Hironobu Hayashi
(Center for Basic Research on Materials/Advanced Materials Characterization Field/Nanoprobe Group, National Institute for Materials Science
)
;
Juanjuan Zhu
(NAIST)
;
Naoto Minamino
(NAIST)
;
Yuya Murakami
(NAIST)
;
Shoma Kasahara
(Institute for Chemical Research)
;
Kyohei Matsuo
(Institute for Chemical Research)
;
Naoki Aratani
(NAIST)
;
Hiroko Yamada
(Institute for Chemical Research)
説明:
(abstract)Ethynylene-bridged acenes, which are pi-conjugated triple bond-containing systems, have attracted increasing interest as promising organic semiconductor materials due to their delocalized pi-electrons. In this study, ethynylene-bridged pentacene precursor oligomers were not only synthesized through multiple-organic reactions but also were unexpectedly obtained in one-pot by using a conventional reaction with lithium silylacetylide and quinone. In the case of one-pot synthesis, the formation of oligomers, including pentamer, was evidently confirmed by matrix-assisted-laser-desorption/ionization time-of-flight mass spectrometry. Single crystal X-ray analysis visualized the ethynylene-bridged structure of the dimer which was one of the major products in the one-pot reaction. It was found that the reaction time for the lithiation was the key factor in controlling oligomer formation. Finally, the thermal conversion from pentacene precursors to the corresponding pentacene oligomers was achieved via retro-Diels–Alder reaction. These results would open an access to synthesize a wide range of pi-conjugated systems.
権利情報:
キーワード: pentacene, oligomer, thermal conversion, single crystal, precursor approach
刊行年月日: 2024-12-09
出版者: Wiley-Blackwell
掲載誌:
研究助成金:
原稿種別: 著者最終稿 (Accepted manuscript)
MDR DOI: https://doi.org/10.48505/nims.5063
公開URL: https://doi.org/10.1002/ejoc.202400770
関連資料:
その他の識別子:
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更新時刻: 2025-08-13 08:30:36 +0900
MDRでの公開時刻: 2025-08-13 08:17:13 +0900
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Accepted_MS_MDR.pdf
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サイズ | 964KB | 詳細 |