Soluble poly(m-phenylenevinylene) derivatives (4) were synthesized via Witt
ig-Horner reaction. The number-average degree of polymerization was estimat
ed to be around 25-35. On the basis of FT-IR and H-1 NMR spectra, the olefi
ns in the polymers were confirmed to be predominantly in the trans-configur
ation. A model compound, 3,5-distyryl-4-hexyloxytoluene (5), was also synth
esized to aid the structural characterization. Comparison of photoabsorptio
n and emission characteristics between 4 and 5 indicated that the m-phenyle
ne effectively interrupted the conjugation, allowing predictable color cont
rol in the pi -conjugated polymers. At low temperature, the fluorescence of
4 was readily resolved into two peaks, suggesting the predominant emission
s were from 0-1 and 0-2 transitions. Polymers 4 were found to be highly lum
inescent in both solution and film states. LED devices using 4 gave blue EL
output (emission lambda (max) at 445 and 462 nm).