化学
部分
氢键
互变异构体
超分子化学
光化学
烯醇
结构母题
二芳基乙烯
芳香性
结晶学
立体化学
光致变色
分子
催化作用
晶体结构
有机化学
生物化学
作者
Bohan Tang,Mike Pauls,Christoph Bannwarth,Stefan Hecht
摘要
Multiple hydrogen-bonding motifs serve as important building blocks for molecular recognition and self-assembly. Herein, a photoswitchable quadruple hydrogen-bonding motif featuring near-complete, reversible, and thermostable conversion between DADA and AADD arrays associated with an alteration of their dimerization constants by over 3 orders of magnitude is reported. The system is based on a diarylethene featuring a ureidopyrimidin-4-ol moiety, which upon photoinduced ring closure and associated loss of aromaticity undergoes enol-keto tautomerization to a ureidopyrimidinone moiety. The latter causes a transformation of the hydrogen-bonding arrays and significantly weakens the free energy of dimerization in the case of the closed isomer. This photoswitchable quadruple hydrogen-bonding motif should allow us to spatially and temporarily direct self-assembly and supramolecular polymerization processes by light.
科研通智能强力驱动
Strongly Powered by AbleSci AI