Abstract
Molecular switches, rotors, and motors play an important role in the development of nano-machines and devices, as well as responsive and adaptive functional materials. For unidirectional rotors based on chiral overcrowded alkenes, their stereochemical homogeneity is of crucial importance. Herein, a method to obtain new and functionalizable overcrowded alkenes in enantiopure form is presented. The procedure involves a short synthesis of three steps and a solvent-switchable chiral resolution by using a readily available resolving agent. X-ray crystallography revealed the mode of binding of the motor with the resolving agent, as well as the absolute configuration of the motor. H-1 NMR and UV/Vis spectroscopy techniques were used to determine the dynamic behavior of this molecular motor. This method provides rapid access to ample amounts of enantiopure molecular motors, which will greatly facilitate the further development of responsive molecular systems based on chiral overcrowded alkenes.
Original language | English |
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Pages (from-to) | 7054-7058 |
Number of pages | 5 |
Journal | Chemistry |
Volume | 22 |
Issue number | 21 |
DOIs | |
Publication status | Published - 17-May-2016 |
Keywords
- chirality
- conformation analysis
- resolution
- solvent effects
- DIELECTRICALLY CONTROLLED RESOLUTION
- SINGLE RESOLVING AGENT
- OPTICAL RESOLUTION
- EFFICIENT RESOLUTION
- PHOSPHATE-BINDING
- SOLVENT
- LIGHT
- MACHINES
- ACID
- MECHANISM
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CCDC 1452497: Experimental Crystal Structure Determination
Leeuwen ,van, T. (Contributor), Gan, J. (Contributor), Kistemaker, J. (Contributor), Pizzolato, S. (Contributor), Chang, M.-C. (Contributor) & Feringa, B. L. (Contributor), University of Groningen, 10-Feb-2016
DOI: 10.5517/ccdc.csd.cc1krfrh
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