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首页> 外文期刊>Theoretical chemistry accounts >Cis-trans isomerization and spin multiplicity dependences on the static first hyperpolarizability for the two-alkali-metal- doped saddle[4]pyrrole compounds
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Cis-trans isomerization and spin multiplicity dependences on the static first hyperpolarizability for the two-alkali-metal- doped saddle[4]pyrrole compounds

机译:顺式-反式异构化和自旋多重性对两碱金属掺杂的马鞍[4]吡咯化合物的静态第一超极化率的依赖性

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摘要

Doping two alkali-metal atoms (Li and Na) into the saddle-shaped saddle[4]pyrrole forms four new two-alkali-metal-doped compounds with alkalide or electride characteristic. They are cis-LiNa(saddle[4]pyrrole) isomers l(singlet) and 2(triplet), and trans-Li(saddle[4]pyrrole)Na isomers 3(singlet) and 4(triplet). The four structures with all-real frequencies are obtained at the density functional theory (DFT) B3LYP/6-311+G(d) level. All calculations of electric properties have been carried out at the second order M0ller-Plesset perturbation theory (MP2) level. The order of the β0 values is 3.54 x 10~3 for trans-4(triplet) <1.51 x 10~4 for cis-1(singlet)<3.57 x 10~4 for cis-2(triplet)<2.34 x 10~5 a.u. for trans-3(singlet). The static first hyperpolarizability (β0) depends on the cis-trans isomerization and spin multiplicity. The result demonstrates that the cis-trans isomerization and spin multiplicity controls of the second-order NLO response are possible.
机译:将两个碱金属原子(Li和Na)掺杂到马鞍形马鞍[4]吡咯中可形成四个具有碱金属或电子特征的新的两碱金属掺杂化合物。它们是顺式-LiNa(马鞍[4]吡咯)异构体1(三重链)和反式-Li(马鞍[4]吡咯)Na异构体3(重链)和4(三重链)。在密度泛函理论(DFT)B3LYP / 6-311 + G(d)级别获得了具有全实频率的四个结构。电性能的所有计算均在二阶Molller-Plesset微扰理论(MP2)级别进行。对于trans-4(三胞胎),β0值的顺序为3.54 x 10〜3;对于cis-1(三胞胎),<1.51 x 10〜4为<3.57 x 10〜4对于顺式2(三胞胎)<2.34 x 10〜 5金对于trans-3(单个)。静态第一超极化率(β0)取决于顺反异构化和自旋多重性。结果表明,二阶NLO响应的顺反异构化和自旋多重性控制是可能的。

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