Solvates of a dianisyl-substituted donor-acceptor-type benzothiadiazole: mechanochromic, vapochromic, and acid-responsive multicolor luminescence
Solvates of a dianisyl-substituted donor-acceptor-type benzothiadiazole: mechanochromic, vapochromic, and acid-responsive multicolor luminescence
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二茴香基取代的供体-受体型苯并噻二唑的溶剂化物:机械致色、蒸汽致色和酸响应多色发光
DOI:
10.1039/d2ce01705a
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发表时间:
2023
期刊:
影响因子:
3.1
通讯作者:
Suguru Ito
中科院分区:
文献类型:
--
作者:
Takumi Yagi;Takashi Tachikawa;Suguru Ito
Recently, great advances have been made in the mechanochromic luminescence (MCL) of organic crystals that can switch their emission colors upon exposure to mechanical stimuli. Although several polymorphic crystals and solvates have exhibited multicolor MCL properties, a further deep understanding of the relationship between crystal structures and stimuli-responsive properties is required for rationally generating multicolor-emissive polymorphic crystals and solvates from a single luminescent compound. Herein, multicolor luminescence switching has been achieved for solvates of a phenanthroimidazolylbenzothiadiazole derivative with dianisyl groups. Four types of solvates with different luminescence properties changed their emission colors upon amorphization induced by mechanical stimuli. The amorphous state was recrystallized into solvates when exposed to solvent vapors. Furthermore, the solvate containing pyridine molecules showed a bathochromic shift in emission wavelength upon exposure to acid vapor. Typical acid-responsive luminescence switching is characterized by the protonation of the basic moiety of luminescent molecules, whereas in this study, the change in luminescence color could be induced by protonating non-luminescent pyridine molecules in the solvate. The present study potentially provides useful insights for the development of smart luminescent sensors.