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Tuning First Molecular Hyperpolarizabilities through the Use of Proaromatic Spacers

2005; American Chemical Society; Volume: 127; Issue: 24 Linguagem: Inglês

10.1021/ja051819l

1943-2984

Raquel Andreu, María‐Jesús Blesa, Laura Carrasquer, Javier Garı́n, J. Orduna, Belén Villacampa, R. Alcalá, Juan Casado, M. Carmen Ruiz Delgado, Juan T. López Navarrete, Magali Allain,

Electron Spin Resonance Studies

In this paper, we describe the second-order nonlinear optical properties of a series of 1,3-dithiole-based electron donor−acceptor systems incorporating proaromatic donor and spacer groups. Modification of the proaromaticity of the quinoid spacer gives rise to NLO-phores with μβ values ranging from −2000 × 10-48 esu to +3000 × 10-48 esu. Quite surprisingly, compounds with a p-benzoquinoid spacer and a strong acceptor group show negative μβ values, usually associated to zwitterionic ground states, and yet they are largely quinoid, as evidenced by crystallographic data and theoretical calculations. Progressive benzoannulation of the spacer and introduction of alkylsulfanyl substituents on the dithiole donor unit result in a shift to more positive μβ values. DFT and ab initio calculations verify these empirical trends.