Boosting Circularly Polarized Luminescence of Organic Conjugated Systems via Twisted Intramolecular Charge Transfer

通过扭曲的分子内电荷转移增强有机共轭体系的圆偏振发光

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Abstract

Realizing a high luminescence dissymmetry factor (g (lum)) is a paramount yet challenging issue in the research field of circularly polarized luminescence (CPL). Here, we reported a novel set of organic conjugated systems with twisted intramolecular charge transfer (TICT) characteristics based on conjugated o-carborane-binaphthyl dyads composing of binaphthyl units as chiral electron donors and o-carborane units as achiral electron acceptors, demonstrating intense CPL with large g (lum) values. Interestingly, single-crystalline o-1 exhibited a high-level brightness and a large g (lum) factor as high as +0.13, whereas single-crystalline o-2 processed a relatively low brightness with a decreased g (lum) value to -0.04. The significant diversity of CPL-active properties was triggered by the selective introduction of o-carborane units onto the binaphthyl units. Benefiting from the large magnetic dipole transition moments in TICT states, the CPL activity of TICT o-carborane-based materials exhibited amplified circular polarization. This study provides an efficient molecular engineering strategy for the rational design and development of highly efficient CPL-active materials.

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