Yt. Chern et al., PREPARATION OF POLYAMIDES DERIVED FROM 1,6-DIAMANTANE DICARBOXYLIC CHLORIDE BY SOLUTION POLYCONDENSATION AND INTERFACIAL POLYCONDENSATION, Journal of polymer science. Part A, Polymer chemistry, 33(16), 1995, pp. 2833-2840
1,6-Diamantane dicarboxylic acyl chloride (I) was used as a monomer wi
th various aromatic diamines to synthesize polyamides by interfacial p
olycondensation and solution polycondensation. The polyamides prepared
by interfacial polycondensation had inherent viscosities between 0.38
and 0.15 dL/g. The polyamides prepared by solution polycondensation h
ad inherent viscosities between 0.62 and 0.25 dL/g. The polyamide IIIa
prepared by solution polycondensation showed the main melting transit
ion at 380 degrees C by dynamic mechanical analysis. In addition, it w
as quite temperature-stable and maintained good mechanical properties
(G' similar to 10(8) Pa) up to high temperatures close to the main tra
nsition well above 350 degrees C. The polyamide IIIa had a tensile str
ength of 35 MPa, elongations to break of 10%, and initial modulus of 0
.8 GPa. Some of the polyamides were soluble in NMP, DMAc, and DMSO, de
pending on soft segment moiety of diamine (II). The polyamides prepare
d by interfacial polycondensation have a greater tendency to form crys
tal than those prepared by solution polycondensation, as evidenced by
x-ray diffraction studies. These polyamides had glass transition tempe
ratures in the 270-300 degrees C range, and 5% weight loss temperature
s up to 435 degrees C in nitrogen. (C) 1995 John Wiley & Sons, Inc.