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分子晶体的固溶强化:奥美拉唑的互变异构多晶型物。

Solid solution hardening of molecular crystals: tautomeric polymorphs of omeprazole.

机构信息

Solid State and Structural Chemistry Unit, Indian Institute of Science , Bangalore 560 012, India.

出版信息

J Am Chem Soc. 2015 Feb 11;137(5):1794-7. doi: 10.1021/ja512817f. Epub 2015 Feb 2.

Abstract

In the context of processing of molecular solids, especially pharmaceuticals, hardness is an important property that often determines the manufacturing steps employed. Through nanoindentation studies on a series of omeprazole polymorphs, in which the proportions of the 5- and 6-methoxy tautomers vary systematically, we demonstrate that solid-solution strengthening can be effectively employed to engineer the hardness of organic solids. High hardness can be attained by increasing lattice resistance to shear sliding of molecular layers during plastic deformation.

摘要

在分子固体(特别是药物)的加工过程中,硬度是一个重要的性质,通常决定了所采用的制造步骤。通过对一系列奥美拉唑多晶型物的纳米压痕研究,其中 5- 和 6-甲氧基互变异构体的比例系统地变化,我们证明可以有效地利用固溶强化来设计有机固体的硬度。通过增加晶格对分子层在塑性变形过程中剪切滑移的阻力,可以获得高硬度。

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