Difference between revisions 6001560 and 6001561 on simplewiki{{chembox | ImageFileL1 = Ferrocene-2D.png | ImageSizeL1 = 80 px | ImageFileR1 = Ferrocene-from-xtal-3D-balls.png | ImageSizeR1 = 120 px | ImageFile2 = Photo of Ferrocene (powdered).JPG | ImageSize2 = 220 px | ImageName2 = Powdered Ferrocene (contracted; show full)llic chemistry. In 1973 [[Ernst Otto Fischer|Fischer]] of the [[Ludwig-Maximilians-Universität München]] and [[Geoffrey Wilkinson|Wilkinson]] of [[Imperial College London]] shared a Nobel Prize with for their work on metallocenes and other aspects of organometalic chemistry.<ref>{{cite web |url=http://nobelprize.org/nobel_prizes/chemistry/laureates/1973/press.html |title= Press Release: The Nobel Prize in Chemistry 1973 |year= 1973 |publisher= The Royal Swedish Academy of Sciences}}</ref> == Bonding and StructureStructure and bonding== The iron atom in ferrocene is normally assigned to the +2 oxidation state, as can be shown using [[Mössbauer spectroscopy]]. Each cyclopentadienyl (Cp) ring is then allocated a single negative charge, bringing the number of π-electrons on each ring to six, and thus making them [[aromaticity|aromatic]]. These twelve electrons (six from each ring) are then shared with the metal ''via'' covalent bonding, which, when combined with the six ''d''-electrons on Fe<sup&(contracted; show full)[[pl:Ferrocen]] [[ru:Ферроцен]] [[fi:Ferroseeni]] [[sv:Ferrocen]] [[th:Ferrocene]] [[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=6001561.
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