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Other polysubstituted norbornenes

For the ROMP of norbomene attached to C o at the 5,6-positions, see Ch.l4. 13.3.6 Other polysubstituted norbornenes [Pg.313]

Various other polymerizable di-, tri-, and tetra-substituted norbornenes are listed in [Pg.313]

For monomers 124 (62% exo-i-CyfTendo-CV-i, 38% endo-i-C -j-exo-CV, 125 (55% exo-CFs, 45% endo-CF ), and 126 (48% exo-(CF2)3, 52% endo-(CF2)3), the first-named exo-isomer is in each case the more reactive so that if polymerization stops short of 100% conversion, the residual monomer is emiched in the other isomer (Seehof 1993b). [Pg.314]

Films of the polymer of 127 exhibit high permeability to gases because of their high fractional free volume. However, this is offset by a somewhat lower discrimination between different gases, as compared with films of other polymers (Teplyakov 1992). [Pg.314]

Polymers of 128 have a narrow MWD if prepared in THF but not if prepared in chlorobenzene. The polymer has a Tg of 110°C and decomposes at 300°C, losing two molecules of acetic acid per repeat unit. It is also readily hydrolyzed to the polydiol, which is soluble in CF3COOH/CHCI3 and degrades with loss of water at 300°C (Bazan 1991b). [Pg.314]


See other pages where Other polysubstituted norbornenes is mentioned: [Pg.1571]    [Pg.313]    [Pg.1571]    [Pg.313]   


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Norbornen

Norbornene

Polysubstituted

Polysubstitution

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