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Benzocyclobutenyl functionalized polymers of cyclotrimerized terminal diynes: synthesis and crosslinking
Author(s) -
Gentsy George G.,
Farona Michael F.
Publication year - 1995
Publication title -
polymer international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 105
eISSN - 1097-0126
pISSN - 0959-8103
DOI - 10.1002/pi.1995.210370310
Subject(s) - thermosetting polymer , monomer , benzocyclobutene , polymer chemistry , polymer , materials science , prepolymer , oligomer , copolymer , composite material , polyurethane
The monomers 1,13‐tetradecadiyne, 1,11‐dodecadiyne, 1,9‐decadiyne and 1,7‐octadiyne were cyclotrimerized, using niobium pentachloride as the catalyst, in the presence of 1,5‐hexadiyne, which co‐cyclotrimerizes to give a benzocyclobutene (BCB) capping group. Molecular weights of the BCB‐capped oligomers were in the 3100–8000 range, with fairly narrow polydispersities. The oligomers were characterized by 1 H NMR and IR spectoscopy, along with GPC and DSC studies. DSC studies on the end‐capped oligomers show that each exhibits an exotherm around 260°C, indicative of the formation of carbon–carbon bonds in a crosslinking reaction. The final, crosslinked materials may be regarded as thermosetting thermoplastics, since they are hard at room temperature and soft at 250°C.