Abstract
Chiral molecules and materials have attracted tremendous research interests owing to their intriguing chiral structure and promising application, whereas precise and modular construction toward chiral structures and frameworks is the cornerstone for their development. Herein, a modular synthetic method toward chiral π-conjugated macrocycles (CCMs) incorporating well-defined helical tetraarylethene (TAE) moiety is established, which can feasibly afford chiral porous organic polymers (POPs) with mirror-imaged chirality and hierarchical porous structure via Yamamoto polymerization. These chiral macrocyclic molecules and chiral macrocyclic POPs all show bright emission in solid states owing to the aggregation-induced emission property of the TAE units, and exhibit mirror-imaged circularly polarized luminescence (CPL) with luminescence asymmetric factor on the level of 10-3. Accommodation of Rhodamine B as guest molecules into chiral POPs has contributed to color-tunable CPL-active materials owing to chirality transfer and energy transfer from chiral porous polymers to non-chiral guest dyes. And the chiral luminescent POPs are further utilized to detect explosive molecules via fluorescent quenching, and display enantio-selective sensing of chiral nitro-aromatics. These results have provided a reliable protocol for developing luminescent chiral porous materials, and will further spur the applications of chiral luminescent polymers.
Supplementary materials
Title
Hierarchical Chiral Luminescent Macrocyclic Porous Organic Polymer from Chiral Macrocyclic AIEgens
Description
Hierarchical chiral macrocyclic porous organic polymers (POP) had been synthesized from chiral macrocyclic AIEgens with defined helicality. Circularly polarized luminescence (CPL) had been explored for these polymers and monomers. Furthermore, color-tunable CPL systems were constructed from based on chirality transfer and energy transfer from POPs to dye guest. The POPs were further utilized to enantio-selectively detect chiral amines.
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