The open-shell character dependences of the second hyperpolarizability, γ, are investigated for rectangular-shaped tetraradicaloid models, such as diradical dimers, using numerically exact solutions of the extended Hubbard model. The newly defined local diradical characters for intra- and intermolecular interactions (referred to as y intra and y inter, respectively) are compared to conventional global ones ( y 0 and y 1 ) and provide a comprehensive understanding of the electronic structure of the system. The system shows two kinds of enhancements of the γ components, γ intra and γ inter (caused, respectively, by intra- and intermolecular diradical interactions): (i) a system with a large y intra ( y inter ) (>∼0.4) exhibits the enhancement of a single component of γ, γ inter (γ intra ), at the intermediate y inter ( y intra ) region (∼0.3–0.4), and (ii) in contrast to conventional diradical systems, the system exhibits a further enhancement of both components of γ (γ intra and γ inter ) at the region where y intra ∼ y inter with small values (≤∼0.3). The obtained relationships are verified by using ab initio quantum chemical calculations of the realistic tertraradical models of a 4,4′-bis(1,2,3,5-dithiazdiazolyl) (BDTDA) dimer and a disilene dimer. The present results are expected to pioneer an alternative class of two-dimensional multiradical NLO systems, which potentially cause further enhancement of γ as compared with conventional intermediate diradical NLO systems.
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Matsui et al. (2018) studied this question.
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