Enantiomerically enriched, polycrystalline molecular sieves

被引:100
|
作者
Brand, Stephen K. [1 ]
Schmidt, Joel E. [1 ,2 ]
Deem, Michael W. [3 ,4 ]
Daeyaert, Frits [3 ,4 ]
Ma, Yanhang [5 ]
Terasaki, Osamu [5 ,6 ]
Orazov, Marat [1 ,7 ]
Davis, Mark E. [1 ]
机构
[1] CALTECH, Chem Engn, Pasadena, CA 91125 USA
[2] Univ Utrecht, Debye Inst Nanomat Sci, NL-3584 CG Utrecht, Netherlands
[3] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[4] Rice Univ, Dept Phys & Astron, Houston, TX 77005 USA
[5] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[6] Stockholm Univ, Dept Mat & Environm Chem, SE-10691 Stockholm, Sweden
[7] Stanford Univ, Chem Engn, Stanford, CA 94305 USA
关键词
chirality; zeolite; asymmetric catalysis; chiral adsorption; STRUCTURE-DIRECTING AGENTS; PURE-SILICA; ZEOLITE-BETA; ASYMMETRIC CATALYSIS; CHIRAL POLYMORPH; FACILE SYNTHESIS; CRYSTALLIZATION; CHALLENGES; COMPLEXES; FRAMEWORK;
D O I
10.1073/pnas.1704638114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Zeolite and zeolite-like molecular sieves are being used in a large number of applications such as adsorption and catalysis. Achievement of the long-standing goal of creating a chiral, polycrystalline molecular sieve with bulk enantioenrichment would enable these materials to perform enantioselective functions. Here, we report the synthesis of enantiomerically enriched samples of a molecular sieve. Enantiopure organic structure directing agents are designed with the assistance of computational methods and used to synthesize enantioenriched, polycrystalline molecular sieve samples of either enantiomer. Computational results correctly predicted which enantiomer is obtained, and enantiomeric enrichment is proven by high-resolution transmission electron microscopy. The enantioenriched and racemic samples of the molecular sieves are tested as adsorbents and heterogeneous catalysts. The enantioenriched molecular sieves show enantioselectivity for the ring opening reaction of epoxides and enantioselective adsorption of 2-butanol (the R enantiomer of the molecular sieve shows opposite and approximately equal enantioselectivity compared with the S enantiomer of the molecular sieve, whereas the racemic sample of the molecular sieve shows no enantioselectivity).
引用
收藏
页码:5101 / 5106
页数:6
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