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1.
The thermodynamic model of inorganic arsenic was validated by comparing the predicted As(III) concentration with the experimentally determined one in several river waters samples of the Basque Country (Spain) collected in two sampling campaigns: spring and autumn 2000. This model takes into account the acid-base equilibria of As(III) and As(V) together with the redox equilibria between the H3AsO3 and H3AsO4 species. A correct prediction of As(III) concentration requires the knowledge of the total concentration of arsenic, pH, redox potential (referred to hydrogen electrode), and ionic strength values of the solution. The estimation of the activity coefficients of the arsenic species was performed by means of the Modified Bromley’s Methodology (MBM).In order to perform the experimental As(III) determination, an analytical method was implemented by using an ion exchange separation of As(III)/As(V) on a continuous FIA-IE-HG-AAS system. The total arsenic concentration was determined together with total concentration of the main alkaline or alkaline-earth metals and anions in the natural waters. Temperature compensated measurements of the pH and redox potentials were made in-situ at the sampling sites.For both seasonal campaigns, the agreement between predicted and experimental As(III) is really high for those samples belonging to non polluted river waters. 相似文献
2.
Dr. Olatz Larrañaga Prof. Dr. Ana Arrieta Prof. Dr. Célia Fonseca Guerra Prof. Dr. F. Matthias Bickelhaupt Dr. Abel de Cózar 《化学:亚洲杂志》2021,16(4):315-321
We have quantum chemically studied the structure and nature of alkali- and coinage-metal bonds (M-bonds) versus that of hydrogen bonds between A−M and B− in archetypal [A−M⋅⋅⋅B]− model systems (A, B=F, Cl and M=H, Li, Na, Cu, Ag, Au), using relativistic density functional theory at ZORA-BP86-D3/TZ2P. We find that coinage-metal bonds are stronger than alkali-metal bonds which are stronger than the corresponding hydrogen bonds. Our main purpose is to understand how and why the structure, stability and nature of such bonds are affected if the monovalent central atom H of hydrogen bonds is replaced by an isoelectronic alkali- or coinage-metal atom. To this end, we have analyzed the bonds between A−M and B− using the activation strain model, quantitative Kohn-Sham molecular orbital (MO) theory, energy decomposition analysis (EDA), and Voronoi deformation density (VDD) analysis of the charge distribution. 相似文献
3.
Manon Catherin Olatz Uranga-Barandiaran Arnaud Brosseau Dr. Rémi Métivier Dr. Gabriel Canard Dr. Anthony D'Aléo Dr. David Casanova Prof. Frédéric Castet Dr. Elena Zaborova Prof. Frédéric Fages 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(17):3818-3828
We describe the synthesis of a series of covalently linked dimers of quadrupolar curcuminoid-BF2 dyes and the detailed investigation of their solvent-dependent spectroscopic and photophysical properties. In solvents of low polarity, intramolecular folding induces the formation of aggregated chromophores, the UV/Vis absorption spectra of which display the optical signature characteristic of weakly-coupled H-aggregates. The extent of folding and, in turn, of ground-state aggregation is strongly dependent on the nature of the flexible linker. Steady-state and time-resolved fluorescence emission spectroscopies show that the Frenkel exciton relaxes into a fluorescent symmetrical excimer state with a long lifetime. Furthermore, our in-depth studies show that a weakly emitting excimer lies on the pathway toward a photocyclomer. Two-dimensional 1H NMR spectroscopy and density functional theory (DFT) allowed the structure of the photoproduct to be established. To our knowledge, this represents the first example of a [2π+2π] photodimerization of the curcuminoid chromophore. 相似文献
4.
New Insights into the Reactivity of Cisplatin with Free and Restrained Nucleophiles: Microsolvation Effects and Base Selectivity in Cisplatin–DNA Interactions 下载免费PDF全文
Dr. Abel de Cózar Dr. Olatz Larrañaga Prof. Dr. F. Matthias Bickelhaupt Dr. Eider San Sebastián Elisabeth Ortega‐Carrasco Dr. Jean‐Didier Maréchal Prof. Agustí Lledós Prof. Dr. Fernando P. Cossío 《Chemphyschem》2016,17(23):3932-3947
The reactivity of cisplatin towards different nucleophiles has been studied by using density functional theory (DFT). Water was considered first to analyze the factors that govern the transformation of cisplatin into more electrophilic aquated species by using an activation‐strain model. It was found that the selectivity and reactivity of cisplatin is a delicate trade‐off between strain and interaction energies and that the second chloride is a worse leaving group than the first. When similar studies were carried out with imidazole, guanine (G), and adenine (A), it was found that in general the second nucleophilic substitution reactions have lower activation barriers than the first ones. Finally, simulations of the structural restrictions imposed by the DNA scaffold in intra‐ and interstrand processes showed that the geometries of the reaction products are nonoptimal with respect to the unrestrained A and G nucleophiles, although the energetic cost is not considerable under physiological conditions, which thus permits nucleophilic substitution reactions that lead to highly distorted DNA. 相似文献
5.
