Difference between revisions 6001781 and 6001782 on simplewiki{{chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 457631192 | ImageFileL1 = Ferrocene.svg | ImageSizeL1 = 80 px | ImageFileR1 = Ferrocene-from-xtal-3D-balls.png | ImageSizeR1 = 80 px (contracted; show full)|title=The antimalarial ferroquine: from bench to clinic|journal=Parasite|volume=18|issue=3|year=2011|pages=207–214|issn=1252-607X|doi=10.1051/parasite/2011183207|url=http://www.parasite-journal.org/articles/parasite/full_html/2011/03/parasite2011183p207/parasite2011183p207.html|PMID=21894260|PMC=3671469}} {{open access}}</ref><ref>Roux, C.; Biot, C., "Ferrocene-based antimalarials", Future Med. Chem. 2012, 4, 783-797. {{DOI|10.4155/fmc.12.26}}</ref> ===Materials chemistry=== [[File:Wettability of a silica surface with a bound ferrocene-substituted polymer.jpg|left|thumb|500px|Strands of an uncharged ferrocene-substituted polymer are tethered to a [[hydrophobic]] [[silica]] surface. Oxidation of the ferrocenyl groups produces a [[hydrophilic]] surface due to electrostatic attractions between the resulting charges and the polar solvent.<ref name = Pietschnig />]] ⏎ Ferrocene, being readily decomposed to iron nanoparticles, can be used as a catalyst for the production of carbon nanotubes.<ref>{{cite journal|first1=Devin |last1=Conroya |first2=Anna |last2=Moisalab|first3= Silvana |last3=Cardosoa |first4=Alan |last4=Windleb |first5=John |last5=Davidson|journal=[[Chemical Engineering Science|Chem. Eng. Sci.]]|year=2010|volume=65|pages=2965–2977|doi=10.1016/j.ces.2010.01.019|title=Carbon nanotube reactor: Ferrocene decomposition, iron particle growth, nanotube aggreg(contracted; show full) of as a ferrocenyl version of [[polystyrene]] (the phenyl groups are replaced with ferrocenyl groups). Pendant ferrocene units have been attached to both organic and inorganic polymer backbones (such as [[polysiloxane]]s, [[polyphosphazene]]s, and poly[[phosphinoborane]]s, (–PH(R)–BH<sub>2</sub>–)<sub>''n''</sub>) producing materials with unusual physical and electronic properties relating to the ferrocene / ferrocinium redox couple .<ref, such as the changed [[wettability]] of a silica surface with tethered polymer strands.<ref name = Pietschnig>{{cite journal|first = Rudolf|last = Pietschnig|title = Polymers with pendant ferrocenes|journal = [[Chemical Society Reviews|Chem. Soc. Rev.]]|year = 2016|volume = 45|pages = 5216-5231|doi = 10.1039/C6CS00196C}}</ref> ===As a ligand scaffold=== (contracted; show full) {{Authority control}} [[Category:Organoiron compounds]] [[Category:Metallocenes]] [[Category:Antiknock agents]] [[Category:Sandwich compounds]] [[Category:Cyclopentadienyl complexes]] 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=6001782.
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