One‐pot Syntheses of Benzo‐ and Benzofuran‐fused Iridaoxabenzenes via CH Bond Activations of Alkyl‐bridged Diphenol Derivatives

Author:

Iwamoto Takahiro1ORCID,Suzuki Mika1,Hasegawa Hibiki1,Abeta Hinako1,Matsuo Yusuke2,Tanaka Takayuki3,Yasuda Nobuhiro4,Ishii Youichi1ORCID

Affiliation:

1. Department of Applied Chemistry Faculty of Science and Engineering Chuo University 1-13-27 Kasuga, Bunkyo-ku Tokyo 112-8551 Japan

2. Department of Chemistry Graduate School of Science Kyoto University Sakyo-ku Kyoto 606-8502 Japan

3. Department of Molecular Engineering Graduate School of Engineering Kyoto University, Nishikyo-ku, Kyoto 615–8510 (Japan)

4. Japan Synchrotron Radiation Research Institute 1-1-1 Kouto, Sayo-cho, Sayo-gun Hyogo 679-5198 Japan

Abstract

AbstractOne‐pot syntheses of new π‐extended metallaaromatic compounds have been developed by utilizing Ir‐mediated CH bond activation of ethylene‐ or ethylidene‐bridged diphenol derivatives. Depending on the bridging alkyl groups, two types of iridaoxabenzenes, both of which are doubly fused with benzo and benzofuran units, have been obtained. Studies on their structures and electronic characters indicate that both complexes have an aromatic character on the iridaoxacycles, and their π‐conjugated systems are fully delocalized over the whole molecular skeletons. These novel metallaaromatic complexes exhibited some reactivities which are distinct from those reported for the non‐fused metallaaromatic compounds.

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

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