首页> 外文期刊>Russian Chemical Bulletin >Reactions of CH acids with the Michael acceptors in the presence of potassium carbonate 2*. Difluoroborines of 6-acetyl-2-cyclohexenones: synthesis, structure, and luminescence properties
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Reactions of CH acids with the Michael acceptors in the presence of potassium carbonate 2*. Difluoroborines of 6-acetyl-2-cyclohexenones: synthesis, structure, and luminescence properties

机译:Ch酸与迈克尔受体在碳酸钾2 *存在下反应。 6-乙酰基-2-环己酮的二氟硼杂硼:合成,结构和发光性能

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摘要

New 2-cyclohexenone derivatives were synthesized via the Michael reaction in the presence of potassium carbonate. These derivatives containing the acetyl substituent in position 6 are of special interest due to the ability to form boron chelate complexes, 1,3-dioxaborines, possessing luminescence properties. The dependence of the position of the absorption and luminescence absorption band maxima on the donor properties of the substituents was found.
机译:在碳酸钾存在下通过迈克尔反应合成新的2-环己酮衍生物。 由于能够形成硼螯合络合物,1,3-二氧化杂录,具有发光性能,含有第6位的乙酰基取代基的这些衍生物具有特殊兴趣。 发现了吸收和发光吸收带最大值对取代基供体性质的依赖性的依赖性。

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