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Blackmore, P.M. and Feast, W.J. (1988) Stereoregular Fluoropolymers: 6. The Ring-Opening Polymerization of N- Pentafluorophenylbicyclo[2.2.1]hept-5-ene-2,3-dicarboximide. Journal of Fluorine Chemistry, 40, 331-347.
http://dx.doi.org/10.1016/S0022-1139(00)83072-9

has been cited by the following article:

• TITLE: Synthesis of New Polymer Ionomers via Ring-Opening Metathesis Polymerization

  AUTHORS: A. A. Santiago, J. Vargas, Jorge A. Cruz-Morales, M. A. Tlenkopatchev, R. Gaviño, Yu. A. Malkanduev, N. A. Sivov

  KEYWORDS: Polynorbornene Dicarboximide, Ring-Opening Metathesis Polymerization, Ionomers

  JOURNAL NAME: Open Journal of Organic Polymer Materials, Vol.4 No.4, October 28, 2014

  ABSTRACT: The N-pentafluorophenyl-exo-endo-norbornene-5,6-dicarboximide (2a) and N-phenyl-exo-endo-nor-bornene-5,6-dicarboximide (2b) monomers were synthesized and polymerized via ring-opening metathesis polymerization (ROMP) using bis(tricyclohexylphosphine) benzylidene ruthenium(IV) dichloride (I) and tricyclohexylphosphine [1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene][benzylidene] ruthenium dichloride (II). Both catalysts were used to synthesize random and block high molecular weight copolymers which were further hydrogenated using a Wilkinson’s catalyst. Then, the saturated copolymers were modified by reacting with sodium 4-hydroxybenzene-sulfonate dihydrate to generate new ionomers with fluoro-sulfonic acid pendant groups.