Protonation constants of arsenic acid were determined at different ionic strengths in NaClO(4) (0.1, 0.5, 1.0, 3.0 mol dm(-3)), NaCl (0.5 and 1.0 mol dm(-3)) and KCl (0.5, 1.0 and 3.0 mol dm(-3)) ionic media by means of a potentiometric study. The distribution of arsenate species was defined depending on two important variables in natural environments: pH and composition. All the experimentation was performed at 25 degrees C. The differences found in the protonation constants for different medium compositions, were explained by the different behaviour of the interaction parameters of the species considered in the different media and ionic strengths. These parameters were reported for all hydrolitic As(V) species and were calculated using the Modified Bromley's Methodology (MBM). The corresponding thermodynamic stepwise formation constants were also determined (log degrees K(1)=11.58+/-0.01, log degrees K(2)=7.06+/-0.01, log degrees K(3)=2.25+/-0.01). All the results obtained showed not only the importance of the ionic strength but also of the composition of the ionic medium on the distribution of the acid-base species of As(V) as a function of pH in natural waters. 相似文献
6.
Iparraguirre A Navarro P Prieto A Rodil R Olivares M Fernández LÁ Zuloaga O 《Analytical and bioanalytical chemistry》2012,402(9):2897-2907
Membrane-assisted solvent extraction coupled to large volume injection in a programmable temperature vaporisation injector
using gas chromatography–mass spectrometry analysis was optimised for the simultaneous determination of a variety of endocrine
disrupting compounds in environmental water samples (estuarine, river and wastewater). Among the analytes studied, certain
hormones, alkylphenols and bisphenol A were included. The nature of membranes, extraction solvent, extraction temperature,
solvent volume, extraction time, ionic strength and methanol addition were evaluated during the optimisation of the extraction.
Matrix effects during the extraction step were studied in different environmental water samples: estuarine water, river water
and wastewater (influent and effluent). Strong matrix effects were observed for most of the compounds in influent and effluent
samples. Different approaches were studied in order to correct or minimise matrix effects, which included the use of deuterated
analogues, matrix-matched calibration, standard addition calibration, dilution of the sample and clean-up of the extract using
solid-phase extraction (SPE). The use of deuterated analogues corrected satisfactorily matrix effect for estuarine and effluent
samples for most of the compounds. However, in the case of influent samples, standard addition calibration and dilution of
the sample were the best approaches. The SPE clean-up provided similar recoveries to those obtained after correction with
the corresponding deuterated analogue but better chromatographic signal was obtained in the case of effluent samples. Method
detection limits in the 5–54 ng L−1 range and precision, calculated as relative standard deviation, in the 2–25% range were obtained. 相似文献
7.
Larreta J Vallejo A Bilbao U Usobiaga A Arana G Zuloaga O 《Journal of separation science》2007,30(14):2293-2304
Odorous organic compounds from liquid and gas samples of animal wastes were studied by headspace (HS)-solid-phase microextraction (SPME)-GC-MS. 1-Pirenyldiazomethane (PDAM) was adsorbed/absorbed on the SPME fibre in order to obtain the corresponding ester derivatives during the preconcentration step. The SPME fibre was immersed into a PDAM solution. Then, the SPME fibre was withdrawn and exposed to the HS of the liquid cow slurry. This way derivatisation of VFAs took place in the SPME fibre together with the preconcentration of the rest of the analytes of interest. The analytes were desorbed in the hot injection port (300 degrees C) of a GC-MS for 3 min. Four different fibre types and different immersion periods of the fibre in the PDAM solution were studied in order to obtain the best sensitivity with the selected fibre. Accuracy, precision and the LODs were calculated using spiked liquid and gas samples. The possibility of storing liquid samples after sampling by preconcentration on the fibre was also considered. Storage time and temperature were studied. The optimised method was applied to the determination of the analytes in liquid and gas samples from cow slurries from an intensive production farm. 相似文献
8.
