TY - JOUR
T1 - 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
AU - Moreno-Corral, Ramón
AU - Höpfl, Herbert
AU - Yatsimirsky, Anatoly K.
AU - Gálvez-Ruiz, Juan Carlos
AU - Lara, Karen O.
N1 - Publisher Copyright:
© 2015 Elsevier Ltd. All rights reserved.
PY - 2015/2/25
Y1 - 2015/2/25
N2 - 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.
AB - 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.
KW - Anion recognition
KW - Calixarene analog
KW - Cyclophane
KW - Host-guest chemistry
KW - Nitrate receptor
KW - X-ray structure analysis
UR - http://www.scopus.com/inward/record.url?scp=84922214734&partnerID=8YFLogxK
U2 - 10.1016/j.tet.2015.01.005
DO - 10.1016/j.tet.2015.01.005
M3 - Artículo
SN - 0040-4020
VL - 71
SP - 1232
EP - 1240
JO - Tetrahedron
JF - Tetrahedron
IS - 8
ER -