首页> 外文期刊>International Journal of Quantum Chemistry >Diradicalology in third-order nonlinear optical systems: Second hyperpolarizabilities of acetylene-linked phenalenyl-based superpolyenes
【24h】

Diradicalology in third-order nonlinear optical systems: Second hyperpolarizabilities of acetylene-linked phenalenyl-based superpolyenes

机译:三阶非线性光学系统的径向动力学:乙炔基连接的基于菲基的超多烯的第二超极化率

获取原文
获取原文并翻译 | 示例
       

摘要

From the viewpoint of "diradical character," referred to as "diradicalology," we investigate the second hyperpolarizability γ - the molecular third-order nonlinear optical (NLO) property - of one-dimensional supermolecular systems composed of acetylene-linked phenalenyl/pyrene rings using long-range corrected spin-unrestricted density functional theory. It turns out that the pyrene-based superpolyenes (Py-n) behave like closed-shell systems, whereas phenalenyl-based superpolyenes (Ph1-n and Ph2-n) have different diradical characters depending on the linked form, that is, Ph1-n and Ph2-n have intermediate and pure diradical characters, respectively. In comparison with Py-n and Ph2-n, the longitudinal γ of Ph1-n is significantly larger, and it displays larger enhancement as a function of system size. Substitutions to the terminal rings by donor (NH_2) and acceptor (NO_2) groups further enhance γ in Ph1-n, more than in Ph2-n and Py-n. These results are in agreement with the structure-property relationships derived for open-shell NLO systems with symmetric and asymmetric charge distributions (Nakano et al., J. Chem. Phys. 2010, 133, 154302).
机译:从“双自由基性”(称为“双自由基性”)的角度,我们研究由乙炔键合的苯撑/ py环组成的一维超分子系统的第二超极化率γ(分子三阶非线性光学(NLO)性质)使用远程校正自旋无限制密度泛函理论。事实证明,pyr基超多烯(Py-n)的行为类似于闭壳系统,而苯环基基超多烯(Ph1-n和Ph2-n)根据连接形式(即Ph1-n)具有不同的双自由基特征n和Ph2-n分别具有中间和纯双自由基特征。与Py-n和Ph2-n相比,Ph1-n的纵向γ明显更大,并且随着系统大小的变化,其显示出更大的增强。供体(NH_2)和受体(NO_2)基团取代末端环后,Ph1-n中的γ进一步增强,而Ph2-n和Py-n中的γ增强更多。这些结果与具有对称和不对称电荷分布的开壳NLO系统的结构-性质关系一致(Nakano等人,J.Chem.Phys.2010,133,154302)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号