Abstract

Circularly polarized luminescence (CPL) emission materials with high luminescence dissymmetry factor (glum) and high quantum yield (QY) are currently in urgent demand for real applications. Three D-A type enantiomers (R-/S-1, 2 and 3) were designed and synthesized that combine a phenanthro [9,10-d]imidazole (PIP) unit to a naphthalimide (NI) at the p-, m-, o-positions. These AIE-active enantiomers were chosen as CPL emitters doped into nematic liquid crystals (E7, N-LCs) to form three chiral nematic liquid crystals (N*-LCs-1, 2 and 3). Interestingly, N*-LCs-1 shows higher glum (+0.91/-0.98) and QY (18.5%) than N*-LCs-2 (glum = +0.86/-0.89, QY = 1.3%) and N*-LCs-3 (glum = +0.010/-0.013, QY = 4.7%) due to effective chirality transfer and intramolecular electronic coupling from microstructure change of AIE-active isomers. This paper revealed that AI-CD and AI-CPL enhancement behavior of N*-LCs could be regulated not only by the chirality transfer via supramolecular self-assembly but also by the electronic coupling strength through microstructure change of AIE-active isomers of donor units in the chiral emitters. This work can provide a new strategy for the development of CPL LCs materials.

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