Efficient π-electron conjugated push–pull nonlinear optical chromophore 1-(4-methoxyphenyl)-3-(3,4-dimethoxyphenyl)-2-propen-1-one: A vibrational spectral study

As part of the efforts for the design new organic nonlinear optical (NLO) materials with high efficiency for present day technological requirements, a comprehensive investigation on the intramolecular charge transfer (ICT) of an efficient π-conjugated potential push–pull NLO chromophore, 1-(4-methoxyphenyl)-3-(3,4-dimethoxyphenyl)-2-propen-1-one to a strong electron acceptor group through the π-conjugated bridge has been carried out from their vibrational spectra. The NIR FT-Raman and FT-IR spectra supported by the density functional theory (DFT) quantum chemical computations have been employed to analyze the effects of intramolecular charge transfer on the geometries and the vibrational modes contributing to the linear electro-optic effect of the organic NLO material. The calculated first hyperpolarizability of DMMC is 6.650 × 10−30 esu, which is 25 times that of urea. The simultaneous IR and Raman activation of the phenyl ring modes of ν(CC/C–C) mode, ring CC stretching modes, in-plane deformation modes and the umbrella mode of methyl groups also provide evidences for the charge transfer interaction between the donors and the acceptor group through the π-system. Vibrational analysis indicates the electronic effects such as induction and back-donation on the methyl hydrogen atoms causing the lowering of stretching wavenumbers have also been analyzed in detail. The planar conformations would give an enhanced NLO activity where as any deviations from planarity would decrease the mobility of electrons within the π-conjugated molecular system, resulting a reduction in NLO activity.