Chemistry:Perfluorocycloalkene

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Short description: Class of chemical compounds

A perfluorocycloalkene (PFCA) fluorocarbon structure with a cycloalkene core. PFCAs have shown reactivity with a wide variety of nucleophiles including phenoxides, alkoxides, organometallic, amines, thiols, and azoles.[1] They or their derivatives are reported to have nonlinear optical activity,[2] and be useful as lubricants,[3] etching agents,[4] components of fuel cells,[5] low dielectric materials, and super hydrophobic and oleophobic coatings.[6]

  • Examples of perfluorocycloalkenes

  • Tetrafluorocyclopropene

  • Hexafluorocyclobutene

  • Octafluorocyclopentene

  • Decafluorocyclohexene

Reactivity

Derivatization of these PFCA rings via displacement of fluorine atoms with nucleophiles occurs through an addition-elimination reaction in the presence of a base. Attack of the nucleophile on the PFCA ring generates a carbanion which can eliminate a fluoride ion, resulting in vinyl substituted and allyl substituted products (Scheme 1). The ratio of vinylic to allylic products depends on the ring size, reaction conditions and nucleophile.[1][7]

Derivatization of the PFCA ring.
Scheme 1. Derivatization of the PFCA ring.

[1]

Under favorable conditions, a good nucleophile can replace all the fluorine atoms on PFCA ring (Scheme 2).[8]

Scheme 2. Multi-substitution on PFCA ring

[1][8]

PFCAs have a huge potential to be used as a monomer to produce a variety of polymers. The first time, Smith et al. showed the polycondensation of bisphenols with PFCAs. A unique class of aromatic ether polymers containing perfluorocyclopentenyl (PFCP) enchainment was prepared from the simple step growth polycondensation of commercial available bisphenols and octafluorocyclopentene (OFCP) in the presence of triethylamine (Scheme 3 and 4).[6][9]

Scheme 3. Perfluorocyclopentenyl (PFCP) aryl ether polymer synthesis

[9]

Scheme 4. Bis(heptafluorocyclopentenyl) aryl ether monomers synthesis and polymerization

[9]

Smith et al. further extended his recently published work on perfluorocyclopentenyl (PFCP) aryl ether polymers and perfuorocycloalkenyl (PFCA) aryl ether monomers, and reported the synthesis of a new class of fluoropolymers, namely, perfluorocyclohexenyl (PFCH) aryl ether polymers, via step-growth polycondensation of commercial bisphenols and decafluorocycloalkene (DFCH) in the presence of triethylamine (Scheme 5).[7][10]

Scheme 5. Perfluorocycloalkenyl (PFCA) aryl ether polymer synthesis

[7][10]

References

  1. ↑ 1.0 1.1 1.2 1.3 Wigglesworth, Tony J.; Sud, David; Norsten, Tyler B.; Lekhi, Vikram S.; Branda, Neil R. (2005). "Chiral Discrimination in Photochromic Helicenes". Journal of the American Chemical Society 127 (20): 7272–3. doi:10.1021/ja050190j. PMID 15898750. 
  2. ↑ Matsui, Masaki; Tsuge, Michinori; Funabiki, Kazumasa; Shibata, Katsuyoshi; Muramatsu, Hiroshige; Hirota, Kazuo; Hosoda, Masahiro; Tai, Kazuo et al. (1999). "Synthesis of azo chromophores containing a perfluorocyclo-alkenyl moiety and their second-order optical nonlinearity". Journal of Fluorine Chemistry 97 (1–2): 207–12. doi:10.1016/S0022-1139(99)00050-0. 
  3. ↑ "Organometallic Derivatives Of Perfluorocycloalkenes - Minnesota Mining Mfg Co,Us". 1971-08-25. http://www.freepatentsonline.com/3787461.html. Retrieved 2017-01-05. 
  4. ↑ Takahashi, Kazuo; Itoh, Atsushi; Nakamura, Toshihiro; Tachibana, Kunihide (2000). "Radical kinetics for polymer film deposition in fluorocarbon (C4F8, C3F6 and C5F8) plasmas". Thin Solid Films 374 (2): 303–10. doi:10.1016/S0040-6090(00)01160-3. Bibcode: 2000TSF...374..303T. 
  5. ↑ "Patent US20140162173 - Sulfonated perfluorocyclopentenyl polymers and uses thereof - Google Patents". 2013-10-09. http://www.google.com/patents/US20140162173. Retrieved 2017-01-05. 
  6. ↑ 6.0 6.1 Sharma, Babloo; Verma, Rajneesh; Baur, Cary; Bykova, Julia; Mabry, Joseph M.; Smith, Dennis W. (2013). "Ultra low dielectric, self-cleansing and highly oleophobic POSS-PFCP aryl ether polymer composites". Journal of Materials Chemistry C 1 (43): 7222–7. doi:10.1039/C3TC31161A. https://figshare.com/articles/journal_contribution/2830519. 
  7. ↑ 7.0 7.1 7.2 Sharma, Babloo; Faisal, Mohammad; Liff, Shawna M.; Smith, Dennis W. (2014). "Triarylamine-enchained semifluorinated perfluorocycloalkenyl (PFCA) aryl ether polymers". Applied Petrochemical Research 5: 35. doi:10.1007/s13203-014-0063-0. 
  8. ↑ 8.0 8.1 Garg, Sonali; Twamley, Brendan; Zeng, Zhuo; Shreeve, Jean'neM. (2009). "Azoles as Reactive Nucleophiles with Cyclic Perfluoroalkenes". Chemistry: A European Journal 15 (40): 10554–62. doi:10.1002/chem.200901508. PMID 19746368. 
  9. ↑ 9.0 9.1 9.2 Cracowski, Jean-Marc; Sharma, Babloo; Brown, Dakarai K.; Christensen, Kenneth; Lund, Benjamin R.; Smith, Dennis W. (2012). "Perfluorocyclopentenyl (PFCP) Aryl Ether Polymers via Polycondensation of Octafluorocyclopentene with Bisphenols". Macromolecules 45 (2): 766–71. doi:10.1021/ma2024599. Bibcode: 2012MaMol..45..766C. 
  10. ↑ 10.0 10.1 Sharma, Babloo; Hill, Sarah C.; Liff, Shawna M.; Pennington, William T.; Smith, Dennis W. (2014). "Perfluorocyclohexenyl aryl ether polymers via polycondensation of decafluorocyclohexene with bisphenols". Journal of Polymer Science Part A: Polymer Chemistry 52 (2): 232–8. doi:10.1002/pola.26995. Bibcode: 2014JPoSA..52..232S. https://figshare.com/articles/journal_contribution/2830120. 



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