首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Selective Formation and SHG Intensity of Noncentrosymmetric and Centrosymmetric 1,1,2,2-Tetramethyl-1-(4-(N,N-dimethylamino)phenyl)-2-(2 '-cyanophenyl)disilane Crystals under External Stimuli
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Selective Formation and SHG Intensity of Noncentrosymmetric and Centrosymmetric 1,1,2,2-Tetramethyl-1-(4-(N,N-dimethylamino)phenyl)-2-(2 '-cyanophenyl)disilane Crystals under External Stimuli

机译:在外部刺激下,选择性形成和非致白二元和亚苯二甲苯基-1-(4-(N,N-二甲基氨基)苯基)-2-(2'-苯基苯基)苯二硅烷晶体下的无苯二酚和亚苯二甲酸苯基-1-(4-(N,2'-氰基苯基)苯胺晶体

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摘要

In this paper, selective formation of noncentrosymmetric (Cc; alpha-crystal) and centrosymmetric (P2(1)/c; beta-crystal) 1,1,2,2-tetramethyl-1-(4-(N,N-dimethylamino)phenyl)-2-(2'-cyanophenyl)disilane (1) was reported and both crystals were characterized by single-crystal X-ray diffraction (XRD) analysis, indicating multiple CH-pi interactions created the crystal packing. The second harmonic generation (SHG) activity was attributed to the crystal packing and the orientation of dipole moment. Noncentrosymmetric crystal packing in a parallel manner exhibited SHG activity (intensity: 2.1 times vs urea). On the contrary, centrosymmetric structure in an antiparallel form showed no SHG activity (intensity: 0.0 times vs urea). As the calculated crystal energies of two polymorphs were very close to each other, the regulation of alpha- and beta-crystals is succeeded through supercooled liquid-to-crystal and crystal-to-crystal phase transitions, controlling the SHG activity. Powder XRD and solid-state C-13 NMR spectroscopy were applied for the qualitative analysis of alpha- or beta-polymorphs.
机译:在本文中,选择性地形成非浓对称(CC;α晶体)和亚里索对称(P2(1)/ c;β-晶体)1,1,2,2-四甲基-1-(4-(N,N-二甲基氨基报道,苯基)-2-(2'-氰基苯基)二硅烷(1),并通过单晶X射线衍射(XRD)分析表征两种晶体,表明多个CH-PI相互作用产生了晶体填料。第二次谐波产生(SHG)活性归因于晶体填料和偶极矩的方向。非胞间对称晶体包装以平行方式表现出SHG活性(强度:2.1次VS尿素)。相反,处于反平行形式的亚烃结构显示出SHG活性(强度:0.0倍,尿素)。随着两个多晶型物的计算晶体能量彼此非常靠近,作为α-和β-晶体的调节通过过冷液 - 晶体和晶体 - 晶相转变,控制SHG活性。粉末XRD和固态C-13 NMR光谱施用于α-或β-多晶型物的定性分析。

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