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Two-Step Thermoinduced Metal-to-Metal Electron Transfer and ON/OFF Photoswitching in a Molecular [FeCo] Square Complex. | LitMetric

AI Article Synopsis

  • A cyanide-bridged [FeCo] molecular square complex has been created and thoroughly analyzed using various methods like X-ray diffraction and magnetic measurements.
  • The complex undergoes a two-step spin transition due to metal-to-metal electron transfer, shifting from a low-temperature diamagnetic state to a high-temperature paramagnetic state under specific temperature conditions.
  • Additionally, it can reversibly switch states when exposed to different light wavelengths, showing significant thermal hysteresis effects even at temperatures below 100 K.

Article Abstract

A cyanide-bridged [FeCo] molecular square complex, {[Fe(Tp)(CN)][Co()]}(BF)·2CHCN·6HO [; Tp = hydrotris(pyrazol-1-yl)borate and = bis(1-ethyl-1-imidazol-2-yl)ketone], has been synthesized and characterized fully by single-crystal X-ray diffraction, (photo)magnetic measurements, optical reflectivity, and other physical measurements. exhibits a two-step metal-to-metal electron-transfer (MMET)-induced spin transition accompanied by thermal hysteresis (↑ = 332 and 407 K and ↓ = 320 and 405 K, respectively), converting the low-temperature diamagnetic {Fe-CN-Co} ground state into the high-temperature paramagnetic {Fe-CN-Co} state. Additionally, displays reversible photoinduced MMET under light irradiation (ON mode using 808 nm laser light and OFF mode using 532 nm laser light), as confirmed by optical reflectivity and (photo)magnetic measurements. The photoinduced paramagnetic metastable state relaxes back to the diamagnetic ground state at 91 K ( = 91 K). Astonishingly, also exhibits a 27 K wide light-induced thermal hysteresis below 100 K. The overall results show that is a multistimuli-responsive bistable material that exhibits reversible switching between the diamagnetic state, {Fe-CN-Co}, and the paramagnetic state, {Fe-CN-Co}, under the application of temperature and light.

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Source
http://dx.doi.org/10.1021/acs.inorgchem.0c02053DOI Listing

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