Recognition of nitrate by the ammonium derivative of a 20-membered dioxadiaza-calix[4]arene analog - Solution and solid-state study of the anion binding properties

Ramón Moreno-Corral, Herbert Höpfl*, Anatoly K. Yatsimirsky, Juan Carlos Gálvez-Ruiz, Karen O. Lara

*Autor correspondiente de este trabajo

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

2 Citas (Scopus)

Resumen

A 20-membered dioxadiaza-calix[4]arene analog (1) was combined with a series of inorganic acids to explore the anion-inclusion properties of the corresponding ammonium dication [1-H2]2+. The neutral calix[4]arene analog 1 and six salts of the receptor in the mono- or diprotonated form, [1-H2]Cl2 (2), [1-H2]Br2 (3), [1-H2][MeOSO3]2 (4), [1-H2][NO3]2 (5), [1-H2][ClO4]2 (6), and [1-H][ClO4] (6b), were structurally characterized by single-crystal X-ray diffraction analysis, which enabled a detailed comparative analysis of the non-covalent interactions. The structural comparison showed that the different anions induce conformational changes of the macrocyclic structure, but only NO3- gave a true inclusion complex. Additionally, the tetramethylammonium derivative of 1, [1-Me4]I2 (7), was prepared and structurally characterized. 1H NMR titration studies of [1-H2]2+ in an aqueous-polar solvent mixture (H2O/MeOH, 9:1 v/v, pH 5.5) with a series of organic and inorganic anions gave association constants varying from 1.4 to 84.6 M-1.

Idioma originalInglés
Páginas (desde-hasta)1232-1240
Número de páginas9
PublicaciónTetrahedron
Volumen71
N.º8
DOI
EstadoPublicada - 25 feb. 2015

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© 2015 Elsevier Ltd. All rights reserved.

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