乙烯的第二超极化性

B. Champagne, T. Kubo, Hideaki Takahashi, M. Nakano, A. Takebe, Masahito Nate, E. Botek, K. Kamada, R. Kishi, K. Ohta
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引用次数: 56

摘要

利用UBHandHLYP杂化密度泛函理论方法研究了乙烯的静态二阶超极化率(γ)。虽然乙烯最初被认为是闭壳体系,但根据不受自旋限制的Hartree-Fock自然轨道(UNOs)的占据数计算其双自由基性质值,表明其具有开壳双自由基性质,并且随着中环区域的大小而增加,因为该区域的芳构性得到恢复。作为参考,我们还研究了四苯并多烯的γ值,由于其可忽略不计的双自由基特性,它们被认为是相应的闭壳体系。研究发现,乙烯的纵向γ值远大于相应的参考闭壳体系,而其比值γ(乙烯)/γ(参考)随中间环区域长度的增加而减小,即随双自由基性质的增加而减小。
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Second Hyperpolarizability of Zethrenes
We report a study on the static second hyperpolarizabilities (γ) of zethrenes using the UBHandHLYP hybrid density functional theory method. Though zethrenes were originally considered as closed-shell systems, the values of their diradical characters, calculated from the occupation numbers of spin-unrestricted Hartree-Fock natural orbitals (UNOs), demonstrate an open-shell diradical nature, which increases with the size of the middle ring region because of the recovery of the aromaticity in that region. As references, we examine also the γ values of tetrabenzopolyacenes, which are regarded as the corresponding closed-shell systems due to their negligible diradical characters. It is found that the longitudinal γ values for zethrenes are much larger than those of the corresponding reference closed-shell systems, whereas their ratio, γ(zethrene)/γ(reference), is reduced when increasing the length of middle ring regions, i.e., when increasing the diradical character.
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