Abstract

We present the experimental results on the third-order nonlinearities of several porphyrin and naphthalocyanine derivatives measured by the femtosecond degenerate four-wave mixing (DFWM) technique under resonant conditions. Studies in the solvent effect on the third-order optical nonlinearities indicate that molecular packing in the solutions has significant effects both on the magnitude of the third-order nonlinear optical susceptibility, &chi;<sup>(3)</sup>, and the DFWM response. The electronic component of the molecular hyperpolarizability, &gamma;<sub>e</sub>, was evaluated to be in the range of 0.9 x 10<sup>-29</sup> esu to 2.3 x 10<sup>-29</sup> esu for these compounds, where the zinc complex of the porphyrin derivative (ZnTTMAPP) showed the largest &gamma;e. These values are two orders of magnitude larger than the reported values measured under non-resonant conditions. The time-resolved results indicate that the relaxation of the excited state population dominates the DFWM response in these macrocycles.

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