Synthesis of Optically Active Tolane‐Stacked Molecules Based on Planar Chiral [2.2]Paracyclophanes

Abstract In this study, optically active compounds were synthesized by stacking diarylacetylenes with two benzene rings and an ethynylene (tolane derivatives) using planar chiral [2.2]paracyclophanes. The compounds with carboxy groups formed one‐dimensional zig‐zag structures through hydrogen bonds in the crystals, with three hydrogen‐bonded chains bundled to construct a one‐handed triple helix. All compounds prepared in this study exhibited circularly polarized luminescence properties with good anisotropy factors.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-02-03
DOI
https://doi.org/10.1002/ajoc.202400624
Citations
1
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.94
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article

Synthesis of Optically Active Tolane‐Stacked Molecules Based on Planar Chiral [2.2]Paracyclophanes

Ryo Inoue, Yasuhiro Morisaki, Takanori Ito, Shun Yukimoto
1 citations
Asian Journal of Organic Chemistry
Synthesis and Properties of Aromatic Compounds
0.94
article

Synthesis of Optically Active Tolane‐Stacked Molecules Based on Planar Chiral [2.2]Paracyclophanes

Ryo Inoue, Yasuhiro Morisaki, Takanori Ito, Shun Yukimoto
article en
1 citations

Abstract

Abstract In this study, optically active compounds were synthesized by stacking diarylacetylenes with two benzene rings and an ethynylene (tolane derivatives) using planar chiral [2.2]paracyclophanes. The compounds with carboxy groups formed one‐dimensional zig‐zag structures through hydrogen bonds in the crystals, with three hydrogen‐bonded chains bundled to construct a one‐handed triple helix. All compounds prepared in this study exhibited circularly polarized luminescence properties with good anisotropy factors.

Asian Journal of Organic ChemistryVol. 14(4)
University of Hyogo (JP), Kwansei Gakuin University (JP)
Openalex Percentile: Top 29%
Synthesis and Properties of Aromatic Compounds
0.94
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