Work

Shedding Light on the Capabilities of Heteroditopic Mechanically Interlocked Molecules in Ion-Pair Sensing

Year: 2026

Type: article

Abstract: High Resolution Image Download MS PowerPoint Slide Heterotopic mechanically interlocked molecules contain different binding sites within their structure, allowing them to recognize specific ion pairs (cations and anions) with a high affinity. The employment of heteroditopic receptors offers advantages over monotopic analogues, in general, being composed of both cation and anion binding sites. The present study elucidates the electronic structure-based recognition of anions and cations of a heteroditopic [2]catenane, IO . Spherical cations and anions have been employed. The structure of IO was modified by replacing its original oxygen atoms of the crown-ether moiety by sulfur atoms and σ–hole donor iodines by −Te–CH 3 groups leading to the modified [2]catenanes IS and TeO, respectively. Energy decomposition analysis (EDA) and natural orbital for chemical valence reveals that the cations exhibit the strongest interaction with the binding pockets of all structures, with Cu +, Li +, and Ni 2+ presenting the most stabilizing values, Δ E IO t o t = −198.2, −175.1, and −653.4 kcal·mol –1, and Δ E IS t o t = −226.4, −154.0, −702.5 kcal·mol –1, respectively. In contrast, anion recognition presented to be significantly lower, being purely dependent on the strength of the σ–hole donors and the size of the applied anion, with Cl – exhibiting the most stable interaction, where Δ E IO t o t = −109.9 kcal·mol –1 . It was also found that the anion recognition for this particular molecule does not affect the cation recognition, significantly. The EDA results confirm that changing from a harder (O) to a softer (S) interactive environment will have considerable impact on cation recognition, thereby demonstrating the pivotal role, following the size match rule .

Source: The Journal of Physical Chemistry A

DOI: 10.1021/acs.jpca.5c08037

Authors: Fábio J. Amorim, Felipe R. F. Pagliarini, Renato L. T. Parreira, Giovanni F. Caramori

Institutions: Universidade Federal de Santa Catarina, Universidade de Franca

Language: English

Topic: Supramolecular Chemistry and Complexes

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: hybrid

Funders: Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Universidade Federal de Santa Catarina

Awards: G1842265047, G3016421138, G3330440052, G3690646728