Intramolecular deactivation processes in complexes of salicylic acid or glycolic acid with Eu(III).

The complexation of Eu(III) by 2-hydroxy benzoic acid (2HB) or glycolic acid (GL) was investigated using steady-state and time-resolved laser spectroscopy. Experiments were carried out in H(2)O as well as in D(2)O in the temperature range of 80KF7(0) transition, (iii) the width of the D5(0)-->F7(0) transition, and (iv) the asymmetry ratio calculated from the luminescence intensities of the D5(0)-->F7(2) and D5(0)-->F7(1) transition, respectively. The differences in ligand-related luminescence quenching are discussed. Based on the temperature dependence of the luminescence decay times an activation energy for the ligand-specific non-radiative deactivation in Eu(III)-2HB or Eu(III)-GL complexes was determined. It is stressed that ligand-specific quenching processes (other than OH quenching induced by water molecules) need to be determined and considered in detail, in order to extract speciation-relevant information from luminescence data (e.g., estimation of the number of water molecules n(H(2)0) in the first coordination sphere of Eu(III)). In case of 2HB, conclusions drawn from the evaluation of the Eu(III) luminescence are compared with results of a X-ray structure analysis.

Europium3+: an efficient luminescence probe for the Si to Al ratio and silylation effects in the microporous-mesoporous Zeogrid materials.

The optical response of europium ions in the parent (non-silylated) and silylated microporous-mesoporous Zeogrid materials was investigated in detail in relation to Zeogrid structure. All materials were characterized using nitrogen adsorption isotherms, powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetry, and time-resolved photoluminescence spectroscopy. A two europium species distribution with distinct luminescence spectra and lifetimes was found for both parent and silylated Zeogrid. In the parent Zeogrid, the short-lived europium species is characterized by the intensity ratio R=I(5D0-(7)F2)/I(5D0-(7)F1) or asymmetry values of approximately 0.4-0.7 and photoluminescence (PL) lifetimes of 110-125 micros and therefore is assigned to an almost fully hydrated europium species. In the silylated Zeogrid, the short-lived europium species is characterized by asymmetry values of 1.0-2.4 and lifetimes of 160-180 micros suggesting a relatively distorted europium environment. The long-lived europium species exhibits similar asymmetry ratios in the parent and silylated Zeogrid, which vary between 5.0 and 6.2 with increasing Si to Al ratio from 25 to 150 and slightly different PL lifetimes. The mechanism responsible for the intensity of the electric and magnetic forbidden 5D0-(7)F0 transition was determined to be J-mixing of the 7F2 into the 7F0 state through the axial second-order crystal-field potential. The comparison between the photoluminescence properties of europium in the parent and silylated Zeogrid demonstrates that the effects of rehydration were strongly suppressed following silylation.

Alkaline hydrolysis of humic substances--spectroscopic and chromatographic investigations.

To find out more on the structure of humic substances (HS), isolated dissolved organic carbon (DOC) samples from a brown water lake and a wastewater effluent were fractionated and subjected to alkaline hydrolysis. UV/Vis and fluorescence spectroscopy, as well as size-exclusion chromatography with on-line detection of UV absorption, fluorescence and DOC concentration were used to investigate the structural changes caused by the hydrolysis reaction. Following hydrolysis, the fluorescence intensity increased considerably despite a decrease in the UV absorption. The UV absorption and the DOC data from the SEC experiments revealed a strong shift to smaller molecular sizes after hydrolysis. The spectra of the hydrolysed samples, as well as the size-exclusion chromatograms, were compared to spectra of hydroxybenzoic acids and hydroxycinnamic acids. From this comparison, it can be concluded that the hydrolysis products have a structure similar to these organic acids.

Sorption of phenols to dissolved organic matter investigated by solid phase microextraction.

The sorption of phenol and different halogenated phenols to natural organic matter of a brown water lake (HO14), of a compost extract, of Aldrich humic acid (Aldrich-HA), and to the protein bovine serum albumin (BSA) was investigated using solid phase microextraction (SPME). The limit of determination for the SPME analysis was < 15 microg/l for all phenols investigated. The extraction coefficients K(F) were calculated according to a first-order extraction kinetics. In general, the extraction equilibrium was established faster due to the presence of dissolved organic matter (DOM). The highest sorption capacity of phenols was observed for BSA with log K(OC) values in the range between 2 and 6. For the compost extract and HO14 only a small sorption of the investigated phenols was determined. On the other hand, Aldrich humic acid showed a reasonable sorption of phenols with log K(OC) values between 2 and 3. The sorption to DOM decreased when the pH of the solution was increased.

