摘要
以两种手性氨基醇作为主体,运用1H NMR分别考察其对客体7个扁桃酸衍生物对映异构体的手性识别能力。结果表明,主客体物质的量之比为1∶1时,主体诱导客体对叔丁基扁桃酸消旋体最高产生37.6 Hz的化学位移差值。
The chiral recognition ability of these two chiral amino alcohols were evaluated as chiral solvating agent (host) for 7 mandelic acid derivatives enantiomers (guest) in the presence of an equimolar amount, respectively. As a result, the biggest chemical shift non-equivalences (△△δ) of 4-tert-butyl mandelic acid enantiomers induced by the two polydentate ligands was 37.6 Hz.
出处
《广州化学》
CAS
2012年第3期1-4,共4页
Guangzhou Chemistry
基金
国家大学生创新训练项目(AL11486)
中南大学研究生学位论文创新资助项目(2011xt083)
关键词
手性氨基醇
手性识别
扁桃酸衍生物
对映异构体
chiral amino alcohol
chiral recognition
mandelic acid derivatives
enantiomer