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孕酮的多晶型:从拓扑和实验压力-温度相图推断正交相I和II的相对稳定性。

Polymorphism of progesterone: relative stabilities of the orthorhombic phases I and II inferred from topological and experimental pressure-temperature phase diagrams.

作者信息

Barrio Maria, Espeau Philippe, Tamarit Josep Lluis, Perrin Marc-Antoine, Veglio Nestor, Ceolin René

机构信息

Laboratori de Caracterizació de Materials, Departament de Física i Enginyeria Nuclear, ETSEIB, Diagonal 647, 08028 Barcelona, Catalunya, Spain.

出版信息

J Pharm Sci. 2009 May;98(5):1657-70. doi: 10.1002/jps.21541.

Abstract

Temperatures and melting enthalpies of orthorhombic Phases I and II of natural progesterone, together with the temperature dependence of their lattice parameters and the specific volume of the melt at ordinary pressure, have been determined. With these results, a topological pressure-temperature (P-T) phase diagram accounting for the thermodynamic relationships between these phases has been constructed by way of the Clapeyron equation. The dependence of the melting temperature on the pressure has also been determined for each phase by high-pressure differential thermal analysis. It was found that, upon increasing the pressure, the melting curves converge to the I-II-liquid triple point (T(I-II-liquid) = 459.4 K, P(I-II-liquid) = 149.0 MPa), in close agreement with its topological location. This entails that Phase II should exhibit a stable phase region at higher pressure.

摘要

已测定了天然孕酮正交晶系I相和II相的温度、熔化焓,以及它们的晶格参数随温度的变化和常压下熔体的比容。利用这些结果,通过克拉佩龙方程构建了一个拓扑压力-温度(P-T)相图,该相图说明了这些相之间的热力学关系。还通过高压差热分析确定了每个相的熔化温度随压力的变化。结果发现,随着压力增加,熔化曲线汇聚到I-II-液相三相点(T(I-II-液相)= 459.4 K,P(I-II-液相)= 149.0 MPa),与其拓扑位置密切吻合。这意味着II相在更高压力下应呈现一个稳定相区。

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