کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1324384 | 1499895 | 2013 | 9 صفحه PDF | دانلود رایگان |
• The first borylated [3]ferrocenophanes have been prepared.
• In [3]Fc–BBr2, the boryl group is bent toward the Fe center by a dip angle of 26°.
• Borylated [3]ferrocenophanes provide facile access to brominated [3]ferrocenophanes.
• Brominated [3]ferrocenophanes readily undergo Stille-type coupling reactions.
• [3]Fc–Bpin and Li[AlH4] give the unique organyl(trihydrido)borate Li[[3]Fc–BH3].
Treatment of [3]ferrocenophane (1) with 0.7 eq. or 3 eq. of BBr3 in hexane at reflux temperature gives the corresponding dibromoboryl (2) or 1,1′-bis(dibromoboryl) derivative (3) in good yields. Compounds 2 and 3 can be transformed into the corresponding di(tert-butoxy)boryl (4, 5) and pinacolboryl [3]ferrocenophanes (6, 7). Reaction of 6 and 7 with aqueous CuBr2 in MeOH/iPrOH at reflux temperature leads to the formation of the mono- and 1,1′-di-brominated [3]ferrocenophanes 8 and 9; subsequent Stille-type C–C-coupling reactions with nBu3SnPh yield mono- and 1,1′-di-phenylated [3]ferrocenophanes. Treatment of 6 with Li[AlH4] in Et2O at −78 °C provides access to the monotopic lithium trihydridoborate 12.
[3]Ferrocenophane readily undergoes electrophilic borylation with BBr3; the resulting mono- and di-borylated species provide facile access to the corresponding brominated [3]ferrocenophanes, which serve as useful starting materials for Stille coupling reactions.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 744, 1 November 2013, Pages 15–23