Selective and pH-Independent Detection of Ba in Water by a Benzo-21-crown-7-Functionalized BODIPY.

Herein, we report on highly Ba selective fluorescence sensing in water by a fluorescent probe consisting of a benzo-21-crown-7 as a Ba binding unit (ionophore) and a tetramethylated BODIPY fluorophore as a fluorescence reporter. This fluorescent probe showed a Ba induced fluorescence enhancement (FE) by a factor of 12±1 independently of the pH value and a high Ba sensitivity with a limit of detection (LOD) of (17.2±0.

Interdisciplinary Round-Robin Test on Molecular Spectroscopy of the U(VI) Acetate System.

A comprehensive molecular analysis of a simple aqueous complexing system-U(VI) acetate-selected to be independently investigated by various spectroscopic (vibrational, luminescence, X-ray absorption, and nuclear magnetic resonance spectroscopy) and quantum chemical methods was achieved by an international round-robin test (RRT). Twenty laboratories from six different countries with a focus on actinide or geochemical research participated and contributed to this scientific endeavor. The outcomes of this RRT were considered on two levels of complexity: first, within each technical discipline, conformities as well as discrepancies of the results and their sources were evaluated.

Intramolecular deactivation processes of electronically excited Lanthanide(III) complexes with organic acids of low molecular weight.

The luminescence of Lanthanide(III) complexes with different model ligands was studied under direct as well as sensitized excitation conditions. The research was performed in the context of studies dealing with deep-underground storages for high-level nuclear waste. Here, Lanthanide(III) ions served as natural analogues for Actinide(III) ions and the low-molecular weight organic ligands are present in clay minerals and furthermore, they were employed as proxies for building blocks of humic substances, which are important complexing molecules in the natural environment, e.

A Highly K(+)-Selective Two-Photon Fluorescent Probe.

A highly K(+)-selective two-photon fluorescent probe for the in vitro monitoring of physiological K(+) levels in the range of 1-100 mM is reported. The two-photon excited fluorescence (TPEF) probe shows a fluorescence enhancement (FE) by a factor of about three in the presence of 160 mM K(+), independently of one-photon (OP, 430 nm) or two-photon (TP, 860 nm) excitation and comparable K(+)-induced FEs in the presence of competitive Na(+) ions. The estimated dissociation constant (Kd ) values in Na(+)-free solutions (Kd (OP) =(28±5) mM and Kd (TP)=(36±6) mM) and in combined K(+)/Na(+) solutions (Kd (OP) =(38±8) mM and Kd (TP)=(46±25) mM) reflecting the high K(+)/Na(+) selectivity of the fluorescent probe.

Fluorescence lifetime-based sensing of sodium by an optode.

We report a 1,2,3-triazol fluoroionophore for detecting Na(+) that shows in vitro enhancement in the Na(+)-induced fluorescence intensity and decay time. The Na(+)-selective molecule 1 was incorporated into a hydrogel as a part of a fiber optical sensor. This sensor allows the direct determination of Na(+) in the range of 1-10 mM by measuring reversible fluorescence decay time changes.

Formation of a Eu(III) borate solid species from a weak Eu(III) borate complex in aqueous solution.

In the presence of polyborates (detected by (11)B-NMR) the formation of a weak Eu(III) borate complex (lg β11 ~ 2, estimated) was observed by time-resolved laser-induced fluorescence spectroscopy (TRLFS). This complex is a precursor for the formation of a solid Eu(III) borate species. The formation of this solid in solution was investigated by TRLFS as a function of the total boron concentration: the lower the total boron concentration, the slower is the solid formation.

Combining spectroscopic and potentiometric approaches to characterize competitive binding to humic substances.

In an area that contains high concentrations of natural organic matter, it is expected that it plays an important role on the behavior of rare earth elements (REE), like europium, and of trivalent actinides. Competitive interactions with H+, inorganic species, major cations, e.g.

Fluorescence quenching and luminescence sensitization in complexes of Tb3+ and Eu3+ with humic substances.

Intrinsic fluorescence quenching of humic substances (HS) and the sensitization of Ln3+ luminescence (Ln3+ = Tb3+, Eu3+) in HS complexes were investigated. Both measurements yielded complementary information on the complexation of metals by HS. Large differences between fulvic acids (FA) and humic acids (HA) were found.