In this study, a new photochromic organic molecule was successfully synthesized and applied to the construction of a photochromic luminescent sensor. The sensor showed high sensitivity in detecting Cu2+ and MnO4- in aqueous medium and demonstrated good recyclability.
Photochromic materials have shown very promising applications. However, developing new photochromic materials remains a huge challenge. In this work, a new photochromic organic molecule, namely 6,13-bis(di(pyridin-4-yl)methylene)-6,13-dihydropentacene (L), has been successfully synthesized. Its photochromic mechanism has been elucidated. The dihydropentacene-based photochromic organic molecule was firstly applied as functional ligands to construct LMOF-based sensor {Zn(L)(TPA)center dot H2O}(n) (1; LMOF = luminescent metal-organic framework; H(2)TPA = terephthalic acid). 1 exhibits a three-dimensional (3-D) two-fold interpenetrated architecture, excellent stabilities, luminescent and photochromic properties. 1 can highly sensitively detect Cu2+ and MnO4- in aqueous medium by luminescent quenching effect. Notably, the quenching constants of 1' (1 after photochromism) towards Cu2+ and MnO4- are 6.4 and 6.5 times higher than those of 1, respectively, which demonstrates significantly enhanced sensing sensitivities for 1'. Furthermore, 1' can effectively identify MnO4- from similar strong oxidizing anions CrO42- and Cr2O72-. This dual-response luminescent sensor exhibits good recyclability, and its quenching sensing mechanisms have been discussed in detail. This work will contribute to the development of efficient photochromic luminescent sensors.
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