Simultaneous Photo‐Induced Magnetic and Dielectric Switching in an Iron(II)‐Based Spin‐Crossover Hofmann‐Type Metal‐Organic Framework
Molecular materials possessing photo‐tunable polarization switching is promising for optical switches, smart sensors, and data storage devices. However, it is challenging to devise a molecular material featuring simultaneous switchable magnetic and dielectric properties with regard to non‐invasive a...
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Published in | Angewandte Chemie International Edition Vol. 61; no. 45; pp. e202208208 - n/a |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Wiley Subscription Services, Inc
07.11.2022
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Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
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Summary: | Molecular materials possessing photo‐tunable polarization switching is promising for optical switches, smart sensors, and data storage devices. However, it is challenging to devise a molecular material featuring simultaneous switchable magnetic and dielectric properties with regard to non‐invasive and convenient light stimulus. Herein, we report a new Hofmann‐type metal–organic framework (MOF) {Fe(bpt)[Pt(CN)4]} ⋅ 0.5anth (1, bpt=2,5‐bis(4‐pyridyl)thiophen; anth=anthracene), which displays thermo‐ and photo‐switchable magnetic and dielectric properties. Photo‐monitored structural analyses revealed that it was the photo‐induced deformation of FeII coordination sphere and relative movement of guest anthracene that resulted in the variation of the local electric dipoles. These findings provide a new strategy to realize polarization switching through the light‐induced spin crossover, and would be of fundamental significance for future photo‐switchable and multifunctional materials.
A new 3D Hofmann‐type metal–organic framework (MOF) {Fe(bpt)[Pt(CN)4]} ⋅ 0.5anth (1, bpt=2,5‐bis(4‐pyridyl)thiophen; anth=anthracene) is prepared. It displays thermo‐ and photo‐switchable magnetic and dielectric properties accompanied by structural phase transitions between different space groups. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202208208 |