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Photomechanical Luminescence from Through-Space Conjugated AIEgens.
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2019-12-06 , DOI: 10.1002/anie.201913383 Jingjing Guo 1 , Jianzhong Fan 2 , Xinzhi Liu 1 , Zujin Zhao 1 , Ben Zhong Tang 1, 3
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2019-12-06 , DOI: 10.1002/anie.201913383 Jingjing Guo 1 , Jianzhong Fan 2 , Xinzhi Liu 1 , Zujin Zhao 1 , Ben Zhong Tang 1, 3
Affiliation
Transforming molecular motions into the macroscopic scale is a topic of great interest to nanoscience. The photomechanical effect is a promising strategy to achieve this goal. Herein, we report an intriguing photomechanical luminescence driven by the photodimerization of 2-phenylbenzo[b]thiophene 1,1-dioxide (P-BTO) in molecular crystals and elucidate the working mechanism and substituent effect through crystallographic analysis and theoretical calculations. Striking splitting, hopping, and bending mechanical behaviors accompanied by a significant blue fluorescence enhancement are observed for P-BTO crystals under UV light, which is attributed to the formation of photodimer 2P-BTO. Although 2P-BTO is poorly π-conjugated because of the central cyclobutane ring, it exhibits prominent through-space conjugation and aggregation-induced emission (AIE), affording strong solid-state blue fluorescence at 415 nm with an excellent quantum yield of up to 96.2 %.
中文翻译:
通过空间共轭AIEgens的光机械发光。
将分子运动转化为宏观尺度是纳米科学非常感兴趣的话题。光机械效应是实现该目标的有前途的策略。在本文中,我们报告了由2-苯基苯并[b]噻吩1,1-二氧化物(P-BTO)在分子晶体中的光二聚化驱动的有趣的光机械发光,并通过晶体学分析和理论计算阐明了其工作机理和取代基效应。在紫外光下,P-BTO晶体观察到了明显的分裂,跳跃和弯曲机械行为,并伴有明显的蓝色荧光增强,这归因于光致二聚体2P-BTO的形成。尽管由于中心环丁烷环的缘故,2P-BTO的π共轭性很差,但它仍表现出突出的贯穿空间共轭和聚集诱导发射(AIE),
更新日期:2019-12-06
中文翻译:
通过空间共轭AIEgens的光机械发光。
将分子运动转化为宏观尺度是纳米科学非常感兴趣的话题。光机械效应是实现该目标的有前途的策略。在本文中,我们报告了由2-苯基苯并[b]噻吩1,1-二氧化物(P-BTO)在分子晶体中的光二聚化驱动的有趣的光机械发光,并通过晶体学分析和理论计算阐明了其工作机理和取代基效应。在紫外光下,P-BTO晶体观察到了明显的分裂,跳跃和弯曲机械行为,并伴有明显的蓝色荧光增强,这归因于光致二聚体2P-BTO的形成。尽管由于中心环丁烷环的缘故,2P-BTO的π共轭性很差,但它仍表现出突出的贯穿空间共轭和聚集诱导发射(AIE),