Nonlinear optical properties of novel tunable, one dimensional molecular superlattice polymers (heteroarylene methines) containing alternating aromatic and quinoid segments

Abstract

We have investigated the spectral dispersion of second molecular hyperpolarizability γ (−ω′; ω, −ω, ω) of three derivatives of heteroarylene methine by antiresonant ring interferometric nonlinear spectroscopic technique using femtosecond modelocked Ti:sapphire laser in the spectral range of 725–820 nm. The observed dispersion of γ has been explained in the framework of three-essential states model involving the ground state, a one-photon excited state and a two-photon excited state. The spectral response of the hyperpolarizability has been correlated with the electronic and chemical structures of the three derivatives of heteroarylene methine. The estimated γ values have been compared to the fundamental quantum mechanical limit. We have found for the first time that the heteroarylene methines approach this limit within a factor of 2 while even the best known molecule so far falls short of this limit by a factor of 30.