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通过高内相乳液法由手性螺旋取代聚乙炔构建的光学活性多孔材料及其在对映选择性结晶中的应用。

Optically Active Porous Materials Constructed by Chirally Helical Substituted Polyacetylene through a High Internal Phase Emulsion Approach and the Application in Enantioselective Crystallization.

作者信息

Liang Junya, Wu Yi, Deng Xuesheng, Deng Jianping

机构信息

State Key Laboratory of Chemical Resource Engineering and College of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

出版信息

ACS Macro Lett. 2015 Oct 20;4(10):1179-1183. doi: 10.1021/acsmacrolett.5b00613. Epub 2015 Oct 8.

Abstract

This article reports the first optically active macroporous materials constructed by helical substituted polyacetylene and prepared by a high internal phase emulsion (HIPE) technique. The macroporous (∼3 μm) materials were fabricated simply through polymerization of the continuous phase in HIPEs. The porous structures of the resulting materials can be adjusted by varying the fraction of the dispersed phase. The obtained materials were characterized by regular pore morphology, high porosity, and low density. Circular dichroism and UV-vis absorption spectra demonstrated that the substituted polyacetylene forming the materials adopted chirally helical conformations, which endowed the materials with considerable optical activity. The optically active porous materials were used as chiral inducers and efficiently induced enantioselective crystallization of threonine and alanine racemates. l-Threonine and l-alanine were preferably induced to form crystals from the respective racemic solutions. The prepared materials open a new type of functional chiral materials with potential applications in asymmetric catalysis, chiral resolution, etc.

摘要

本文报道了首例由螺旋取代聚乙炔构建并通过高内相乳液(HIPE)技术制备的光学活性大孔材料。大孔(约3μm)材料通过在高内相乳液中连续相的聚合简单制备而成。所得材料的多孔结构可通过改变分散相的比例进行调节。所获得的材料具有规则的孔形态、高孔隙率和低密度。圆二色光谱和紫外可见吸收光谱表明,形成材料的取代聚乙炔采用手性螺旋构象,赋予材料显著的光学活性。该光学活性多孔材料用作手性诱导剂,有效诱导苏氨酸和丙氨酸外消旋体的对映选择性结晶。L-苏氨酸和L-丙氨酸更倾向于从各自的外消旋溶液中诱导形成晶体。所制备的材料开辟了一种新型功能性手性材料在不对称催化、手性拆分等方面具有潜在应用。

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