Structural analysis of two foldamer-type oligoamides the effect of hydrogen bonding on solvate formation, crystal structures and molecular conformation
Suhonen, A., Nauha, E., Salorinne, K., Helttunen, K., & Nissinen, M. (2012). Structural analysis of two foldamer-type oligoamides – the effect of hydrogen bonding on solvate formation, crystal structures and molecular conformation. CrystEngComm, 14 (21), 7398-7407. doi:10.1039/c2ce25981h Retrieved from http://pubs.rsc.org/en/content/articlelanding/2012/ce/c2ce25981h#!divA...
© Royal Society of Chemistry. This is an author's final draft version of an article whose final and definitive form has been published by RSC.
The crystal structures and molecular conformations of two foldamer-type oligoamides were analyzed. One polymorphic form and seven solvates were found for N¹,N³-bis(2-benzamidophenyl)benzene-1,3-dicarboxamide (the benzene variant), and two polymorphic forms and six solvates for N²,N⁶-bis(2-benzamidophenyl)pyridine-2,6-dicarboxamide (the pyridine variant). Three crystal structures of the benzene variant and seven structures of the pyridine variant were solved using single crystal X-ray diffraction. The crystal structures showed that the different modes of intramolecular hydrogen bonding strongly affect the conformation and folding of the molecules, which is most evidently seen with the strongly folded helical structure of the pyridine variant. NOESY experiments suggest that the intramolecular hydrogen bonding is stable enough to retain a folded or partially folded conformation even in solution.
Author's Final draft