Conformational diversity and dynamics of distally disubstituted calix and thiacalix[4]arenes in solution. (4th April 2013)

• Record Type: Journal Article
• Authors: Latypov, Shamil K.; Kharlamov, Sergey V.; Muravev, Anton A.; Balandina, Alsu A.; Solovieva, Svetlana E.; Antipin, Igor S.; Konovalov, Alexander I.
• Is Part Of: Journal of physical organic chemistry. Volume 26:Number 5(2013:May)
• Page Start: 407
• Page End: 414
• Publication Date: 2013-04-04
• Subjects: conformation -- DNMR -- dynamics -- solution state -- quantum chemistry; Chemistry, Physical organic -- Periodicals; 547.1
• DOI: 10.1002/poc.3101
• Languages: English
• ISSNs: 0894-3230

Abstract

Abstract : According to the quantum chemical calculations and Dynamic NMR experiments in the distally disubstituted classical and thiacalix[4]arenes (CCA and TCA) in addition to the C2v symmetrical pinched cone (PC) conformation, the distorted cone (DC) form with an approximate Cs overall symmetry (with two OH groups bonded to one oxygen atom) also corresponds to the energy minimum. Moreover, in DC form, two different mutual orientations of O–R groups at a lower rim lead to two stable conformations: the first ‐ with both these groups directed outward, the second ‐ with both these groups pointing toward the same direction. In CCA, the PC is essentially favoured over the DC, while in TCA, energies of these forms are similar or the latter may be even preferable. Copyright © 2013 John Wiley & Sons, Ltd. Abstract : In distally disubstituted classical and thiacalix[4]arenes (CCA and TCA), the distorted cone (DC ) form with an approximate Cs symmetry corresponds to the energy minimum. In this form, two different mutual orientations of the O–R groups at a lower rim lead to the two stable conformations. In CCA, the pinched cone is essentially favoured versus theDC, while in TCA, energies of these forms are similar or the latter may be even preferable.