Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4486
Title: Reactivity of ferrocenylboranes: rearrangements versus electron transfer reactions
Authors: Ding, L.
Fabrizi De Biani, Fabrizia 
Bolte, M.
Zanello, Piero
Wagner, M.
Issue Date: 2000
Project: None 
Journal: ORGANOMETALLICS
Abstract: 
The chemical behavior of ferrocenylboranes FcB(R)R‘ (Fc = C5H5FeC5H4) toward 2,5-bis(pyrazol-1-yl)benzoquinone (1) is highly dependent on the nature of the substituents R and R‘. Reaction of 1 with 2 equiv of the ferrocenylborane FcBMe2 (2a) results in an unprecedented sequence of methyl migration and elimination steps; the Fe(II) oxidation state of the Fc fragments remains unchanged. In contrast, electron-transfer processes involving iron oxidation and benzoquinone reduction dominate the reaction of 1 with FcB(Me)Br (2b) and FcBBr2 (2c). Despite these different reactivities, bis(ferrocenyl) complexes with a bridging hydroquinone ligand (3a, [3b]Br2, [3c]Br2) are formed in all three cases.
Description: 
40310
URI: http://hdl.handle.net/20.500.12779/4486
ISSN: 0276-7333
DOI: 10.1021/om000727w
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