Synthesis and characterization of highly soluble 9,10-diphenyl-substituted poly(2,6-anthracenevinylene)

We report the synthesis and optoelectronic properties of highly soluble poly(9,10-bis(3′,4′-di(2″-ethylhexyloxy))phenyl)-2,6-anthracenevinylene) (HSM-PAV). The key intermediate for the synthesis of HSM-PAV is 2,6-dimethyl-9,10-dibromoanthracene, and the high solubility of HSM-PAV is from the incorporation of lateral 3,4-di(2-ethylhexyloxy)phenyl moieties into the 9,10-positions of anthracene units. The increase of side alkyloxy groups endows HSM-PAV with higher molecular weight (Mn = 3.2 × 104) and better electroluminescence performances (Lmax = 590 cd/m2, LEmax = 0.27 cd/A) compared with the poly(2,6-anthracenevinylene) with lateral monoalkyoxy moieties (Mn = 1.9 × 104, Lmax = 340 cd/m2, LEmax = 0.17 cd/A). The electrical conductivity of doped HSM-PAV film with iodine is 5 × 10−2 S cm−1 that is several order higher than that of doped 9,10-anthracene-based polymers, further demonstrating that linkage position has a dramatic effect on the optoelectronic properties of anthracene-based conjugated polymers.