A new polyazamacrocyclic ligand (called pctga) containing pyridine and N-glutaryl arms has been synthesized as a potential agent for MRI (magnetic resonance imaging). Three series of successive complexes formed with Eu(3+) were characterized by at least two of the following methods: potentiometry, EXAFS or luminescence spectrometry. In the immediate complexes [EuH(h)(pctga)(H2O)6](h-3)+**, the metal ion is bound to the oxygen atoms of the three internal carboxylate groups and to six water molecules. As the lanthanide moves into the macrocyclic cavity, these species rapidly evolve into the intermediate metastable complexes [EuH(h)(pctga)(H2O)4](h-3)+*. The formation of two new bonds with the nitrogen atoms of the tetraazamacrocycle decreased the number of coordinated water molecules to four. In the final thermodynamically stable complexes [EuH(h)(pctga)(H2O)(2)](h-3)+, the pctga is bound to the europium(III) in a heptadentate manner, via the four nitrogen atoms of the tetraazamacrocycle and the three oxygen atoms of the internal carboxylate groups. The coordination number of the metal ion is completed to nine with two inner-sphere water molecules. The mean hydration numbers were calculated from the values of the bimolecular quenching constant k(q) of the luminescence species. The thermodynamic parameters corresponding to the protonation constants of the ligand and to the formation constants of the various intermediate and final complexes were determined from potentiometric measurements. They show that the complex species have some specific thermodynamic and structural properties inherent to the N-glutaryl groups and to the pyridine cycle. The insertion of this aromatic substructure rigidifies the ligand and sensibly diminishes the value of the overall formation constant (log beta(110) = 18.66(5)). This whole study allows us to propose a complexation mechanism for the system Eu(3+)/pctga in solution which is a mixture of the ones determined for the ligands dota and tced.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/b700673j | DOI Listing |
J Chem Inf Model
January 2025
Donostia International Physics Center (DIPC), 20018 Donostia-San Sebastián, Spain.
Desalination of seawater by forward osmosis is a technology potentially able to address the global water scarcity problem. The major challenge limiting its widespread practical application is the design of a draw solute that can be separated from water by an energetically efficient process and then reused for the next cycle. Recent experiments demonstrate that a promising draw solute for forward-osmosis desalination is tetrabutylphosphonium 2,4,6-trimethylbenzenesulfonate ([P][TMBS]).
View Article and Find Full Text PDFAcc Chem Res
January 2025
Center for Molecular Spectroscopy and Dynamics, Institute for Basic Science, Seoul 02841, Korea.
ConspectusWater-in-salt electrolytes (WiSEs) are promising electrolytes for next-generation lithium-ion batteries (LIBs), offering critical advantages like nonflammability and improved safety. These electrolytes have extremely high salt concentrations and exhibit unique solvation structures and transport mechanisms dominated by the formation of ion networks and aggregates. These ion networks are central to the performance of WiSEs, govern the transport properties and stability of the electrolyte, deviating from conventional dilute aqueous or organic electrolytes.
View Article and Find Full Text PDFNutrients
December 2024
Department of Pharmacology and Nutritional Sciences, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
High sugar intake, particularly fructose, is implicated in obesity and metabolic complications. On the other hand, fructose from fruits and vegetables has undisputed benefits for metabolic health. This raises a paradoxical question-how the same fructose molecule can be associated with detrimental health effects in some studies and beneficial in others.
View Article and Find Full Text PDFInt J Mol Sci
January 2025
Faculty of Chemistry and Pharmacy, University of Opole, Oleska 48, 45-052 Opole, Poland.
O-Methyldehydroserine, ΔSer(Me), is a non-standard α,β-dehydroamino acid, which occurs naturally in Cyrmenins with potential pharmaceutical application. The C-terminal part and the side chain of the ΔSer(Me) residue constitute the β-methoxyacrylate unit, responsible for antifungal activity of Cyrmenins. The short model, Ac-ΔSer(Me)-OMe, was analyzed considering the geometrical isomer Z () and E ().
View Article and Find Full Text PDFInt J Mol Sci
December 2024
Institute of Biomedical Chemistry, Pogodinskaya Str., 10, Moscow 119121, Russia.
Biomacromolecules generally exist and function in aqueous media. Is it possible to estimate the state and properties of molecules in an initial three-dimensional colloidal solution based on the structure properties of biomolecules adsorbed on the two-dimensional surface? Using atomic force microscopy to study nanosized objects requires their immobilization on a surface. Particles undergoing Brownian motion in a solution significantly reduce their velocity near the surface and become completely immobilized upon drying.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!