Photoinduced Regio- and Stereoselective Introduction of Phenylchalcogeno Moieties to Ethynylferrocene
Upon photoirradiation, diphenyl diselenide and diphenyl ditelluride reacted with ethynylferrocene to afford the corresponding bischalcogenated vinylferrocenes. Regio- and stereoselectivities were determined by X-ray crystal analysis, and redox properties were investigated by cyclic voltammetry.
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Veröffentlicht in: | Bulletin of the Chemical Society of Japan 2014-04, Vol.87 (4), p.550-552 |
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container_title | Bulletin of the Chemical Society of Japan |
container_volume | 87 |
creator | Nomoto, Akihiro Hayashi, Satoko Fujiyama, Takuya Ikeda, Takuma Hirata, Kiichi Tohoma, Jun Kakiuchi, Kiyomi Nakanishi, Waro Ogawa, Akiya |
description | Upon photoirradiation, diphenyl diselenide and diphenyl ditelluride reacted with ethynylferrocene to afford the corresponding bischalcogenated vinylferrocenes. Regio- and stereoselectivities were determined by X-ray crystal analysis, and redox properties were investigated by cyclic voltammetry. |
doi_str_mv | 10.1246/bcsj.20130160 |
format | Article |
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source | Oxford University Press Journals All Titles (1996-Current) |
subjects | Crystals Selenides Stereoselectivity Voltammetry X-rays |
title | Photoinduced Regio- and Stereoselective Introduction of Phenylchalcogeno Moieties to Ethynylferrocene |
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