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Stereochemical Inversion of Rim-Differentiated Pillar[5]arene Molecular Swings

Ke Du, Paul Demay‐Drouhard, Kushal Samanta, Shunshun Li, Tushar Ulhas Thikekar, Haiying Wang, Minjie Guo, Barend van Lagen, Han Zuilhof, Andrew C.‐H. Sue

2020The Journal of Organic Chemistry41 citationsDOIOpen Access PDF

Abstract

To investigate the dynamic stereochemical inversion behavior of pillar[5]arenes (P[5]s) in more detail, we synthesized a series of novel rim-differentiated P[5]s with various substituents and examined their rapid rotations by variable-temperature NMR (203–298 K). These studies revealed for the first time the barrier of “methyl-through-the-annulus” rotation (ΔG‡ = 47.4 kJ·mol–1 in acetone) and indicated that for rim-differentiated P[5]s with two types of alkyl substituents, the smaller rim typically determines the rate of rotation. However, substituents with terminal C═C or C≡C bonds give rise to lower inversion barriers, presumably as a result of attractive π–π interactions in the transition state. Finally, data on a rim-differentiated penta-methyl-penta-propargyl P[5] exhibited the complexity of the overall inversion dynamics.

Topics & Concepts

ChemistryPillarInversion (geology)StereochemistryComputational chemistryPaleontologyStructural engineeringGeologyStructural basinEngineeringSupramolecular Chemistry and ComplexesAdvanced NMR Techniques and ApplicationsMolecular spectroscopy and chirality
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