Tian Shuai, Ma Huili, Wang Xuan, Lv Anqi, Shi Huifang, Geng Yun, Li Jie, Liang Fushun, Su Zhong-Min, An Zhongfu, Huang Wei
Institute of Organic Luminescent Materials (IOLM), College of Chemistry, Liaoning University, 66 Chongshan Mid. Road, Shenyang, 110036, China.
Key Laboratory of Flexible Electronics (KLOFE) &, Institute of Advanced Materials (IAM), Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing, 211800, China.
Angew Chem Int Ed Engl. 2019 May 13;58(20):6645-6649. doi: 10.1002/anie.201901546. Epub 2019 Apr 1.
Developing pure organic materials with ultralong lifetimes is attractive but challenging. Here we report a concise chemical approach to regulate the electronic configuration for phosphorescence enhancement. After the introduction of d-pπ bonds into a phenothiazine model system, a phosphorescence lifetime enhancement of up to 19 times was observed for DOPPMO, compared to the reference PPMO. A record phosphorescence lifetime of up to 876 ms was obtained in phosphorescent phenothiazine. Theoretical calculations and single-crystal analysis reveal that the d-pπ bond not only reduces the (n, π*) proportion of the T state, but also endows the rigid molecular environment with multiple intermolecular interactions, thus enabling long-lived phosphorescence. This finding makes a valuable contribution to the prolongation of phosphorescence lifetimes and the extension of the scope of phosphorescent materials.
开发具有超长寿命的纯有机材料很有吸引力,但具有挑战性。在此,我们报告一种简洁的化学方法来调节电子构型以增强磷光。在将d-pπ键引入吩噻嗪模型体系后,与参比物PPMO相比,观察到DOPPMO的磷光寿命增强高达19倍。在磷光吩噻嗪中获得了高达876 ms的创纪录磷光寿命。理论计算和单晶分析表明,d-pπ键不仅降低了T态的(n, π*)比例,还赋予刚性分子环境多种分子间相互作用,从而实现长寿命磷光。这一发现为延长磷光寿命和扩展磷光材料范围做出了有价值的贡献。