Affiliation:
1. College of Biological and Pharmaceutical Sciences China Three Gorges University Yichang Hubei 443002 P. R. China
2. College of Materials and Chemical Engineering China Three Gorges University Yichang Hubei 443002 P. R. China
3. State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Chemistry and Chemical Engineering Donghua University Shanghai 201620 P.R. China
Abstract
AbstractLow‐molecular‐weight organogels with ultra‐long room temperature phosphorescent (RTP) are ideal materials for dynamic anti‐counterfeiting, due to their sensitive thermal‐responsive character. However, it is a great challenge to realize ultra‐long RTP in a single‐component organogel because conventional auxiliary groups for the promotion of gel formation are usually flexible, which increases non‐radiative decay through molecular motions to quench the RTP. Non‐conventional organogelators with rigid chemical structures may be able to alleviate the non‐radiative decay to maintain the phosphorescent characters in the gel state like in the crystalline state. In this work, potential low‐molecular weight phosphorescent organogelators with rigid chemical structures are predicted by using the descriptors derived from all‐atom molecular dynamics simulation, and successfully screen out two RTP non‐conventional organogelators. It is exciting that one of them exhibited ultra‐long RTP in the gel state. Furthermore, triplet‐to‐singlet Forster resonance energy transfer between the RTP gelator (donor) and fluorescent sulforhodamine 101 (SR101) (acceptor) in the gel state provided a long‐lived red fluorescence. Due to the sensitive thermal‐responsive property of organogel, the afterglow can be well switched between “on” and “off” with excellent fatigue‐resistant properties, which is promising for dynamic anti‐counterfeiting.
Funder
National Natural Science Foundation of China
Subject
Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
3 articles.
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