Temperature and quenching studies of fluorescence polarization detection of DNA hybridization.

The effects of temperature and collisional quenching on fluorescence polarization detection of DNA hybridization were studied using measurements of fluorescence intensity and anisotropy and the dynamic decay of these properties. Three different tethers, 3, 6, and 12 carbons in length, were used to attach fluorescein label to the 5' end of the 33-base oligomers. Perrin plots showed that the effective rotating volume decreases with increasing tether length and approximately doubles upon hybridization. Hybridization increases the association between the tethered dye and the DNA for the shorter tethers but displaces the fluorescein on the 12C tether from the DNA, forcing it into greater contact with the bulk solution. The 6C tether appears to promote sequence-specific interaction between fluorescein label and the oligomer, which causes unexpectedly high anisotropy at higher temperatures and increased protection from collisional quenching. In all cases, there appear to exist several possible conformations for the tethered fluorescein. As temperature is increased, these conformations tend to collapse into a single, average or preferred, conformation. The results demonstrate the importance of the selection of tether, dye, and DNA probe in designing a polarization strategy for detection of DNA hybridization, particularly with respect to tether length and DNA probe sequence.

Hybridization of fluorescein-labeled DNA oligomers detected by fluorescence anisotropy with protein binding enhancement.

Fundamental aspects of the application of fluorescence anisotropy to detect the hybridization of fluorescein-labeled DNA oligomers were explored. The oligomers included a binding site for the EcoRI restriction enzyme, which binds to double-stranded DNA and is used in this work to enhance the difference between the anisotropies of the single-stranded and double-stranded oligomers by increasing the effective volume of the latter. The fluorescence anisotropy increases upon hybridization and further upon binding of EcoRI to the double strand. By varying the length of the tether used to attach the fluorescein to the 5' end of the oligonucleotide, it was found that a 6-carbon tether was optimal, providing the most dramatic increases in anisotropy in the presence of EcoRI. Dynamic fluorescence anisotropy (DFA) provided insight into the increases in steady-state anisotropy. In most cases, the best fits to the DFA data were obtained using a biexponential decay model, which describes an anisotropic rotator. Upon hybridization, the faster rotational motion is more hindered, and the contribution of the slower rotational component is increased. This effect is enhanced by binding of EcoRI to the double strand, especially when the EcoRI binding site is near the fluorescein at the 5' end and the tether length is in the optimal range. Because the rotational correlation time of the slower anisotropy decay component is much longer than the fluorescence lifetime, it is possible in some cases to reduce the anisotropic rotator model to the special limiting case of a hindered rotator.

Fluorescence spectroscopy of polynuclear aromatic compounds in environmental monitoring.

The occurrence of polynuclear aromatic compounds (PAC) in the environment and experimental techniques suitable for the detection of PAC in environmental compartments are briefly reviewed. The specific requirements for on-site andin situ environmental analysis are outlined. Particular emphasis is given to fluorescence spectroscopic techniques for the investigation of humic acid- and soil-containing samples. Some examples of studies in the literature on Shpol'skii and jet spectroscopy and on laser-induced fluorescence (OF) measurements of PAC and mineral oils are highlighted. Contaminants in the environment are usually encountered as multicomponent mixtures in very complex matrices. Total fluorescence analysis in combination with the chemometrical technique of rank annihilation factor analysis (RAFA) was employed for the evaluation of a six-component PAC mixture in toluene. It was shown that even in the presence of strong spectral overlap the qualitative identification of all compounds and the reliable quantification of five substances was possible. Results are presented from our stationary and time-resolved fluorescence investigations of the interactions between pyrene and humic acid in water. The Stern-Volmer analysis showed a significant effect of pH on the static quenching efficiency which can be explained by the pH-dependent macromolecular structure of humic acids. Preliminary results from studies of the deactivation of triplet PAC and quenching of delayed fluorescence by humic acid are reported. LIF measurements of mineral oils directly from soil surfaces and of a model oil in a soil column were performed with a fiber-optic coupled multichannel spectrometer. The fluorescence intensity/ concentration relationships were established for a crude and a fuel oil; the corresponding lower limits of detection (LOD) were determined to be 0.025 and 0.125% m/m (mass/mass percentages). These detection limits are compared with realistic oil contaminations of soils. In a soil column designed to mimic fixed-bed bioreactors the distributions of fluorescence signal intensities from a perylene-doped model oil before and after water flooding were determined. These results fromin situ measurements can provide a quantitative basis for the modelling of temporal and spatial contaminants' distributions in reactor design.