Volume 2016, Issue 5 p. 623-627
Communication

Synthesis and Structure of Lewis‐Base‐Free Phosphinoalumane Derivatives

Tomohiro Agou

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

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Shin Ikeda

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

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Takahiro Sasamori

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

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Norihiro Tokitoh

Corresponding Author

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

Institute for Chemical Research, Kyoto University Gokasho, Uji, Kyoto 611‐0011, JapanSearch for more papers by this author
First published: 13 November 2015
Citations: 4

Abstract

Lewis‐base‐free diphosphinoalumane and 1‐hydro‐2‐chlorophosphinoalumane derivatives bearing a bulky aryl substituent were synthesized by the reaction of the corresponding lithium phosphide and dichloroalumane. Structures of these phosphinoalumane derivatives were determined by spectroscopic and X‐ray crystallographic analyses. Because of the efficient steric protection by the bulky aryl substituent, the aluminum centers in these phosphinoalumane derivatives have tricoordinate geometry. Reactions of the phosphinoalumane derivatives with organolithium reagents and bases were investigated.

Abstract

Lewis‐base‐free diphosphinoalumane and 1‐hydro‐2‐chlorophosphinioalumane derivatives bearing a bulky aryl substituent were synthesized from the corresponding lithium phosphide and dichloroalumane. Their structures were determined spectroscopically and by X‐ray crystallography. Because of the efficient steric protection by the bulky aryl substituent, their aluminum centers are tricoordinate.