A series of epoxy-based second-order nonlinear optical (NLO) polymers
containing heteroaromatic chromophores have been designed. Precursor p
olymers were prepared from the polymerization between the diglycidyl e
ther of Bisphenol A and aniline or 4-(2-thienyl)aniline. The precursor
polymers were postfunctionalized by an ate-coupling reaction as well
as tricyanovinylation to form a series of NLO polymers containing hete
roaromatic chromophores. We have extended and established the versatil
ity of our earlier reported postmodification strategy to include vario
us heteroaromatic chromophores in the polymers at the final stage of s
ynthesis. The correlation between different heteroaromatic chromophore
structures and the NLO properties of the polymers was extensively stu
died during this work. Polymers containing heteroaromatic chromophores
exhibit improved temporal stability and enhanced NLO activity. The d(
33) value of 80 pm/V at 1.550 mu m was observed for a representative p
olymer of the class containing 2-(4-aminophenyl)-(5-tricyanovinyl)thio
phene chromophores. NLO properties of the poled polymers exhibit long-
term stability at 80 degrees C.