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Imine-based [2]catenanes in water
Chemical Science ( IF 8.668 ) Pub Date : 2017-12-18 , DOI: 10.1039/C7SC04901C
Kenji Caprice, Marion Pupier, Anneli Kruve, Christoph A. Schalley, Fabien B. L. Cougnon

We report the efficient condensation of imine-based macrocycles from dialdehyde A and aliphatic diamines Bn in pure water. Within the libraries, we identified a family of homologous amphiphilic [2]catenanes, whose self-assembly is primarily driven by the hydrophobic effect. The length and odd-even character of the diamine alkyl linker dictate both the yield and the conformation of the [2]catenanes, whose particular thermodynamic stability further shifts the overall equilibrium in favour of imine condensation. These findings highlight the role played by solvophobic effects in the self-assembly of complex architectures.
更新日期:2018-01-31

 

Some contents have been Reproduced with permission of the American Chemical Society.
Some contents have been Reproduced by permission of The Royal Society of Chemistry.
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