首页> 外文期刊>Russian Journal of General Chemistry >1,7-Dithioxo-Substituted Systems. Synthesis, Structure, and Photoconductivity of Bis(5,5-dimethyl-3-hydrazonocyclohex-1-enyl) Sulfide
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1,7-Dithioxo-Substituted Systems. Synthesis, Structure, and Photoconductivity of Bis(5,5-dimethyl-3-hydrazonocyclohex-1-enyl) Sulfide

机译:1,7-二硫代取代体系。双(5,5-二甲基-3-肼基环己基-1-烯基)硫化物的合成,结构和光电导性

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摘要

Bis(5,5-dimethyl-3-hydrazonocyclohex-1-enyl) sulfide was synthesized by the reaction of bis(5,5-dimethyl-3-thioxocyclohex-1-enyl) sulfide or its oxygen analog with hydrazine. Conformational lability of the molecule of dihydrazone was studied by the DFT(B3LYP) method using expanded basis sets 6-311G and 6-311G(d,p). Analysis of vibration IR and Raman spectra of the most stable conformers of the isolated molecule of dihydrazone was performed at the harmonic approximation. Using the Onsager SCRF solvation model the absence of solvent effect on the relative stability of the conformers was shown. The photoconductivity of dihydrazone was studied. Low value of the ratio of photocurrent to dark current (J_p/J_d = 2.5-3.5) for dyhydrazone was assigned to the lability of its stereoelectronic structure, which was in line with the data of ~1H, ~(13)C, and ~(15)N NMR spectra.
机译:通过双(5,5-二甲基-3-硫代环己基-1-烯基)硫化物或其氧类似物与肼的反应合成了双(5,5-二甲基-3-肼基环己基-1-烯基)硫化物。使用扩展的基础集6-311G和6-311G(d,p),通过DFT(B3LYP)方法研究了二hydr分子的构象不稳定性。在谐波近似下,对分离出的hydrhydr分子最稳定构象的振动红外光谱和拉曼光谱进行了分析。使用Onsager SCRF溶剂化模型显示,没有溶剂对构象异构体的相对稳定性产生影响。研究了hydr的光电导性。地hydr的光电流与暗电流之比的低值(J_p / J_d = 2.5-3.5)归因于其立体电子结构的不稳定性,这与〜1H,〜(13)C和〜的数据一致(15)N NMR光谱。

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