کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1323040 | 1499919 | 2012 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Quantum chemical study on first hyperpolarizabilities of mono- and bimetal Pt(II) diimine complexes Quantum chemical study on first hyperpolarizabilities of mono- and bimetal Pt(II) diimine complexes](/preview/png/1323040.png)
The static first hyperpolarizabilities (βvec) of ligand L (N,N′-bis(4-methoxyphenyl)ethylenediimine) and its Pt(II) chelated complexes have been calculated by density functional theory (DFT) method. The results show that the βvec values of Pt(II) diimine complexes range from ∼4.2 to ∼198.8 times larger than that of ligand L, and the βvec values of Pt(II) complexes with coordinated atom O are larger than those of the corresponding complexes with S. Notably, the bimetallic complex 3a possesses the largest βvec value in the studied systems, ∼1498.86 × 10−30 esu, which is ∼46.6, ∼30.5, and ∼3.6 times as large as those of complexes 1a, 2a and 3b, respectively. In addition, the dynamic first hyperpolarizabilities (βvec(ω)) of complex 1a are also calculated at the input photon energy from 0.1 to 1.8 eV. Our present work would be beneficial for further theoretical and experimental studies on large second-order nonlinear optical (NLO) responses of metal complexes.
The second-order nonlinear optical (NLO) properties on ligand L (N,N′-bis(4-methoxyphenyl)ethylenediimine) and its Pt(II) chelated complexes have been calculated by density functional theory (DFT) method. The static first hyperpolarizabilities (βvec) of the studied systems increase obviously with the increasing the π-conjugated groups and the number of Pt(II).Figure optionsDownload as PowerPoint slideHighlights
► βvec value increases with the increasing π-conjugated groups and the number of Pt(II).
► Coordinated atom (X = O, S) affects the βvec values of the studied complexes.
► βvec(ω) value of complex 1a can be measured at the region ranging from 0.0 to 0.7 eV.
Journal: Journal of Organometallic Chemistry - Volume 718, 1 November 2012, Pages 1–7