Difference between revisions 6001603 and 6001604 on simplewiki{{chembox | Watchedfields = changed | verifiedrevid = 310175235 | ImageFileL1 = Ferrocene-2D.png | ImageSizeL1 = 80 px | ImageFileR1 = Ferrocene-from-xtal-3D-balls.png | ImageSizeR1 = 120 px | ImageFile2 = Photo of Ferrocene (powdered).JPG (contracted; show full) The carbon atoms can be replaced by heteroatoms as illustrated by Fe(η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>)(η<sup>5</sup>-P<sub>5</sub>) and Fe(η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>)(η<sup>5</sup>-C<sub>4</sub>H<sub>4</sub>N) ("[[azaferrocene]]"). The latterAzaferrocene arises from decarbonylation of Fe(η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>)(CO)<sub>2</sub>(η<sup>1</sup>-pyrrole) in [[cyclohexane]].<ref>{{cite journal|doi=10.1016/0022-328X(90)85359-7|title=An improved photochemical synthesis of azaferrocene|year=1990|last1=Zakrzewski|first1=J|journal=Journal of Organometallic Chemistry|volume=388|pages=175}}</ref> This compound on boiling under [[reflux]] in [[benzene]] is converted to ferrocene.&l(contracted; show full)[[pl:Ferrocen]] [[ru:Ферроцен]] [[fi:Ferroseeni]] [[sv:Ferrocen]] [[th:เฟอร์โรซีน]] [[tr:Ferrosen]] [[ur:Ferrocene]] [[zh:二茂铁]] All content in the above text box is licensed under the Creative Commons Attribution-ShareAlike license Version 4 and was originally sourced from https://simple.wikipedia.org/w/index.php?diff=prev&oldid=6001604.
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