Asymmetric autocatalysis triggered by triglycine sulfate with switchable chirality by altering the direction of the applied electric field

被引:7
|
作者
Kawasaki, Tsuneomi [1 ]
Kaimori, Yoshiyasu [1 ]
Shimada, Seiya [1 ]
Hara, Natsuki [1 ]
Sato, Susumu [1 ]
Suzuki, Kenta [1 ]
Asahi, Toru [2 ]
Matsumoto, Arimasa [1 ,4 ]
Soai, Kenso [1 ,3 ]
机构
[1] Tokyo Univ Sci, Dept Appl Chem, Shinjuku Ku, Tokyo 1628601, Japan
[2] Waseda Univ TWIns, Dept Life Sci & Med Biosci, Shinjuku Ku, Wakamatsu Cho, Tokyo 1628480, Japan
[3] Waseda Univ, Res Org Nano & Life Innovat, Shinjuku Ku, Wasedatsurumaki Cho, Tokyo 1620041, Japan
[4] Nara Womens Univ, Dept Chem Biol & Environm Sci, Kita Uoya Nishi Machi, Nara 6308506, Japan
基金
日本学术振兴会;
关键词
CIRCULARLY-POLARIZED-LIGHT; SYMMETRY-BREAKING; ENANTIOSELECTIVE SYNTHESIS; GLYCINE SULFATE; AMPLIFICATION; MOLECULES; MECHANISM; PHASE; QUANTIFICATION; HOMOCHIRALITY;
D O I
10.1039/d1cc02162a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Triglycine sulfate (TGS) acts as a chiral trigger for asymmetric autocatalysis with amplification of enantiomeric excess, i.e., the Soai reaction. Therefore, molecular chirality of highly enantioenriched organic compounds is controlled by a ferroelectric crystal TGS, whose polarization is altered by an electric field.
引用
收藏
页码:5999 / 6002
页数:4
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