Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/14062
Title: A theoretical mechanistic study of [K ⊂ [2.2.2]]<sup>+</sup> enantiomerization
Authors: Balović J.
Ćoćić, Dušan
Đorđević, Slađana
Radenkovic, Slavko
van Eldik R.
Puchta, Ralph
Journal: Journal of Physical Organic Chemistry
Issue Date: 1-Jan-2021
Abstract: Density functional calculations at three different levels of theory (B3LYP/LANL2DZp, B3LYP-GD3/LANL2DZp, and ωB97XD/def2tzvp) were applied to different conformers of the Lehn-type macrobicyclic polyether cryptate complex [K ⊂ [2.2.2]]+ to construct the enantiomerization pathway and to compute the energy barrier for the change in symmetry. Changes in the conformation of the investigated complex are discussed in terms of energy and geometric criteria, where changes in the structures follow a trend of activation energies prohibiting the achiral pathways. The investigated D3-symmetric cryptate [K ⊂ [2.2.2]]+ shows enantiomerization through an all chiral five step pathway with two local minima (C2 and C2′) and three C1 transition states ending in the D3′-symmetric cryptate [K ⊂ [2.2.2]]+, the mirror image of the starting structure. The potential achiral transition states are higher order saddle points with a minimum twice as high in energy as an all-chiral path. This study unambiguously accounts for Lehn's NMR data showing fluxionality of the studied complex. The obtained results were further rationalized by means of energy decomposition analysis (EDA) and natural bond orbital (NBO) calculations performed for the metal cation and the host in its different conformations.
URI: https://scidar.kg.ac.rs/handle/123456789/14062
Type: article
DOI: 10.1002/poc.4289
ISSN: 08943230
SCOPUS: 85115841747
Appears in Collections:Faculty of Science, Kragujevac

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