A simple and efficient synthesis of di-, tri-, and tetraferrocenylarenes

Masahiko Iyoda; Terumasa Kondo; Toshitaka Okabe; Haruo Matsuyama; Shigeru Sasaki; Yoshiyuki Kuwatani

doi:10.1246/cl.1997.35

A simple and efficient synthesis of di-, tri-, and tetraferrocenylarenes

Masahiko Iyoda, Terumasa Kondo, Toshitaka Okabe, Haruo Matsuyama, Shigeru Sasaki, Yoshiyuki Kuwatani

Research output: Contribution to journal › Article › peer-review

89 Citations (Scopus)

Abstract

A series of di-, tri-, and tetraferrocenylarenes were synthesized by using the nickel- and palladium-catalyzed cross coupling reactions of ferrocenylzinc chloride with the corresponding di-, tri-, and tetrahalogenoarenes. Redox properties of these ferrocenylarenes were studied by cyclic voltammetry in order to examine the intramolecular interaction between the ferrocenyl substituents.

Original language	English
Pages (from-to)	35-36
Number of pages	2
Journal	Chemistry Letters
Issue number	1
DOIs	https://doi.org/10.1246/cl.1997.35
Publication status	Published - 1997 Jan 1
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

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author = "Masahiko Iyoda and Terumasa Kondo and Toshitaka Okabe and Haruo Matsuyama and Shigeru Sasaki and Yoshiyuki Kuwatani",

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T1 - A simple and efficient synthesis of di-, tri-, and tetraferrocenylarenes

AU - Iyoda, Masahiko

AU - Kondo, Terumasa

AU - Okabe, Toshitaka

AU - Matsuyama, Haruo

AU - Sasaki, Shigeru

AU - Kuwatani, Yoshiyuki

PY - 1997/1/1

Y1 - 1997/1/1

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AB - A series of di-, tri-, and tetraferrocenylarenes were synthesized by using the nickel- and palladium-catalyzed cross coupling reactions of ferrocenylzinc chloride with the corresponding di-, tri-, and tetrahalogenoarenes. Redox properties of these ferrocenylarenes were studied by cyclic voltammetry in order to examine the intramolecular interaction between the ferrocenyl substituents.

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A simple and efficient synthesis of di-, tri-, and tetraferrocenylarenes

Abstract

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