End group chemistry of fluoro-oligomers: Highly selective syntheses of diepoxy, diallyl, and tetraol derivatives

Journal of Polymer Science, Part A: Polymer Chemistry

Volumn 34, Issue 16, 1996, Pages 3263-3275

  Turri, Stefano ^a   Scicchitano, Massimo ^a   Tonelli, Claudio ^a  

^a Ausimont SpA   (Italy)

Author keywords

Allyl; Chemical modification; End group chemistry; Epoxide; Etherification; Fluoropolyether; NMR; Oligomer; Oxidation; Polyol; Tetraol

Indexed keywords

ALLYL RESINS; CHEMICAL BONDS; CHEMICAL MODIFICATION; DERIVATIVES; EPOXY RESINS; FLUORINE CONTAINING POLYMERS; MOLECULAR STRUCTURE; MONOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION; SYNTHESIS (CHEMICAL);

END GROUP CHEMISTRY; ETHERIFICATION; FLUOROPOLYETHER; POLYFUNCTION FLUORINATED OLIGOMERS; POLYHYDROXY END GROUPS; POLYOL; TETRAOL;

OLIGOMERS;

EID: 0030284240     PISSN: 0887624X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0518(19961130)34:16<3263::AID-POLA2>3.0.CO;2-V     Document Type: Article

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