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Updated: Apr 20, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Theoretical study on the relationship between diradical character and second hyperpolarizabilities of
Hiroshi Matsui1, Kotaro Fukuda, Shota Takamuku
1Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531 (Japan).
Abstract:
By using spin-unrestricted density functional theory methods, the relationship between the diradical character y and the second hyperpolarizability γ (the third-order nonlinear optical (NLO) properties at the molecular scale) for four-membered-ring diradical compounds, that is, cyclobutane-1,3-diyl, Niecke-type diradicals, and Bertrand-type diradicals, were investigated by focusing on the substitution effects of heavy main-group elements as well as of donor/acceptor groups on the y and γ values. It has been found that i) γ is enhanced in the intermediate y region for these four-membered-ring diradicals, ii) Niecke-type diradicals with intermediate y values, which are realized by tuning the combination of the main-group elements involved, exhibit larger γ values than Bertrand-type diradicals, and iii) the y value and thus γ value can be controlled by modifying the both-end donor/acceptor substituents attached to carbon atoms in Nicke-type C2 P2 diradicals. These results demonstrate that four-membered-ring diradicals involving heavy main-group elements exhibit high controllability of the y and γ, which indicates the potential applications of four-membered-ring diradicals as a building block of highly efficient open-shell NLO materials.
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