In silico optimization of merocyanine-spiropyran compounds as second-order nonlinear optical molecular switches

Literature Information

Publication Date 2008-09-03
DOI 10.1039/B806561F
Impact Factor 3.676
Authors

Frédéric Castet, Laurent Ducasse, Jean-Luc Pozzo, Vincent Rodriguez


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Abstract

Time-dependent Hartree–Fock and Møller–Plesset second-order calculations have been used to unravel the relationships between structure and first hyperpolarizability in spiropyran/merocyanine couples and therefore to design efficient second-order nonlinear optical switching compounds. Large first hyperpolarizabilities for the merocyanine form as well as large contrasts of first hyperpolarizability have been obtained when, on the same species, (i) substituents at R1 and R2 positions on the phenolate ring of the merocyanine form are strong acceptor and donor substituents, respectively, (ii) the ethylenic bridge is substituted by donor groups, (iii) the other aromatic part of the system is benzimidazolo rather than indolino or benzothiazolo, and (iv) strong donor substituents are placed on the benzimidazolo moiety.

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Physical Chemistry Chemical Physics
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