(
E,E)-2,7-
Bis(3,4,5-trimethoxyphenylethenyl)fluorene,
1, and a segmented copolymer
2 composed ofthe same chromophore alternated with nonconjugated 1,6-hexanediyl (
alt-oligo(2,6-dimethoxylphenylene-4-vinylene-[9,9-diethylfluoren-2-yl-7-vinylene]-3,5-dimethoxy-phenylene-4-[1,6-hexanedioxyl]) were synthesized. They have solution photoluminescence emission maxima at 420-460 nm, with quantumefficiencies of 0.93 and 0.68, respectively, in chloroform. Electroluminescent spectra in an LEDconfiguration ITO/PEDOT-PSS/(
1 or
2)/Ca-Al
both showed maxima at 470-480 nm, although thespectrum from
2 was significantly
broader. The luminance of LEDs with
1 was over 10-fold higher thanthose with copolymer
2, 0.515 versus 0.040 cd/A, with turn-on voltages of 3 and 5 V, respectively. Thecrystallography of
1 showed no chromophore
-stacking; this a
bsence should limit tendencies for emissionwavelength shifts due to solid state interchromophore interactions. When
1 was heated in air
beforeincorporation into an LED emissive layer, a 540 nm emission component was produced, which did
notoccur if
1 was not heated
before use. Emissive layers of
1 with PMMA gave stronger luminance thaneither neat
1 or
2, with only a modest increase in turn-on voltage. A 10% (w/w)
1:PMMA
based LEDemission showed a maximum at 444 nm (
blue emission with CIE color coefficients of (0.153,0.312)),with a luminance efficiency of 4.5 cd/A and a turn on voltage of 4.5 V.