Asymmetric Synthesis of Tetraphenylethylene Helicates and Their Full-Color CPL Emission with High g lum and High Fluorescence Quantum Yield

• Published in: ACS applied materials & interfaces Vol. 15; no. 35; pp. 42056 - 42065
• Main Authors: Ye, Feng-Ying, Hu, Ming, Zheng, Yan-Song
• Format: Journal Article
• Language: English
• Published: American Chemical Society 06.09.2023
• Subjects: Surfaces, Interfaces, and Applications; asymmetric synthesis; chirality transfer and amplification; tetraphenylethylene helicates; circularly polarized luminescence; liquid crystal
• ISSN: 1944-8244; 1944-8252
• DOI: 10.1021/acsami.3c07431

Tetraphenylethylene (TPE) helicates with single helical handedness not only owe high fluorescence quantum yield but also possess good helical chirality, showing an excellent circularly polarized luminescence active material. In this work, a new method for directly obtaining single-handed TPE helicates has been developed. By using chiral p-phenylenediamine derivatives as an intramolecular cyclization reagent of TPE, the single-handed propeller-like conformation and stable helical chirality of the TPE unit were obtained, avoiding complicated and expensive HPLC chiral column separation. The as-prepared chiral TPE helicates displayed strong emission with an almost quantitative fluorescence quantum yield (Φf) and strong circularly polarized luminescence (CPL). In addition, the chirality and CPL signals of the TPE helicates could be significantly magnified by the helical arrangement together with 4′-pentyl-4-biphenylcarbonitrile (5CB) liquid crystal molecules. Moreover, full-color CPL emissions with both a high absolute CPL dissymmetrical factor up to 0.43 and high Φf were afforded.