4.8 Article

Three-Step Spin State Transition and Hysteretic Proton Transfer in the Crystal of an Iron(II) Hydrazone Complex

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 59, 期 35, 页码 14781-14787

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202006763

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资金

  1. MEXT KAKENHI [JP19K15524, JP17H01197, JP16H00849, JP17K05761, JP24109014, JP15K13710, JP17H03117, JP16K05421, JP17H06928, JP20K15247]
  2. MEXT
  3. JST-CREST Innovative Catalysts [JPMJCR15P5]
  4. Cooperative Research Program of Network Joint Research Center for Materials and Devices
  5. Nanotechnology Platform Program (Molecule and Material Synthesis) of MEXT, Japan

向作者/读者索取更多资源

A proton-electron coupling system, exhibiting unique bistability or multistability of the protonated state, is an attractive target for developing new switchable materials based on proton dynamics. Herein, we present an iron(II) hydrazone crystalline compound, which displays the stepwise transition and bistability of proton transfer at the crystal level. These phenomena are realized through the coupling with spin transition. Although the multi-step transition with hysteresis has been observed in various systems, the corresponding behavior of proton transfer has not been reported in crystalline systems; thus, the described iron(II) complex is the first example. Furthermore, because proton transfer occurs only in one of the two ligands and yr electrons redistribute in it, the dipole moment of the iron(II) complexes changes with the proton transfer, wherein the total dipole moment in the crystal was canceled out owing to the antiferroelectric-like arrangement.

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