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Synthesis of Interlocked and Non-Interlocked Deca(para-phenylene) Derivatives by Ni-mediated Biaryl Coupling.
Ohta, Misuzu; Okuda, Ayano; Hosoya, Shoichi; Yoshigoe, Yusuke; Saito, Shinichi.
Afiliação
  • Ohta M; Department of Chemistry, Tokyo University of Science, 1-3, Kagurazaka, Shinjuku, Tokyo, Japan.
  • Okuda A; Department of Chemistry, Tokyo University of Science, 1-3, Kagurazaka, Shinjuku, Tokyo, Japan.
  • Hosoya S; Research Center for Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, Japan.
  • Yoshigoe Y; Department of Chemistry, Tokyo University of Science, 1-3, Kagurazaka, Shinjuku, Tokyo, Japan.
  • Saito S; Department of Chemistry, Tokyo University of Science, 1-3, Kagurazaka, Shinjuku, Tokyo, Japan.
Chemistry ; 30(16): e202304309, 2024 Mar 15.
Article em En | MEDLINE | ID: mdl-38199956
ABSTRACT
Oligo(para-phenylene) (PPn) is a compound composed of directly connected 1,4-phenylene moieties. The synthesis of PPn composed of six or more phenylene moieties with no substituent at the internal phenylene moiety has been challenging because of its low solubility. Herein we synthesized oligo(para-phenylene)[2]rotaxanes, including a deca(para-phenylene)[2]rotaxane, with a defined number of phenylene moieties. Biaryl coupling of iodoarenes mediated by macrocyclic dibenzodihydrophenanthroline-Ni complex was utilized for the first time to synthesize the [2]rotaxanes. Compared to the non-interlocked deca(para-phenylene), the deca(para-phenylene)[2]rotaxane showed higher solubility. The properties of the oligo(para-phenylene)[2]rotaxanes and non-interlocked oligo(para-phenylene)s were analyzed by spectroscopic methods.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article