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Tunable Circularly Polarized Luminescence from Molecular Assemblies of Chiral AIEgens

submitted on 04.07.2019 and posted on 05.07.2019 by Fengyan Song, yanhua Cheng, Qiuming Liu, Jacky W. Y. Lam, Fafu Yang, Ben Zhong Tang

Circularly polarized luminescence (CPL) is important to chiral photonic technologies. In the molecular systems, besides their intrinsic chemical structures, the architectures of molecular assemblies at the mesoscopic scale also account for the final macroscopic CPL properties. Herein, tunable CPL responses can be induced through architectural regulation of these molecular assemblies in suspension and solid states. A liquid crystalline assembled system of DPCE-ECh exhibiting smectic C* phase with a high dissymmetry factor (gCD = -0.20 and glum = +0.38) is reported. The intense and apparent CD and CPL of the film stem from the intrinsic helical structure of the molecular assembles with weak contribution of Bragg reflection, where the helical axis is perpendicular to the optical axis and is parallel to the direction of the glass substrate. To the best of our knowledge, this large glum factor is very rare for organic compounds even in the assembled state formed by annealing at smectic liquid crystalline temperature. Interestingly, strong CPL signal with glum value of +0.18 is still recorded when DPCE-ECh is annealed at chiral isotropic liquid (Iso*) state. On the other hand, DPCE-ACh can form two coexistence phases of chiral hexagonal and smectic liquid-crystalline phases due to intermolecular hydrogen bonding. The non-periodic molecular orientations of DPCE-ACh break itself helical structure to give a weak negtive CPL signal in 10-3 order. This work thus provides a new insight for developing efficient chiroptical materials in the aggregate state and profound implications in high-performance CPL-based device.


Email Address of Submitting Author


The Hong Kong University of Science and Technology


Hong Kong

ORCID For Submitting Author


Declaration of Conflict of Interest

no conflict of interest