© Springer Science+Business Media Dordrecht 2015. The synthesis of a C4 dissymmetric resorcinarene tetracarboxylic acid derivative and determination of its critical micelle concentration is reported. The tetrahydroxy derivative was prepared by reduction of the tetra-acid. The low-temperature single crystal X-ray structure of the methyl ester derivative of the tetra-acid is also reported. This crystallised with two independent molecules of similar boat (flattened cone) conformation within the asymmetric unit.
|Journal||Journal of Inclusion Phenomena and Macrocyclic Chemistry|
|Publication status||Published - 2015|
Mcildowie, M. J., Mocerino, M., Ogden, M. I., Skelton, B., & White, A. (2015). C4 dissymmetric resorcinarene derivatives: Synthesis, crystal structure and micelle formation. Journal of Inclusion Phenomena and Macrocyclic Chemistry, 82(1), 47-51. https://doi.org/10.1007/s10847-015-0525-8