Organic paraelectrics resulting from tautomerization coupled with proton-transfer

Tadashi Sugawara*, Tomoyuki Mochida, Akira Miyazaki, Akira Izuoka, Naoki Sato, Yoko Sugawara, Kenzo Deguchi, Yutaka Moritomo, Yoshinori Tokura

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

19 被引用数 (Scopus)

抄録

2-Carboxy-3-hydroxyphenalenone was found to behave as paraelectrics at room temperatur under ambient pressure, exhibiting an antiferroelectric transition at 40K. The paraelectric property is derived from an inversion of a transverse component of its dipole moment based on the rapid tautomerization in the solid state. A C2V local symmetry of the molecule revealed by a crystallographic analysis was interpreted in terms of a dynamic disorder based on solid state 13CNMMR (CP/MAS) measurements. The Curie constant determined from a Curie-Weiss plot turned out to be consistent with the above mechanism.

本文言語英語
ページ(範囲)665-668
ページ数4
ジャーナルSolid State Communications
83
9
DOI
出版ステータス出版済み - 1992/09

ASJC Scopus 主題領域

  • 化学一般
  • 凝縮系物理学
  • 材料化学

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