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Updated: May 27, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Large-Area, Ultra-thin Organic Films with Both Photochromic and Phosphorescence Properties
Chuanli Chen1, Weijing Zhang2, Zeng Wang3
1School of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, 325035, P. R. China.
Abstract:
Polyethylene terephthalate (PET), polystyrene (PS), and polyvinyl chloride (PVC) are the most commonly used polymers in plastic products. Therefore, endowing these polymers with unique optical properties would significantly enhance their overall technological value. Herein, we synthesized a phosphorescent molecule, 2,2'-diphenyl-3,3'-bibenzofuran (DBF), with notable reversible photochromic properties (switching between colorless and deep red) as the guest and constructed a doped system with the above polymers as the hosts. All doped materials exhibited both room-temperature phosphorescence and reversible photochromic properties. The guest molecule exhibited strong reversible cyclization activity and small conformational changes during the reaction process, as well as moderate rigidity of the host matrix, which enabled the uncommon coexistence of these two properties in the doped system. Finally, DBF/PET was successfully formed into a transparent and uniform film with a length of 200 m, a width of 20 cm, a thickness of only 60-70 μm. This film exhibited excellent thermal-stability, sensitivity, and resistance to photo-fatigue, indicating its applicability in industrial production.
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