Abstract
Two principally novel organic nonlinear optical chromophores (1 and 2) with flexible (n-hexyl group) or rigid isolated (benzyl group) group are designed and successfully synthesized. The prepared chromophores were characterized by MS, 1H-NMR and UV–Vis spectra. Their thermal stability was studied by thermal gravimetric analyzer and differential scanning calorimetry. Poled films of the chromophores doped in amorphous polycarbonate afford the maximum electro-optic tensor coefficient (r33) equal to 39 pm/V, 63 pm/V for chromophore 1 and chromophore 2, respectively at the wavelength 1,064 nm. The reason of so large differences between these two chromophores’ linear electrooptics coefficients were explained within a framework of performed quantum chemical calculations and it is crucially dependent on distances between the chromophore molecules and the polymer chains.
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Acknowledgments
We are grateful to the Directional Program of the Chinese Academy of Sciences (KJCX2.YW.H02) and Innovation Fund of the Chinese Academy of Sciences (CXJJ-11-M035) for financial support.
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Liu, J., Franiv, A.V., Liu, X. et al. Enhanced electrooptical active materials based on n-hexyl group flexible isolation in NLO chromophores. J Mater Sci: Mater Electron 24, 2701–2705 (2013). https://doi.org/10.1007/s10854-013-1158-6
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DOI: https://doi.org/10.1007/s10854-013-1158-6