Difference between revisions 6001798 and 6001799 on simplewiki

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User:Barras/Ferrocene
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| ImageFileL1 = Ferrocene.svg
| ImageSizeL1 = 80 px
| ImageFileR1 = Ferrocene-from-xtal-3D-balls.png
| ImageSizeR1 = 80 px
(contracted; show full)ast3= Ma|first3= Yong-xiang|last4= Liang|first4= Yong-min|last5= Dong|first5= Ning-li|last6= Guan|first6= De-peng|journal=[[Journal of Organometallic Chemistry|J. Organomet. Chem.]]|year=2001|volume=625|pages=128–132|doi=10.1016/S0022-328X(00)00927-X|title=Solvent-free synthesis of ferrocenylethene derivatives}}</ref> The vinyl ferrocene can be converted into a polymer (polyvinylferrocene, PVFc), a ferrocenyl version of [[polystyrene]] (the phenyl groups are replaced with ferrocenyl groups). Another 
[[Polyferrocenes|polymferrocene]] which can be formed is poly(2-(methacryloyloxy)ethyl ferrocenecarboxylate), PFcMA.  In addition to using organic polymer backbones, these pendant ferrocene units have been attached to inorganic backbones such as [[polysiloxane]]s, [[polyphosphazene]]s, and poly[[phosphinoborane]]s, (&ndash;PH(R)&ndash;BH<sub>2</sub>&ndash;)<sub>''n''</sub>, and the resulting materials exhibit unusual physical and electronic properties relating to the ferrocene / ferro(contracted; show full)
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[[Category:Organoiron compounds]]
[[Category:Metallocenes]]
[[Category:Antiknock agents]]
[[Category:Sandwich compounds]]
[[Category:Cyclopentadienyl complexes]]