New uranium(vi) and isothiouronium complexes: synthesis, crystal structure, spectroscopic characterization and a DFT study. Issue 34 (19th August 2020)

• Record Type: Journal Article
• Authors: Grabias, Ewelina; Tarasiuk, Bogdan; Dołęga, Anna; Majdan, Marek
• Is Part Of: CrystEngComm. Volume 22:Issue 34(2020)
• Page Start: 5678
• Page End: 5689
• Publication Date: 2020-08-19
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/d0ce00746c
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : U(vi ) and isothiouronium salts create a strong charge-assisted network of hydrogen bonds and ionic interactions. Abstract : The crystal structures of S, S′ -2, 5-dimethylbenzene-1, 4-diylbis(methylisothiouronium) diacetate (1 _ac ), S, S′ -2, 5-dimethylbenzene-1, 4-diylbis(methylisothiouronium) dichloride (1 _Cl ), 1 _U complex, S, S′ -naphthalene-1, 4-diylbis(methylisothiouronium) dichloride (2 _Cl ), and 2 _U complex were determined for the first time. The supramolecular structures of the compounds obtained are mainly based on hydrogen bonding and ionic interactions between the isothiouronium cations and the counter anions Cl −, CH3 COO −, and [UO2 (CH3 COO)3 ] − . Their structural and spectroscopic properties were studied, and the results of DFT calculations were compared with the experimental findings to provide insights into the properties of these new compounds. The DFT calculations indicate a strong preference for the formation of the outer-sphere complex (ion-pair) between the uranyl species and an isothiouronium cation, and very large stabilization energies of the interactions, which can be utilized for the selective binding of U(vi ). The compounds obtained are the first f-element and isothiouronium salt complexes described so far.