Supramolecular interactions in the heteroarylimine-substituted calix[4]arenes: the formation of cyclic dodecanuclear palladium aggregates

• Published in: Supramolecular chemistry Vol. 33; no. 4; pp. 129 - 142
• Main Authors: Tsymbal, Lyudmila V., Rodik, Roman V., Danylyuk, Oksana, Suwinska, Kinga, Lipkowski, Janusz, Kalchenko, Vitaly I., Lampeka, Yaroslaw D.
• Format: Journal Article
• Language: English
• Published: Taylor & Francis 03.04.2021
• Subjects: Calixarenes; calixdiquinones; crystallography; Pd(ii) complexes; supramolecular organisation
• ISSN: 1061-0278; 1029-0478
• DOI: 10.1080/10610278.2021.1944632

Two new derivatives of calix[4]arene bearing on the upper rim 2-thiopenyl (Thicalix) or 2-pyridyl (Pycalix) Schiff-base substituents have been synthesised and characterised by IR, NMR, MS, and single crystal X-ray diffraction techniques. It was shown that the interaction of Thicalix with the copper(II) and palladium(II) ions is accompanied by hydrolysis of the azomethine bonds with subsequent oxidation of the aminophenolic fragment to diquinone Diquin, while the reaction of potassium tetrachloropalladate(II) with Pycalix results in the formation of metallocompex with 1:2 calix[4]arene/Pd(II) ratio. The single crystal X-ray diffraction analysis of Thicalix (1), the complex [(PdCl 2 ) 2 (Pycalix)] (2) and Diquin (3) revealed that all compounds form molecular crystals as a result of numerous supramolecular interactions involving C − H···O, C − H···Cl, and C − H···π contacts. For 1 and 3 such interactions result in formation of dimers, while in 2 the dodecanuclear palladium aggregates composed of six calix[4]arene moieties are formed.