Optical Activity in Saturated Cyclic Amines: Untangling the Roles of Nitrogen-Inversion and Ring-Puckering Dynamics.

Abstract

The dispersive optical activity of two saturated cyclic amines, (R)-2-methylpyrrolidine (R-2MPY) and (S)-2-methylpiperidine (S-2MPI), has been interrogated under isolated and solvated conditions to elucidate the roles of large-amplitude motion associated with nitrogen-center inversion and ring-puckering dynamics. Experimental optical rotatory dispersion profiles were almost mirror images of one another and displayed parallel solvent dependencies. Quantum-chemical analyses built on density-functional and coupled-cluster methods revealed four low-lying conformers for each molecule, which are distinguished by axial/equatorial orientations of their amino hydrogens and methyl substituents. Chiroptical signatures predicted for these species were combined through an independent-conformer ansatz to simulate the ensemble-averaged response, with a polarizable continuum model (PCM) being used to treat implicit solute-solvent interactions. The intrinsic behavior observed for isolated (gaseous) R-2MPY and S-2MPI was reproduced best by merging coupled-cluster (CCSD) estimates of rotatory powers with thermal population fractions deduced from complete basis set (CBS-APNO) free-energy calculations. Although prior claims of sizable chiroptical contributions arising from helically twisted (chiral) heterocyclic frameworks could be discounted, less satisfactory agreement between experiment and theory was realized for solution phases. Response properties sustained modest isomer-dependent changes in the presence of PCM solvation, but the corresponding energy metrics showed systematic trends, whereby structures having larger electric-dipole moments were stabilized preferentially in media of high polarity. Despite the fact that R-2MPY conformations were predicted to undergo a progressive reordering of their relative energies across the six solvents of interest, S-2MPI was found to exhibit more pronounced solvent-induced perturbations at long wavelengths (viz., in regions far removed from electronic resonances). Experimental results are discussed in terms of the distinct ring-puckering mechanisms for R-2MPY and S-2MPI, which are expected to be dominated by hindered pseudorotation among envelope/twist motifs and semi-inversion between chairlike antipodes, respectively.