A Photomagnetic Sponge: High-Temperature Light-Induced Ferrimagnet Controlled by Water Sorption

“Converting” light energy to magnetization is the attribute of molecule-based compounds called photomagnets and is inaccessible for conventional magnetic solids. The design and synthesis of such compounds, however, is a formidable challenge, and only a few examples are known, all with rather low mag...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the American Chemical Society Vol. 140; no. 46; pp. 15876 - 15882
Main Authors: Magott, Michał, Reczyński, Mateusz, Gaweł, Bartłomiej, Sieklucka, Barbara, Pinkowicz, Dawid
Format: Journal Article
Language:English
Published: United States American Chemical Society 21-11-2018
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:“Converting” light energy to magnetization is the attribute of molecule-based compounds called photomagnets and is inaccessible for conventional magnetic solids. The design and synthesis of such compounds, however, is a formidable challenge, and only a few examples are known, all with rather low magnetic ordering temperatures well below the boiling point of liquid nitrogen. Herein, a cyanide-bridged coordination polymer, {[MnII(imidazole)]2[WIV(CN)8]} n , exhibiting the highest light-induced magnetic ordering temperature ever observed and a magnetic hysteresis loop up to 90 K is reported. The photomagnetic effect results from the blue light excitation (450 nm) of the constituent octacyanotungstate­(IV) moiety, which then couples magnetically with manganese­(II), resulting in light-induced ferrimagnetic ordering. The reported coordination framework shows also outstanding water sorption properties that are strongly correlated with the photomagnetic functionality. The photoswitching observed in the anhydrous state is completely quenched by the reversible capture of water, with the fully hydrated phase becoming practically non-photomagnetic.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.8b09322