Durand Raphaël J, Achelle Sylvain, Robin-Le Guen Françoise, Caytan Elsa, Le Poul Nicolas, Barsella Alberto, Guevara Level Patricia, Jacquemin Denis, Gauthier Sébastien
Univ. Rennes, CNRS, ISCR (Institut des Sciences Chimiques de Rennes) - UMR 6226, F-35000 Rennes, France.
Dalton Trans. 2021 Apr 7;50(13):4623-4633. doi: 10.1039/d1dt00151e. Epub 2021 Mar 12.
A series of four D-(π-Pt-π-A) new V-shaped binuclear platinum(ii) complexes bearing a diphenylpyranylidene ligand as a pro-aromatic donor group (D) and various electron-attracting groups (A) separated by platinum bis-acetylide fragments have been synthesized, characterized and studied for their electrochemical, photophysical and second-order nonlinear optical (NLO) properties. The nonlinear optical properties of these complexes have been determined by using the Electric-Field-Induced Second Harmonic (EFISH) generation technique, and their optical properties have been rationalized by Time-Dependent Density Functional Theory (TD-DFT) calculations relying on a range-separated hybrid. All complexes display positive μβ values. In addition, the second-order NLO responses of the complexes could be easily modulated by incorporating various end-capped electron-attracting groups, namely malononitrile, indane-1,3-dione, pyrimidine and pyrimidinium. Remarkably, complex 7 bearing a pyrimidinium fragment displays the highest μβ value among all the complexes of this series. Its NLO response is twice as high as that of the mononuclear analogue complex RD2, which has been confirmed both experimentally and theoretically.
合成了一系列四个D-(π-Pt-π-A)新型V形双核铂(II)配合物,其带有二苯基吡喃亚甲基配体作为前芳香供体基团(D)以及由铂双乙炔片段隔开的各种吸电子基团(A),对其进行了表征,并研究了它们的电化学、光物理和二阶非线性光学(NLO)性质。这些配合物的非线性光学性质通过电场诱导二次谐波(EFISH)产生技术测定,其光学性质通过基于范围分离杂化的含时密度泛函理论(TD-DFT)计算进行了合理化分析。所有配合物均显示出正的μβ值。此外,通过引入各种封端吸电子基团,即丙二腈、茚满-1,3-二酮、嘧啶和嘧啶鎓,可轻松调节配合物的二阶NLO响应。值得注意的是,带有嘧啶鎓片段的配合物7在该系列所有配合物中显示出最高的μβ值。其实验和理论均证实,其NLO响应是单核类似配合物RD2的两倍。