Ryota Iwamori
;
Junpei Kuwabara
;
Takeshi Yasuda
(National Institute for Materials Science
)
;
Takaki Kanbara
Description:
(abstract)We explored the appropriate monomer structures and reaction conditions for the site- and regio-selective hydroarylation polyaddition of PAHs using a Co-catalyst. As poly(naphthalene) and poly(naphthalenevinylene) derivatives linked at β-positions show high fluorescence quantum yields (Φ > 0.7) and have been applied to OLEDs, 2,6-di(1-pyrazolyl)naphthalene was designed as a new naphthalene monomer. A site- and regio-selective hydroarylation polyaddition proceeded smoothly under mild reaction conditions to obtain the corresponding PAV. In addition, this monomer design was applicable to the hydroarylation polyaddition of a carbazole unit. Furthermore, the optical and electronic properties of the synthesized PAVs were evaluated.
Rights:
This is the peer reviewed version of the following article: R. Iwamori, J. Kuwabara, T. Yasuda, T. Kanbara, Molecular Design of Naphthalene- and Carbazole-Based Monomers for Regiospecific Synthesis of Poly(arylenevinylene)s via Co-Catalyzed Hydroarylation Polyaddition. Macromol. Rapid Commun. 2024, 45, 2400168, which has been published in final form at https://doi.org/10.1002/marc.202400168. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.
Keyword: Hydroarylation Polyaddition, Poly(arylenevinylene)s, Regiospecific Synthesis, Organic light-emitting diode
Date published: 2024-04-21
Publisher: Wiley
Journal:
Funding:
Manuscript type: Author's version (Accepted manuscript)
MDR DOI: https://doi.org/10.48505/nims.4705
First published URL: https://doi.org/10.1002/marc.202400168
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Updated at: 2025-04-21 12:30:09 +0900
Published on MDR: 2025-04-21 12:20:35 +0900
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