Force-triggered hypso- and bathochromic bidirectional fluorescence switching beyond 120 nm and its anticounterfeiting applications

Author:

Yin Ya1ORCID,Guan Qichen2ORCID,Chen Zhao1ORCID,Deng Dian-dian1ORCID,Liu Shanting3,Sun Yue4ORCID,Liu Sheng Hua3ORCID

Affiliation:

1. Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013, People’s Republic of China.

2. State Key Laboratory of Separation Membrane and Membrane Process, School of Chemistry, Tiangong University, Tianjin 300387, People’s Republic of China.

3. Xi'an Key Laboratory of Functional Organic Porous Materials, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an 710129, People’s Republic of China.

4. National Key Laboratory of Green Pesticide, College of Chemistry, Central China Normal University, Wuhan 430079, People’s Republic of China.

Abstract

Achieving high-contrast tricolor emissive regulation of a single-component molecule using a single type of external stimulus is highly desirable but challenging. In the present study, we report a symmetric acceptor-donor-acceptor (A-D-A)–type aggregation-induced emission-active luminogen, which displays a sequential high-contrast fluorescence switching just by anisotropic mechanical grinding. Specifically, upon light grinding, an orange–yellow-to-blue hypsochromic mechanofluorochromic response with a distinct color contrast (change in the maximum emission wavelength, Δλ em,max = 122 nm) is noticed, and the slightly ground solid exhibits a blue-to-red high-contrast (Δλ em,max = 185 nm) bathochromic mechanofluorochromic conversion upon vigorous grinding. Thus, using a single luminogen developed here, we can realize wide-range (Δλ em,max > 100 nm) hypso- and bathochromic fluorescence mechanochromisms simultaneously. The tricolored mechanofluorochromic phenomenon is attributed to two different morphological transitions involving crystalline-to-crystalline and crystalline-to-amorphous states. Furthermore, three information anticounterfeiting systems are developed using the luminogen presented here.

Publisher

American Association for the Advancement of Science (AAAS)

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