异构化
立体选择性
化学
对映体
滴定法
立体化学
磷酸盐
基质(水族馆)
螺旋度
离子
核磁共振波谱
立体异构
分子
物理化学
催化作用
有机化学
地质学
海洋学
物理
粒子物理学
作者
Matea Vlatković,Ben L. Feringa,Sander J. Wezenberg
标识
DOI:10.1002/anie.201509479
摘要
A chiral bisurea anion receptor, derived from a first-generation molecular motor, can undergo photochemical and thermal isomerization operating as a reconfigurable system. The two possible cis configurations in the isomerization cycle are opposite in helicity, as is shown by CD spectroscopy. (1)H NMR titrations demonstrate that the P and M helical cis isomers hold opposite enantioselectivity in the binding of binol phosphate, while anion complexation by the intermediate trans isomer is not selective. The difference in the binding affinity of the enantiomers was rationalized by DFT calculations, revealing very distinct binding modes. Thus, the enantiopreferred substrate binding in this receptor can be inverted in a dynamic fashion using light and heat.
科研通智能强力驱动
Strongly Powered by AbleSci AI