A variety of allylamine-adducted bismaleimide (A-BMI) resins were prep
ared by reacting bismaleimide (BMI), such as 4,4'-bismaleimidodiphenyl
methane (BDM) and 4,4'-bis-maleimidodiphenylether (BDE), with various
molar ratio of allylamine through the Michael addition. The prepared A
-BMI resins are a partial crystalline or completely amorphous solid, d
epending on the amount of adducted allylamine. Two types of curing rea
ctions for the A-BMI resins were detected by differential scanning cal
ormetry and verified by the mass spectroscopies of cured resins: one i
s the homopolymerization of A-BMI resins through opening of the double
bonds in the maleimide groups; the other is the reactions between all
yl groups and benzene rings, taking place mainly when most of the doub
le bonds in maleimide groups of the A-BMI resins have been opened by a
llylamines. (C) 1993 John Wiley & Sons, Inc.