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The second main synthesis road for perfluorodecanoic acid used commercially is [[telomerization]].<ref name="Mel">Melissa M. Schultz, Douglas F. Barofsky, and Jennifer A. Field. Fluorinated Alkyl Surfactants. Environmental Engineering Science. Sep 2003. 487-501. [[doi:10.1089/109287503768335959]]. Published in Volume: 20 Issue 5: July 6, 2004 </ref> Since PFDA has an even number of carbons, the starting material should be pentafluoroethyl iodide.<ref name="Swed"/> The process follows the general scheme:<ref name="Mel"/> |
The second main synthesis road for perfluorodecanoic acid used commercially is [[telomerization]].<ref name="Mel">{{Cite journal |doi=10.1089/109287503768335959 |title=Fluorinated Alkyl Surfactants |date=2003 |last1=Schultz |first1=Melissa M. |last2=Barofsky |first2=Douglas F. |last3=Field |first3=Jennifer A. |journal=Environmental Engineering Science |volume=20 |issue=5 |pages=487–501 }}</ref> Since PFDA has an even number of carbons, the starting material should be pentafluoroethyl iodide.<ref name="Swed"/> The process follows the general scheme:<ref name="Mel" /> |
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'''Telomerization''' |
'''Telomerization''' |
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Tetrafluoroethylene |
Tetrafluoroethylene |
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