Volume 2016, Issue 5 p. 678-684
Full Paper

Selenium‐Substituted Phosphaalk­enes Obtained through 1,2‐Elimination of Chlorosilanes from Selenen­ylchlorophosphines

Takahiro Sasamori

Corresponding Author

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011, Japan http://boc.kuicr.kyoto‐u.ac.jp/www/

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011, JapanSearch for more papers by this author
José Manuel Villalba Franco

Institut für Anorganische Chemie der Rheinische Friedrich‐Wilhelms‐Universität Bonn, Gerhard‐Domagk‐Str. 1, 53121 Bonn, Germany

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Jing‐Dong Guo

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011, Japan http://boc.kuicr.kyoto‐u.ac.jp/www/

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Koh Sugamata

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011, Japan http://boc.kuicr.kyoto‐u.ac.jp/www/

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Shigeru Nagase

Fukui Institute for Fundamental Chemistry, Kyoto University, Kyoto, Kyoto 606‐8103, Japan

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Rainer Streubel

Institut für Anorganische Chemie der Rheinische Friedrich‐Wilhelms‐Universität Bonn, Gerhard‐Domagk‐Str. 1, 53121 Bonn, Germany

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Norihiro Tokitoh

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011, Japan http://boc.kuicr.kyoto‐u.ac.jp/www/

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First published: 21 December 2015
Citations: 4

Abstract

Stable selenenyl‐chlorophosphines, bearing a silylalkyl group, were synthesized. Subsequent treatment with Lewis acids such as AlCl3 afforded the corresponding phosphaalkenes. A reaction mechanism that proceeds through an intramolecular 1,2‐elimination of chlorosilane was proposed.

Abstract

Stable selenenyl‐chlorophosphines, bearing a trisilylalkyl group, were synthesized, and their treatment with Lewis acids such as AlCl3 afforded the corresponding phosphaalkenes. The experimental results and theoretical calculations suggested that the reaction proceeds through the intramolecular 1,2‐elimination of chlorosilanes