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Photoconvertible precursors of 2,6-linked anthracene oligomers (trimer, tetramer, and pentamer) were synthesized through repeated Suzuki-Miyaura cross-coupling reactions. Upon exposure of these precursors to light at 450 nm, which correspond to the n–pi* transition of diketone moieties, yellow precipitates were formed, suggesting the conversion to the corresponding anthracene oligomers from the precursors. The disappearance of 1H NMR peaks after photoirradiation indicated the formation of anthracene oligomers with less solubility. High-resolution mass spectrometry evidently indicated the oligomer formations, and infrared spectral analysis for thin films showed the disappearance of peaks originating from the carbonyl groups, also supporting the conversion. The absorption spectra after photoirradiation indicated a red-shift in the absorption peaks accompanying oligomer formations, suggesting an extension of the pi-conjugated system. The low solubility of the resulting anthracene oligomers in organic solvents highlights the effectiveness of this synthetic strategy using the photoconvertible precursor. This study provides a practical method to synthesize acene oligomers without the introduction of extra substituents.

権利情報:

• Creative Commons BY-NC Attribution-NonCommercial 4.0 International
  

キーワード: anthracene, multi-step synthesis, oligomer, photoconversion, precursor approach

刊行年月日: 2025-08-22

出版者: Wiley

掲載誌:

• European Journal of Organic Chemistry (ISSN: 1434193X) vol. 28 issue. 31 e202500490

研究助成金:

• Japan Science and Technology Corporation JPMJPR21AC
• Foundation for Nara Institute of Science and Technology
• Iketani Science and Technology Foundation
• Tokyo Ohka Foundation for The Promotion of Science and Technology

原稿種別: 出版者版 (Version of record)

MDR DOI:

公開URL: https://doi.org/10.1002/ejoc.202500490

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更新時刻: 2025-08-29 08:30:16 +0900

MDRでの公開時刻: 2025-08-29 08:19:27 +0900