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An unusual alkylidyne homologation
Author(s) -
Yong-Shen Han,
Anthony F. Hill,
Richard Y. Kong
Publication year - 2018
Publication title -
chemical communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.837
H-Index - 333
eISSN - 1364-548X
pISSN - 1359-7345
DOI - 10.1039/c8cc00119g
Subject(s) - triple bond , dash , chemistry , medicinal chemistry , stereochemistry , double bond , organic chemistry , computer science , operating system
The reaction of [W([triple bond, length as m-dash]CH)Br(CO) 2 (dcpe)] (dcpe = 1,2-bis(dicyclohexylphosphino)ethane) with BuLi and SiCl 4 affords the trichlorosilyl ligated neopentylidyne complex [W([triple bond, length as m-dash]C Bu)(SiCl 3 )(CO) 2 (dcpe)]. This slowly reacts with H 2 O to afford [W([triple bond, length as m-dash]CCH 2 Bu)Cl 3 (dcpe)] and ultimately H 2 C[double bond, length as m-dash]CH Bu via an unprecedented alkylidyne homologation in which coordinated CO is the source of the additional carbon atom with potential relevance to the Fischer-Tropsch process.

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