Abstract
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.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
