Ana Miljkovic

The extraction of technetium, present in nitric acid medium as pertechnetate anion, is an issue in solvent extraction processes used to recover uranium and plutonium. In the present study, a complexing agent is added in the aqueous nitric acid solution to bind selectively the pertechnetate anion and prevent its extraction into the organic phase or to back extract it in the aqueous phase. Several azacryptands with the addition of hydrophilic groups were synthesized to improve the solubility of the previously studied cage molecule in nitric acid medium. Solvent extraction tests reveal that all the synthesized ligands have a similar complexation strength towards pertechnetate and are able to maintain this anion in the aqueous phase (0.5 M HNO₃). These ligands are able to overcome the Hofmeister bias and selectively bind technetium in nitric acid solution. The azacryptand concentration can be increased by a factor of three in the liquid–liquid extraction conditions compared to our previous work. Coordination studies using microcalorimetry, Single Crystal X-Ray Diffraction (SC-XRD), infrared and Raman spectroscopies show the formation of an inclusion complex with hydrogen bonds stabilizing the oxo-anion within the cavity. This solubility improvement is promising for the introduction of this kind of macrocyclic azacryptands in a solvent extraction process.

In this work, we combined smartphone sensing with the indicator displacement approach for the determination of trans,trans-muconic acid (i.e.tt-MA), a benzene biomarker, in urine. Dicopper(II) azacryptate was employed as the receptor. The good match of tt-MA with the receptor cavity was suggested by DFT calculations, and confirmed experimentally by UV-vis titrations in buffered aqueous solutions. The binding constant was determined through fluorimetric titrations using the indicator displacement approach. This method also confirmed the high affinity of the azacryptate for tt-MA in artificial and spiked urine samples. A portable device was then obtained by adsorption of the chemosensing ensemble on silica gel using ELISA-like plastic wells as the support. Indicator displacement was detected and quantified by exposing the microplate to a UV-lamp (366 nm) and recording the RGB values with a smartphone. A good correlation was found between the R index values and urinary tt-MA in the occupational concentration range.

In this work, we employed for the first time a dinuclear bis[tris(2-aminoethyl)amine] cryptate to obtain the self-assembly of pseudorotaxane structures in an aqueous solution. The goal was achieved by exploiting the well-known affinity of the dicopper azacryptate with diphenyl spacers for the terephthalate anion. In particular, a series of molecular threads were synthesized by appending either alkyl or polyoxyethylene chains on both sides of the terephthalate benzene ring. The obtained dicarboxylic acids were precipitated as sodium salts, and their affinity toward the dicopper azacryptate was determined in a methanol/water mixture (pH 7). Experimental investigations showed that the chains’ length and nature have a small impact on the 1:1 binding constants, whose values range between 4.98 and 5.18 log units. Computational studies indicated that the molecular axle is threaded through the azacryptate cavity, with the terephthalate group wedged between the two copper ions, coordinating both of them in the apical position (the one that, in the free azacryptate, is occupied by a water molecule). Compared to the inclusion complex with the plain terephthalate anion, a slight strain was found in the pseudorotaxane structure, induced by the inner chain of the thread inside the cavity. These results may be of great interest in all of the fields of science and technology in which host–guest recognition and molecular cages are applied.

In this work, we have investigated the properties of novel fluorescent semi(thio)carbazone systems with anions by UV-vis, spectrofluorimetric and NMR studies, in acetonitrile and DMSO solutions. Conformational preferences were determined by theoretical calculations within the DFT approach. For the free receptors, these studies pointed out a marked prevalence of anti conformations, which are stabilized by intramolecular H-bonds between the (thio)urea NH group and the imino nitrogen atom. For the julolidine-based thiosemicarbazone system, intermolecular interactions involving the thiourea NH groups and the S atoms of two receptor molecules were also found in the crystals, leading to the formation of supramolecular dimers. Theoretical studies showed that anion binding involved a change of the conformation of the receptors from anti to syn. In the syn isomers, two NH groups actually point in the same direction, thus favouring the binding of anions, e.g. the Y-shaped acetate ion. This thorough study on the novel semi(thio)carbazones provides useful information for the application of this type of molecule in all the fields of chemistry, in which urea-based systems are employed (e.g. anion recognition and transport, catalysis, soft materials, etc.).

In this work, we investigated the dicopper(II) complex of Mozobil^TM as a potential receptor for anions in MeOH and MeOH/water mixture. The results were compared with those obtained for the mononuclear complex, copper(II) benzyl-cyclam as a model system. Experimental investigations were also supported by computational studies on both the dinuclear and the mononuclear species. Among the investigated anionic guests, the dicopper complex showed an outstanding affinity for the pyrophosphate anion, leading to the formation of a stable adduct in MeOH solution. Our computational studies strongly suggested a 2:2 stoichiometry for the adduct. At least in MeOH, this dimeric structure, with two pyrophosphate anions sandwiched between two dicopper Mozobil^TM units, is stabilized by H-bonding interactions between the receptor and pyrophosphate. In MeOH:water mixture, beside the strong competition of solvent, the affinity toward the anion was preserved. We exploited this property to develop a novel indicator displacement assay (IDA) for pyrophosphate in aqueous solution, using Pyrocatechol Violet (PV) as the indicator.

2,3,4,5-Tetrafluorobenzyl and imidazolium groups within an open-chain receptor allow for the effective binding of chloride in organic–water solution.

Novel tripodal 3-iodopyridinium-based receptors were investigated through (i) UV-vis and NMR titrations with anions in solution, (ii) theoretical calculations, and (iii) X-ray diffraction studies. Their anion binding properties were compared to those of the monobranched model and/or non-halogenated model systems. Investigations in acetonitrile pointed out that the iodine atom in the meta position to pyridinium enhances anion affinity. According to computational studies, this effect seemed to depend on the electron-withdrawing nature of the iodine-substituents. Notably, 1 : 1 adducts were observed to form in solution with all the investigated anions. The strong de-shielding effect observed on the receptors' protons upon anion binding indicated their participation in hydrogen-bonds with the coordinated anion. This result was supported by theoretical calculations and, in the solid state, by X-ray diffraction studies on the complexes with nitrate and bromide. In the crystalline state, the pyridinium arms of the tripodal receptor assume a “2-up, 1-down” conformation. Both nitrate and bromide anions are included in the receptor's cavity, forming two hydrogen-bonding interactions with the protons of the “2-up” arms, and one halogen-bonding interaction with the C–I group of a second molecular cation. The combination of hydrogen and halogen bonds leads to supramolecular chains in the crystals.