Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan.
J Chem Phys. 2010 Mar 7;132(9):094107. doi: 10.1063/1.3332707.
Within the spin-unrestricted density functional theory (DFT) the long-range correction (LC) scheme combined with the Becke-Lee-Yang-Parr exchange-correlation functional, referred to as LC-UBLYP method, has been applied to the calculation of the second hyperpolarizability (gamma) of open-shell singlet diradical systems of increasing complexity and has demonstrated good performance: (i) for the simplest H(2) dissociation model, the gamma values calculated by the LC-UBLYP method significantly overshoot the full configuration interaction result but reproduce qualitatively the evolution of gamma as a function of the diradical character, (ii) for small singlet diradical 1,3-dipole systems, the diradical character dependence of gamma determined by the UCCSD and UCCSD(T) reference methods is reproduced semiquantitatively by the LC-UBLYP method except in the small diradical character region, where the spin-unrestricted solutions coincide with spin-restricted solutions, (iii) the LC-UBLYP method also closely reproduces the UCCSD(T) results on the diradical character dependence of gamma of the p-quinodimethane model system, particularly in the intermediate and large diradical character regions, whereas it shows an abrupt change for a diradical character (y) close to 0.2 originating from the triplet instability, (iv) the reliability of LC-UBLYP to reproduce reference coupled cluster results on open-shell singlet systems with intermediate and large diradical characters has also been substantiated in the case of gamma of 1,4-bis-(imidazol-2-ylidene)-cyclohexa-2,5-diene (BI2Y), then (v), for real systems built from a pair of phenalenyl radicals separated by a conjugated linker, the LC-UBLYP results have been found to closely match the UBHandHLYP values-which, for small systems are in good agreement with those obtained using correlated molecular orbital methods-whereas the UB3LYP results can be much different. These results are not only important from the viewpoint of an efficient determination of the nonlinear optical properties of open-shell singlet systems, but also from the viewpoint of defining new challenges for elaborating improved exchange-correlation functionals.
在无自旋限制密度泛函理论(DFT)中,结合 Becke-Lee-Yang-Parr 交换相关泛函的长程校正(LC)方案,称为 LC-UBLYP 方法,已被应用于计算复杂度不断增加的开壳单重态自由基体系的二阶超极化率(γ),并表现出良好的性能:(i)对于最简单的 H(2) 离解模型,LC-UBLYP 方法计算的γ值显著超过全组态相互作用结果,但定性地再现了 γ作为自由基特征函数的演化,(ii)对于小的单重态自由基 1,3-偶极体系,由 UCCSD 和 UCCSD(T)参考方法确定的γ的自由基特征依赖性由 LC-UBLYP 方法半定量再现,除了在小自由基特征区域,其中无自旋限制解与自旋限制解重合,(iii)LC-UBLYP 方法还紧密再现了 UCCSD(T) 关于 p-醌二甲基模型体系的γ的自由基特征依赖性的结果,特别是在中间和大自由基特征区域,而对于接近 0.2 的自由基特征(y),它表现出突然的变化,这源于三重态不稳定性,(iv)LC-UBLYP 方法在具有中间和大自由基特征的开壳单重态体系的γ上再现参考耦合簇结果的可靠性也在 1,4-双(咪唑-2-亚基)-环己-2,5-二烯(BI2Y)的情况下得到了证实,然后(v),对于由一对相隔共轭连接体的菲咯啉自由基构建的实际体系,LC-UBLYP 结果被发现与 UBHandHLYP 值非常匹配-对于小体系,与使用相关分子轨道方法获得的结果非常吻合-而 UB3LYP 结果可能大不相同。这些结果不仅从确定开壳单重态体系的非线性光学性质的有效方法的角度很重要,而且从定义改进交换相关泛函的新挑战的角度也很重要。