SYNTHESIS AND CHARACTERIZATION OF 4-CYANOBIPHENYL-4'-YLOXY-FUNCTIONALIZED POLY(7-OXANORBORNENE-5,6-EXO-DICARBOXIMIDE)S VIA RING-OPENING METATHESIS POLYMERIZATION (ROMP)
I. Gangadhara,"campistron et al., SYNTHESIS AND CHARACTERIZATION OF 4-CYANOBIPHENYL-4'-YLOXY-FUNCTIONALIZED POLY(7-OXANORBORNENE-5,6-EXO-DICARBOXIMIDE)S VIA RING-OPENING METATHESIS POLYMERIZATION (ROMP), Journal of polymer science. Part A, Polymer chemistry, 36(15), 1998, pp. 2807-2821
N-[n-(4-cyanobiphenyl-4'-yloxy)alkyl] -7-oxanorbornene-5,6-exo-dicarbo
ximide (CBON2-CBON8) with increasing number of methylene groups in the
alkyl part (n = 2-8) were synthesized by Mitsunobu condensation betwe
en the appropriate alcohols (CBA(2)-CBA(8)) and 7-oxanorbornene-5,6-ex
o-dicarboximide (ON). The conditions for the ring opening metathesis p
olymerization of CBONn giving acceptable molecular weights and molecul
ar distributions were established. Characterization of the resulting p
olymers (P-2-P-8) by H-1- and C-13-NNIR has shown a high trans content
. Differential scanning calorimetry and optical microscopy analysis ha
ve shown that the alcohols CBA(n) are thermotropic with some variation
s between the first and second heating-cooling cycles, the monomers CB
ONn melt with no evidence of any mesomorphic state, the polymers P-n s
how only the glass transition, and the glass transition temperature (T
-g) decreases with increases in the spacer length. (C) 1998 John Wiley
& Sons, Inc.