Difference between revisions 6001536 and 6001537 on simplewiki

{{Chembox new
| ImageFileL1 = Ferrocene-2D.png
| ImageSizeL1 = 80 px
| ImageFileR1 = Ferrocene-3D-balls-B.png
| ImageSizeR1 = 120 px
| IUPACName = ferrocene, bis(η<sup>5</sup>-cyclopentadienyl)iron
| OtherNames = ferrocene, iron cyclopentadienyl 
| Section1 = {{Chembox Identifiers
(contracted; show full)
 | title = 2,4-Diferrocenyl-1,3-dithiadiphosphetane 2,4-disulfide; structure and reactions with catechols and [PtCl<sub>2</sub>(PR<sub>3</sub>)<sub>2</sub>](R = Et or Bun)
 | author = Mark R. St. J. Foreman, Alexandra M. Z. Slawin and J. Derek Woollins
 | journal = J. Chem. Soc., Dalton Trans., 
 | year = 1996
 | pages =  3653 &ndash; 3657
 | doi = 10.1039/DT9960003653}}</ref>

[[Image:FcGen'l.png|center|400px|
thumb|Important reactions of ferrocene with electrophiles and other reagents.]]

<br clear = left/>

===Lithiation===
Ferrocene reacts readily with [[butyl lithium]] to give 1,1'-dilithioferrocene, which in turn is a versatile [[nucleophile]]. It has been reported that the reaction of 1,1'-dilithioferrocene with [[selenium]] diethyl[[dithiocarbamate]] forms a strained ferrocenophane where the two cyclopentadienyl ligands are linked by the selenium atom.<ref>Ron Rulkens, Derek P. Gates, David(contracted; show full)[[ja:フェロセン]]
[[pl:Ferrocen]]
[[ru:Ферроцен]]
[[fi:Ferroseeni]]
[[sv:Ferrocen]]
[[tr:Ferrosen]]
[[ur:Ferrocene]]
[[zh:二茂铁]]