint structure was designed and synthesized. A tris(dianisylaminium)triphenylene 3 was synthesized through the oxidative trimerization, the palladium catalyzed amination, and chemical oxidation. The SQUID and NMR shift measurement indicated a quartet state (S = 3/2) for 3 from 2 to 330 K. A model compound 3 was extended to a pseudo two-dimensional poly[anisylaminotris(hexyloxy)triphenylene] 1. Copolycondensation of 2,6,10-tribromo-3,7,11-tris(hexyloxy)triphenylene 4 and 2,6,10-tris(p-anisyl- amino)-3,7,11-tris(hexyloxy)triphenylene 5 using the palladium catalyst gave the polymer 6 with Mn = 5400. This precursor 6 was oxidized to the corresponding polyradical 1. In ΧT values plots, the maximum ΧT value at 3.5 K was 1.38, theoretical value of S = 9/2 is 1.375. These results indicated spin-alignment of the polyradical 1 through the pseudo two-dimensional structure.
|ホスト出版物のタイトル||Polymer Preprints, Japan|
|出版ステータス||Published - 2005|
|イベント||54th SPSJ Symposium on Macromolecules - Yamagata|
継続期間: 2005 9月 20 → 2005 9月 22
|Other||54th SPSJ Symposium on Macromolecules|
|Period||05/9/20 → 05/9/22|
ASJC Scopus subject areas