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客体驱动的负载偶氮苯金属有机框架中的光诱导自旋变化

Guest-Driven Light-Induced Spin Change in an Azobenzene Loaded Metal-Organic Framework.

作者信息

Xie Kai-Ping, Ruan Ze-Yu, Lyu Bang-Heng, Chen Xiao-Xian, Zhang Xue-Wen, Huang Guo-Zhang, Chen Yan-Cong, Ni Zhao-Ping, Tong Ming-Liang

机构信息

Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2021 Dec 20;60(52):27144-27150. doi: 10.1002/anie.202113294. Epub 2021 Nov 17.

Abstract

Stimuli-responsive materials that can be reversibly switched by light are of immense interest. Among them, photo-responsive spin crossover (SCO) complexes have great promises to combine the photoactive inputs with multifaceted outputs into switchable materials and devices. However, the reversible control the spin-state change by photochromic guests is still challenging. Herein, we report an unprecedented guest-driven light-induced spin change (GD-LISC) in a Hofmann-type metal-organic framework (MOF), [Fe(bpn){Ag(CN) } ]⋅azobenzene. (1, bpn=1,4-bis(4-pyridyl)naphthalene). The reversible trans-cis photoisomerization of azobenzene guest upon UV/Vis irradiation in the solid-state results in the remarkable magnetic changes in a wide temperature range of 10-180 K. This finding not only establishes a new switching mechanism for SCO complexes, but also paves the way toward the development of new generation of photo-responsive magnetic materials.

摘要

能够通过光进行可逆切换的刺激响应材料备受关注。其中,光响应自旋交叉(SCO)配合物极有希望将光活性输入与多方面输出结合到可切换材料和器件中。然而,通过光致变色客体对自旋态变化进行可逆控制仍然具有挑战性。在此,我们报道了在一种霍夫曼型金属有机框架(MOF)[Fe(bpn){Ag(CN)}]⋅偶氮苯(1,bpn = 1,4 - 双(4 - 吡啶基)萘)中前所未有的客体驱动光诱导自旋变化(GD - LISC)。固态下偶氮苯客体在紫外/可见光照射下的可逆反式 - 顺式光异构化导致在10 - 180 K的宽温度范围内出现显著的磁性变化。这一发现不仅为SCO配合物建立了一种新的切换机制,也为新一代光响应磁性材料的开发铺平了道路。

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