I. Mcculloch et al., SIDE-CHAIN PENDANT NONLINEAR OPTICALLY-ACTIVE POLYMERS SYNTHESIZED BYGRAFTING REACTIONS ON MALEIC-ANHYDRIDE COPOLYMERS, Macromolecular chemistry and physics, 197(2), 1996, pp. 687-699
The synthesis of well defined, high molecular weight polymers for non-
linear optical (NLO) applications has been carried out in an effort to
improve the film properties of waveguides fabricated from these mater
ials. Free radical methods of polymerisation result in molecular weigh
t limitations due to the chain transfer nature of the NLO active chrom
ophores, and therefore, in order to prepare a high molecular weight po
lymer, a post polymerisation grafting method was chosen to incorporate
side chain pendant chromophores onto a preformed polymer. Alcoholysis
of anhydride copolymers resulted in chromophore incorporation levels
of up to 90% of available reactive sites. Additional branching of the
linear anhydride prepolymers was also carried out using polytetrahydro
furan but this was not shown to improve the mechanical properties of t
he fabricated films. Since the anhydride opens to an ester and an acid
, in order to reduce the ionic content of the final polymer, further r
eaction of the generated carboxylic acid group was attempted, resultin
g in partial diester formation, and an improvement in film quality. El
ectrical field poling at temperatures close to the glass transition wa
s only successful at low electrical field strengths, allowing electroo
ptic coefficients of values of up to 2.4 pm/V at a poling field of 80
V/mu m to be obtained.