The origin of dramatic variation in optical polarizabilities of push–pull conjugated chains with respect to the conjugation length is discussed. Ab initio calculations of intramolecular charge transfer (ICT)-driven dipole moment (μCT), polarizability (αCT), and first hyperpolarizability (βCT) show that the values of αCT/μCT and βCT/μCT change linearly and quadratically with respect to the conjugation length, respectively. The maximum ICT-driven coherence sizes of αCT and βCT are consistent with the time-dependent densities to the first (ρ(1)) and second (ρ(2)) orders of the electric field obtained from the collective electronic oscillators method.
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Lee et al. (2003) studied this question.
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