4.8 Article

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

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 52, Pages 27144-27150

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202113294

Keywords

azobenzene; guest-driven light-induced spin change; photo-responsive materials; spin crossover; trans-cis photoisomerization

Funding

  1. National Key Research and Development Program of China [2018YFA0306001]
  2. NSFC [21773316, 21771200, 21821003]
  3. Guangdong Basic and Applied Basic Research Foundation [2020A1515010837]
  4. Pearl River Talent Plan of Guangdong [2017BT01C161]

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This study reports an unprecedented guest-driven light-induced spin change in a Hofmann-type metal-organic framework, where the reversible trans-cis photoisomerization of azobenzene guest results in 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 for the development of a new generation of photo-responsive magnetic materials.
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)(2)}(2)].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.

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