Difference between revisions 6001592 and 6001593 on simplewiki

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User:Barras/Ferrocene
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| verifiedrevid = 310175235
| ImageFileL1 = Ferrocene-2D.png
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| ImageFileR1 = Ferrocene-from-xtal-3D-balls.png
| ImageSizeR1 = 120 px
| ImageFile2 = Photo of Ferrocene (powdered).JPG
(contracted; show full)ound]]s.<ref>{{cite journal|author=R. Dagani |url=http://pubs.acs.org/isubscribe/journals/cen/79/i49/html/7949sci1.html | title=Fifty Years of Ferrocene Chemistry| journal=[[Chemical and Engineering News]] |date=3 December 2001|volume= 79 |issue= 49 | pages = 37–38 |format=Subscription required}}</ref>  The rapid growth of [[organometallic chemistry]] is often attributed to the excitement arising from the discovery of ferrocene and its many [[Analog (chemistry)|analogues]].

==History==
[[File:
错误的二茂铁结构.pnFerrocene kealy.svg|thumb|left|Pauson and Kealy's original (incorrect) notion of ferrocene's molecular structure]]
Ferrocene was first prepared unintentionally.  In 1951, Pauson and Kealy at [[Duquesne University]] reported the reaction of cyclopentadienyl magnesium bromide and [[iron(III) chloride|ferric chloride]] with the goal of oxidatively coupling the diene to prepare [[fulvalene]]. Instead, they obtained a light orange powder of "remarkable stability."<ref>{{cite journal
(contracted; show full)[[pl:Ferrocen]]
[[ru:Ферроцен]]
[[fi:Ferroseeni]]
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[[th:เฟอร์โรซีน]]
[[tr:Ferrosen]]
[[ur:Ferrocene]]
[[zh:二茂铁]]