Volume 7, Issue 2 p. 298-300
Communication

Evidence for LiBr‐Assisted Generation of a Silylene from a 1,2‐Diaryl‐1,2‐dibromodisilene

Dr. Joon Soo Han

Nano‐Materials Research Center, Korea Institute of Science and Technology, 39‐1 Hawolgok‐dong, Seongbuk‐gu, Seoul 136‐791 (Korea)

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Prof. Dr. Takahiro Sasamori

Corresponding Author

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209Search for more papers by this author
Prof. Dr. Yoshiyuki Mizuhata

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209

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Prof. Dr. Norihiro Tokitoh

Corresponding Author

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611‐0011 (Japan), Fax: (+81) 774‐38‐3209Search for more papers by this author
First published: 01 December 2011
Citations: 21

Abstract

Instant silylene! LiBr assists the dissociation of 1,2‐diaryl‐1,2‐dibromodisilenes. Reactions with various trapping agents gave products identical to those from corresponding reactions with aryl bromosilylenes. The reaction provides a method for the in situ generation of silylenes under mild conditions, and the reaction rate is increased by the addition of LiBr.

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