Abstract
Two novel nonlinear optical (NLO) chromophores with 4-hydroxycarbazole as the electron donor were successfully designed and synthesized. The 4-hydroxycarbazole had two reaction sites where the isolated groups were introduced to the chromophores. The prepared chromophores were characterized by MS, 1H NMR and UV–vis spectra. Poled films of the chromophores doped in APC afforded the maximum electro-optic (EO) coefficient (r33) of 40pm/V at 1310nm. This result was better than the similar chromophores reported using carbazole and aniline derivates as electron donor, which indicated that the introduction of isolated groups suppressed the dipole–dipole interaction between chromophores effectively and could aid the alignment of chromophores and improve the EO activity. This had been further demonstrated by the crystal structure analysis.
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