Controlling Molecular Isomerization by Water

Controlling Molecular Isomerization by Water

Donor-acceptor Stenhouse adducts (DASAs) are attractive for the reversible visible light/heat-induced linear-cyclic isomerization, which have been widely applied in light-controlled drug delivery, surface wetting and self-assembly. However, since they were firstly synthesized by Read de Alaniz’s group in 2014, DASAs were mostly used as photoresponsive molecules. Read de Alaniz’s group focused on the chemical modification and triggered light shifting of DASAs, while another famous group from Netherland, Feringa’s group focused on the mechanism during light-induced linear-to-cyclic isomerization. 

I have been interested in DASAs since I was a Ph.D student in Max-Planck-Institute for Polymer Research in 2015, where I was focused on red-light-responsive supramolecular interactions between azobenzene and cyclodextrin. The host-guest complexes responsive to long-wavelength-light are potential to be applied in biomedical field. 

Therefore, after back to China, I decided to work on DASAs. There was one day, I accidentally added one drop of water into the toluene solution of DASA-N, and then lock the mixture into my draw (Figure). Interestingly, I found the purple linear DASA-N solution faded the next morning (Figure). Then we noticed that this phenomenon (water-induced linear-to-cyclic isomerization of DASAs) was also reported by Read de Alaniz’s group and Feringa’s group, however, both of them did not investigate the mechanism and reversibility. 

The water-induced linear-to-cyclic isomerization was demonstrated to be a thermal process, that is, cyclic DASAs are stabilized by water molecules. These were further demonstrated by density functional theory (DFT) and molecular dynamic (MD) simulations. DASAs can coordinate with water molecules to form DASAs·xH2O, which further lower the molecular energy of cyclic DASAs. After that we were thinking, is the water-induced linear-to-cyclic isomerization reversible? Then we tried to remove the coordinated water molecules. We tried anhydrous MgSO4 and microwave oven, which did not work. Then after guiding of thermogravimetric analysis, cyclic DASAs·xH2O was heated under 180 oC, which triggered the coordinated water molecules loss and further induced cyclic-to-linear isomerization. This makes DASAs to be applied in information hiding/displaying on paper and color-switching inks. 

Therefore, DASAs are not only photoresponsive molecules. This research broadens the investigations and applications of DASAs. It also makes me to rethink the other well-known photoresponsive molecules, including azobenzene, spiropyran et al. Actually, we are still focusing on the mechanism and more applications on the reversible water-induced linear-cyclic isomerization of DASAs. Please keep paying attention to our followed works. 

Please read our paper for the full story. 


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