Article Molecular Design of Naphthalene‐ and Carbazole‐Based Monomers for Regiospecific Synthesis of Poly(arylenevinylene)s via Co‐Catalyzed Hydroarylation Polyaddition

Ryota Iwamori ; Junpei Kuwabara ; Takeshi Yasuda SAMURAI ORCID (National Institute for Materials ScienceROR) ; Takaki Kanbara

Collection

Citation
Ryota Iwamori, Junpei Kuwabara, Takeshi Yasuda, Takaki Kanbara. Molecular Design of Naphthalene‐ and Carbazole‐Based Monomers for Regiospecific Synthesis of Poly(arylenevinylene)s via Co‐Catalyzed Hydroarylation Polyaddition. Macromolecular Rapid Communications. 2024, 45 (16), 2400168. https://doi.org/10.1002/marc.202400168
SAMURAI

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:

  • In Copyright

    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:

  • Macromolecular Rapid Communications (ISSN: 10221336) vol. 45 issue. 16 2400168

Funding:

  • Japan Society for the Promotion of Science 23KJ0240

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

Related item:

Other identifier(s):

Contact agent:

Updated at: 2025-04-21 12:30:09 +0900

Published on MDR: 2025-04-21 12:20:35 +0900

Filename Size
Filename Iwamori_MARC24_SI.pdf (Thumbnail)
application/pdf
Size 1.99 MB Detail
Filename Iwamori_MARC24.pdf
application/pdf
Size 762 KB Detail