Conformational changes in Cmethyl-resorcinarene pyridine N-oxide inclusion complexes in the solid state
Puttreddy, R., Beyeh, N. K., & Rissanen, K. (2016). Conformational changes in Cmethyl-resorcinarene pyridine N-oxide inclusion complexes in the solid state. CrystEngComm, 18 (26), 4971-4976. doi:10.1039/C6CE00240D
© the Authors, 2016. This is an open access article published by RSC. Licensed under a Creative Commons Attribution 3.0 Unported Licence.
Aromatic N-oxides interact with Cmethyl-resorcinarene resulting in marked changes in the conformation of the host resorcinarene. In the solid state, 2- and 3-methylpyridine N-oxides form pseudo-capsular 2 : 2 endo host–guest complexes with Cmethyl-resorcinarene stabilized by C–H⋯π interactions. The Cmethylresorcinarene·2-methylpyridine N-oxide complex has a C4v crown conformation, while the Cmethylresorcinarene·3-methylpyridine N-oxide complex has a slightly open C2v boat conformation. On the contrary, other para-substituted and benzo-fused pyridine N-oxides form only exo complexes with Cmethyl-resorcinarene. In the exo complexes, the asymmetry of the guest, conformational flexibility and preferred inter-host hydrogen bonding of Cmethyl-resorcinarenes exclude endo complexation. All the exo complexes form robust 1-D hydrogen bonded chains between the host hydroxyl groups assisted by the guest N–O groups, resulting in a C2v boat conformation.