Synthesis of Aryl‐Substituted Hexa‐Alkynyl Hexaazatrinaphthylenes via Sonogashira Coupling and Evaluation of Their Photophysical Properties

Hexaazatrinaphthylene (HATNA) has recently been a subject of great interest as a polycyclic heteroaromatic scaffold in materials science, specifically in the field of discotic liquid crystals (DLCs), battery cathodes, n-type semiconductors, and so on. However, little is known about the photophysical properties of HATNA derivatives. Here we report the synthesis of a new class of hexa(arylethynyl) HATNA derivatives via consecutive Sonogashira coupling. This protocol showed good functional-group tolerance and moderate to good yields were achieved. The obtained HATNA products showed favorable photophysical properties, with molar absorption coefficients up to 1.69 × 10<sup>5</sup> (M<sup>-1</sup> cm<sup>-1</sup>) and high quantum yields up to 0.73.

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Journal
Chemistry - An Asian Journal
Published
2026-02-01
DOI
https://doi.org/10.1002/asia.202501003
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
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article

Synthesis of Aryl‐Substituted Hexa‐Alkynyl Hexaazatrinaphthylenes via Sonogashira Coupling and Evaluation of Their Photophysical Properties

Natsuhiko Sugimura, Yuchen Wu, Chisae Kumagai, Takanori Shibata
Chemistry - An Asian Journal
Synthesis and Properties of Aromatic Compounds
article

Synthesis of Aryl‐Substituted Hexa‐Alkynyl Hexaazatrinaphthylenes via Sonogashira Coupling and Evaluation of Their Photophysical Properties

Natsuhiko Sugimura, Yuchen Wu, Chisae Kumagai, Takanori Shibata
article en

Abstract

Hexaazatrinaphthylene (HATNA) has recently been a subject of great interest as a polycyclic heteroaromatic scaffold in materials science, specifically in the field of discotic liquid crystals (DLCs), battery cathodes, n-type semiconductors, and so on. However, little is known about the photophysical properties of HATNA derivatives. Here we report the synthesis of a new class of hexa(arylethynyl) HATNA derivatives via consecutive Sonogashira coupling. This protocol showed good functional-group tolerance and moderate to good yields were achieved. The obtained HATNA products showed favorable photophysical properties, with molar absorption coefficients up to 1.69 × 10<sup>5</sup> (M<sup>-1</sup> cm<sup>-1</sup>) and high quantum yields up to 0.73.

Chemistry - An Asian JournalVol. 21(4)
Waseda University (JP)
Openalex Percentile: Top 50%
Synthesis and Properties of Aromatic Compounds
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Synthesis of Aryl‐Substituted Hexa‐Alkynyl Hexaazatrinaphthylenes via Sonogashira Coupling and Evaluation of Their Photophysical Properties — Natsuhiko Sugimura, Yuchen Wu, et al. · Chemistry - An Asian Journal (2026) | TGRS Research Map | TGRS