发光
光致发光
费斯特共振能量转移
材料科学
分子
聚合物
偶极子
接受者
共振感应耦合
共轭体系
小分子
光电子学
光化学
化学物理
分子物理学
能量转移
化学
光学
荧光
凝聚态物理
物理
复合材料
生物化学
有机化学
作者
Jessica Wade,Jochen R. Brandt,D.L. Reger,Francesco Zinna,Konstantin Amsharov,Norbert Jux,Davıd L. Andrews,Matthew J. Fuchter
标识
DOI:10.1002/anie.202011745
摘要
Abstract Strongly dissymmetric circularly polarised (CP) luminescence from small organic molecules could transform a range of technologies, such as display devices. However, highly dissymmetric emission is usually not possible with small organic molecules, which typically give dissymmetric factors of photoluminescence ( g PL ) less than 10 −2 . Here we describe an almost 10 3 ‐fold chiroptical amplification of a π‐extended superhelicene when embedded in an achiral conjugated polymer matrix. This combination increases the | g PL | of the superhelicene from approximately 3×10 −4 in solution to 0.15 in a blend film in the solid‐state. We propose that the amplification arises not simply through a chiral environment effect, but instead due to electrodynamic coupling between the electric and magnetic transition dipoles of the polymer donor and superhelicene acceptor, and subsequent CP Förster resonance energy transfer. We show that this amplification effect holds across several achiral polymer hosts and thus represents a simple and versatile approach to enhance the g‐factors of small organic molecules.
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