Functional bismaleimides containing gamma-lactone, carboxyl, aldehyde, hydr
oxyl, azomethine or cinnamoyl groups were synthesized from maleimido benzoi
c acid via its acid chloride with phenolphtaleine, 5,5'-methylene-bissalicy
lic acid, 5,5'-methylene-bissalicylaldehyde, glycerol, tartaric acid and 3,
4-bis(hydroxyethan-2-tioether)-rho-maleimidobenzoic acid, by simple condens
ation or polymer analogous reactions on some of these reactive bisimides.
The monomers were characterized by IR, H-1-NMR and elemental analysis. The
DSC curves of all the samples showed an exotherm in the temperature range o
f 134-310 degrees C, which is attributable to curing reactions. Thermogravi
metric analysis of the uncured resins indicated good thermal stability and
a char yield of bismaleimide resins in accordance with the calculated C/H r
atio. Their relative thermoxidative stability was evaluated by isothermal g
ravimetric analysis.