Difference between revisions 6001673 and 6001674 on simplewiki{{chembox | verifiedrevid = 396489042 | ImageFileL1 = Ferrocene.svg | ImageSizeL1 = 80 px | ImageFileR1 = Ferrocene-from-xtal-3D-balls.png | ImageSizeR1 = 120 px | ImageFile2 = Photo of Ferrocene (powdered).JPG | ImageSize2 = 220 px (contracted; show full) The carbon-carbon bond distances are 1.40 Å within the five membered rings, and the Fe-C bond distances are 2.04 Å. ==Synthesis and handling properties== The first reported<ref>{{cite journal|year=1951|last1=Kealy|first1=T. J.|last2=Pauson|first2=P. L.|journal=[[Nature (journal)|Nature]]|volume=168|pages=1039|doi=10.1038/1681039b0 |issue=4285}}</ref> synthesis of ferrocene used the [[Grignard reaction|Grignard reagent]] cyclopentadienyl magnesium bromide, which can be prepared by reacting [[cyclopentadiene]] with magnesium and [[bromoethane]] in [[anhydrous]] [[benzene]]. [[Iron(II) chloride]] is then suspended in anhydrous [[diethyl ether]] and added to the Grignard reagent. The reaction sequence is: (contracted; show full)[[ru:Ферроцен]] [[fi:Ferroseeni]] [[sv:Ferrocen]] [[th:เฟอร์โรซีน]] [[tr:Ferrosen]] [[uk:Фероцен]] [[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=6001674.
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