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Rhodamine 6G-Labeled Pyridyl Aroylhydrazone Fe(II) Complex Exhibiting Synergetic Spin Crossover and Fluorescence.
Yuan, Juan; Wu, Shu-Qi; Liu, Mei-Jiao; Sato, Osamu; Kou, Hui-Zhong.
Afiliação
  • Yuan J; Department of Chemistry , Tsinghua University , Beijing 100084 , P. R. China.
  • Wu SQ; School of Pharmacy , Henan University of Chinese Medicine , Zhengzhou 450046 , P. R. China.
  • Liu MJ; Institute for Materials Chemistry and Engineering , Kyushu University , 744 Motooka Nishi-ku , 819-0395 Fukuoka , Japan.
  • Sato O; Department of Chemistry , Tsinghua University , Beijing 100084 , P. R. China.
  • Kou HZ; Institute for Materials Chemistry and Engineering , Kyushu University , 744 Motooka Nishi-ku , 819-0395 Fukuoka , Japan.
J Am Chem Soc ; 140(30): 9426-9433, 2018 08 01.
Article em En | MEDLINE | ID: mdl-29983062
Here, we use a pyridinecarbaldehyde rhodamine 6G hydrazone ligand (L) to synthesize an Fe(II) complex 1 for the search of new fluorescent-spin crossover (SCO) materials. Single-crystal structural determinations suggest that the Fe(II) ion is chelated by two ring-opened ligands (L-o) to form a FeN4O2 coordination environment, and intermolecular π---π contacts of the xanthene groups connect the adjacent molecules to form a supramolecular one-dimensional chain. Magnetic susceptibility measurements on complex 1 show that three-step SCO takes place in the temperature range of 120-350 K, and its desolvated form 1-d exhibits SCO around room temperature ( Tc↑ = 343 K and Tc↓ = 303 K) with a wide hysteresis loop of 40 K. Moreover, complex 1-d displays light-induced excited spin-state trapping phenomenon. Intriguingly, the fluorescence intensity of the maximum emission at 560 nm for complex 1-d displays discontinuous variation in the range of 250-400 K, indicative of the occurrence of synergetic fluorescence and SCO.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article