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1,8-Naphthalimide-Based Highly Emissive Luminophors with Various Mechanofluorochromism and Aggregation-Induced Characteristics

[Image: see text] Six 1,8-naphthalimide-based tetraphenylethene derivatives were reported. These highly solid-state emissive compounds showed aggregation-induced emission enhancement or aggregate fluorescence change characteristics. Furthermore, these aggregation-induced green light-emitting or aggr...

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Detalles Bibliográficos
Autores principales: Yin, Ya, Chen, Zhao, Fan, Congbin, Liu, Gang, Pu, Shouzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733177/
https://www.ncbi.nlm.nih.gov/pubmed/31508558
http://dx.doi.org/10.1021/acsomega.9b02110
Descripción
Sumario:[Image: see text] Six 1,8-naphthalimide-based tetraphenylethene derivatives were reported. These highly solid-state emissive compounds showed aggregation-induced emission enhancement or aggregate fluorescence change characteristics. Furthermore, these aggregation-induced green light-emitting or aggregation-induced yellow light-emitting luminophors also exhibited various mechanofluorochromism behaviors involving different fluorescent color changes. To determine the mechanochromic mechanism of these six mechanical stimulus-responsive luminogens, the powder X-ray diffraction (XRD) and X-ray single-crystal measurements were carried out. The powder XRD test results indicated that their interesting mechanofluorochromic behaviors were attributed to the interconversion between crystalline and amorphous states. Meanwhile, the X-ray single-crystal analyses results implied that the twisted molecular conformation and the absence of an intense intermolecular acting force led to a loose packing motif, and the alteration of molecular packing was responsible for the observed mechanofluorochromic effect.