Synthesis of Interlocked and Non‐Interlocked Deca(para‐phenylene) Derivatives by Ni‐mediated Biaryl Coupling

Author:

Ohta Misuzu1,Okuda Ayano1,Hosoya Shoichi2,Yoshigoe Yusuke1,Saito Shinichi1ORCID

Affiliation:

1. Department of Chemistry Tokyo University of Science 1-3, Kagurazaka, Shinjuku Tokyo Japan

2. Research Center for Medical and Dental Sciences Tokyo Medical and Dental University 1-5-45, Yushima, Bunkyo-ku Tokyo Japan

Abstract

AbstractOligo(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.

Funder

Japan Society for the Promotion of Science

Promotion and Mutual Aid Corporation for Private Schools of Japan

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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