Crystal structures of 2,2′:6′,2″-terpyridine uranyl chlorides molecular assemblies and their luminescence signatures

A series of three compounds bearing uranyl cations and 2,2′:6′,2″-terpyridine (terpy) has been hydrothermally synthesized from uranium tetrachloride aqueous solution. An oxidation process into the hexavalent state has been observed for uranium in these synthesis conditions, together with the crystallization of different phases, which have been characterized by single-crystal X-ray diffraction analysis. The tetrachloridodioxidouranate terpyridinium salts UO2Cl4·H2terpy·H2O (1) and UO2Cl4·(H2terpy)2·2Cl (2) consist of the molecular assemblies of tetrachloro-uranyl anions ([UO2Cl4]2−, square plane bipyramidal environment), isolated to each other via the doubly protonated H2terpy molecules. The latter chelate either water (1) or chlorine anions (2). The addition of organic base such as pyridine favored the crystallization of the complex, UO2Cl2(terpy) (3), with the neutral terpy moiety coordinating one uranyl center via the nitrogen atoms of the pyridyl rings. It resulted in one uranyl center bonded to three nitrogen and two terminal chlorine anions, located in a distorted equatorial plane and two terminal perpendicular uranyl oxygens in apical position of a pentagonal bipyramid ([UO2Cl2N3]). Different π–π interactions between the pyridyl rings of neighboring terpy molecules also occur for these complexes. Fluorescence spectroscopy of these different complexes has been measured at room temperature and 77 K showing the various local environments of the emitting centers.

Three uranyl chloro compounds with diprotonated or chelating terpyridine molecules have been isolated; their photoluminescence properties have been evaluated at room temperature and 77 K.Figure optionsDownload as PowerPoint slide