The solid-state structures of organic salts formed by calix[4]arene dihydroxyphosphonic acid with nucleic bases cations: adeninium, cytosinium, guaninium and uracilium

Aleksander Shkurenko, Adina N. Lazar, Dominique Collard, Alda Navaza, Beomjoon Kim, Yannick Tauran, Florent Perret, Catherine Journet-Gautier, Anthony W. Coleman, Kinga Suwinska

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Calix[4]arene dihydroxyphosphonic acid has been demonstrated to possess an interesting range of biological properties, including atypical anti-cancer activity. The robustness of calix[4]arene dihydroxyphosphonic acid and its ubiquitous dimeric motif offers perspectives for pre-defined solid state complexation with small molecules. In the current article we describe co-crystals (organic salts) of calix[4]arene dihydroxyphosphonic acid with four nucleic base cations: adeninium, cytosinium, guaninium and uracilium. A number of characteristic interactions between the components in the four co-crystals are pointed out also using the Hirshfeld surface analysis. All the four co-crystals are based on layers of calix[4]arene dimers, alternating with layers of nucleic acid molecules. Two of the reported crystal structures (cytosinium and guaninium) are 1D channel-type structures, while the two others (adeninium and uracilium) represent 2D channel-type structures. In three out of four reported structures, interactions between the cations of nucleic bases are present generating 1D chains of cations. A constant motif is that the nucleic base is present in a type of cavity formed by one aromatic ring and a phosphonic acid moiety.
Original languageEnglish (US)
Pages (from-to)545-559
Number of pages15
JournalSupramolecular Chemistry
Volume30
Issue number5-6
DOIs
StatePublished - Feb 18 2018

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We thank the Plateforme Lyonnaise d’Analyses Thermiques du LMI (PLAT) for the TG analyses and for help in interpreting the data.

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