首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >PROPERTIES OF THE KETO AMIDES FORMED BY AMINOLYSIS OF 3,7-DIARYLPYRANO[4,3-c]PYRAN-l,5-DIONE DERIVATIVES:A SOLID-STATE REACTION,CRYSTAL STRUCTURES,AND THERMAL ANALYSIS
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PROPERTIES OF THE KETO AMIDES FORMED BY AMINOLYSIS OF 3,7-DIARYLPYRANO[4,3-c]PYRAN-l,5-DIONE DERIVATIVES:A SOLID-STATE REACTION,CRYSTAL STRUCTURES,AND THERMAL ANALYSIS

机译:通过3,7-二芳基吡喃并[4,3-c]吡喃-1,5-二酮衍生物的胺化反应制得的酮基酰胺:固相反应,晶体结构和热分析

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摘要

Aminolysis of 3,7-diarylpyrano[4,3-c]pyran-l,5-dione derivatives gave keto amides,which upon heating returned back to the original compounds in the solid state.X-Ray crystallographic analysis of the keto amides showed proximate orientations of the ketone and the amide groups.TGA and DTA of the keto amides clarified a kind of solid-state reaction which occurred in appearance without melting,but microscopically proceeded via melting of the keto amides,structural change,and crystallization of the products.
机译:对3,7-二芳基吡喃并[4,3-c]吡喃-1,5-二酮衍生物进行氨解反应,得到酮酰胺,加热后又回到固态,回到原来的化合物。X-射线晶体学分析酮酰胺酮酰胺的TGA和DTA澄清了一种固态反应,该反应在外观上没有熔化,但在微观上通过酮酰胺的熔化,结构变化和产物结晶而进行。 。

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