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Ferroelastic-like transition and solvents affect the magnetism of a copper-organic radical one-dimensional coordination polymer.
Gao, Yan-Li; Nishihara, Sadafumi; Suzuki, Takashi; Umeo, Kazunori; Inoue, Katsuya; Kurmoo, Mohamedally.
Afiliação
  • Gao YL; School of Chemistry and Chemical Engineering, Yulin University, Yulin 719000, China.
  • Nishihara S; Department of Chemistry and Center for Chiral Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8526, Japan. kxi@hiroshima-u.ac.jp.
  • Suzuki T; Department of Chemistry and Center for Chiral Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8526, Japan. kxi@hiroshima-u.ac.jp.
  • Umeo K; Department of Chemistry and Center for Chiral Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8526, Japan. kxi@hiroshima-u.ac.jp.
  • Inoue K; Department of Chemistry and Center for Chiral Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8526, Japan. kxi@hiroshima-u.ac.jp.
  • Kurmoo M; Institut de Chimie de Strasbourg, CNRS-UMR7177, Université de Strasbourg, 4 rue Blaise Pascal, 67070 Strasbourg, France. kurmoo@unistra.fr.
Dalton Trans ; 51(17): 6682-6686, 2022 May 03.
Article em En | MEDLINE | ID: mdl-35411897
ABSTRACT
The one-dimensional coordination polymers {[CuII(hfac)2]3(m-BNN)}n·nCH2Cl2 (1·CH2Cl2, P1̄) and {[CuII(hfac)2]3(m-BNN)}n (1', P2/n), hfac = hexafluoroacetylacetonate and m-BNN = meta-phenylene bis(nitronyl-nitroxide), were obtained from CH2Cl2 and CHCl3, respectively. 1·CH2Cl2 is transformed to 1 at 335 K. Their magnetic susceptibilities differ in both magnitude and temperature dependence behavior. 1 and 1' undergo a ferroelastic-like phase transition at 110 K and an unidentified one at 37 K. There is a subtle long relaxation of this ferroelastic-like ordered state.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article