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Updated: May 21, 2025

Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals
Published on: May 29, 2018
Chiral Diazatriptycene Exhibiting Acid-Induced Ternary Circularly Polarized Luminescence Switching and Crystal
Ryo Inoue1, Atsushi Aoki2, Tomohiro Agou1
1Department of Material Science, Graduate School of Science, University of Hyogo, 3-2-1 Kouto, Kamigori-cho, Ako-gun, Hyogo, 678-1297, Japan.
Abstract:
Doubly N-doped triptycene 2,6-diazatriptycene 1 was synthesized as the first example of triptycene-bearing intrinsic chirality in its core. The resolved enantiomers exhibited an acid-induced ternary circularly polarized luminescence (CPL) switching behavior, enabling on/off and +/- control, with a dissymmetry factor (glum) of approximately 10-3. Density functional theory calculations indicated that these ternary CPL changes were derived from modulation of through-space conjugation within the triptycene skeleton. In addition, single-crystal X-ray analysis of 1 and the salt 1•(TfOH)n revealed the presence of herringbone arrangements, trimer clusters, chiral porous tubes, and 2D charge-segregated array structures. These results demonstrate that precise change of the molecular assembly can be achieved using N-doped chiral triptycene facilitated by ionic hydrogen bonding and donor-acceptor π-π stacking.
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