Production of artifact methylmercury (MeHg+) during the analysis of two certified reference sediments, CRM-580 and IAEA-405, was investigated. Leaching of the analyte from the solid sample was achieved by ultrasound assisted acidic extraction. The aqueous leachate was either ethylated (NaBEt4) or phenylated (NaBPh4) using acetic/acetate or citric/citrate to buffer the solution. Preconcentration of the volatile compounds was carried out by extraction with an organic solvent (n-hexane) or solid phase microextraction (SPME). MeHg+ was finally separated and detected by gas chromatography with atomic emission or mass spectrometry detection (GC-MIP-AED or GC-MS). In all the cases the concentrations obtained for MeHg+ in the CRM-580 were significantly higher than the certified value. For the IAEA-405, however, the MeHg+ concentration found was always statistically indistinguishable from the certified value. Experiments were also conducted with synthetic samples, such as aqueous mixtures of MeHg+ and inorganic mercury (Hg2+) or silica-gel spiked with both compounds. The methylation rates found (defined as the percentage of Hg2+ present in the sample which methylates to give artifact MeHg+) ranged from not observable (in certain synthetic aqueous mixtures) to 0.57% (analysis of CRM-580 under certain conditions). As the amount of Hg2+ available in the sample seems to be the main factor controlling the magnitude of the artifact, several experiments were conducted using an ionic exchange resin (Dowex M-41) in order to minimise the concentration of this chemical in the reaction medium. First, a hydrochloric leachate of the sample was passed through a microcolumn packed with the exchanger. Second, the resin was mixed with the sample prior to extraction with HCl. In both cases, the predominant Hg2+ species, HgCl42−, was adsorbed on the resin, whereas MeHg+, mainly as MeHgCl, remained in solution. Following the second option, a new method to analyse MeHg+ in conflictive matrices like certain sediments was proposed. This approach produced better results for the CRM-580, but a MeHg+ concentration slightly, but statistically significant, higher than the reference value was still obtained. 相似文献
9.
Zabaljauregui M Delgado A Usobiaga A Zuloaga O de Diego A Madariaga JM 《Journal of chromatography. A》2007,1148(1):78-85
A simple, fast, and accurate method for the simultaneous determination of methylmercury (MeHg(+)), monobutyltin (MBT), dibutyltin (DBT) and tributyltin (TBT) in seafood is proposed. The method makes use of relatively cheap instrumentation and allows simultaneous analysis of those four species in a routine basis. The sample is treated with methanolic potassium hydroxide in an ultrasound bath, derivatised with sodium tetraethylborate (NaBEt(4)), preconcentrated into n-hexane and analysed by gas chromatography with atomic emission detection (GC-MIP/AES). The soft extraction conditions provided by ultrasound energy prevent chemical decomposition of the analytes and allow fast and efficient recovery of the species considered. Both the extraction and the derivatisation/preconcentration steps were optimised. Detection limits of 34, 3, 6 and 8 ng g(-1) (dry mass) were obtained for MeHg(+), MBT, DBT and TBT, respectively, using the best experimental conditions found. The uncertainty of the analysis ranged from 11% (MeHg(+)) to 15% (MBT). The accuracy of the method was checked by the analysis of several certified reference materials, e.g., BCR 477 (mussel tissue, MBT, DBT and TBT), DOLT-2 (dogfish liver, MeHg(+)), BCR 463 (tuna fish, MeHg(+)) and NIST 2976 (mussel tissue, MeHg(+)) with satisfactory results. Several oyster samples collected in the estuary of the Oka River (Urdaibai, Unesco Reserve of the Biosphere, Basque Country) during four sampling campaigns in 2003-2004 were processed following the proposed procedure. Concentrations ranging from 65 to 149 ng g(-1) (MeHg(+)), 相似文献
10.
Ion‐Pair SN2 Reaction of OH− and CH3Cl: Activation Strain Analyses of Counterion and Solvent Effects 下载免费PDF全文
Jalal Z. A. Laloo Dr. Lydia Rhyman Dr. Olatz Larrañaga Prof. Dr. Ponnadurai Ramasami Prof. Dr. F. Matthias Bickelhaupt Dr. Abel de Cózar 《化学:亚洲杂志》2018,13(9):1138-1147
We have theoretically studied the non‐identity SN2 reactions of MnOH(n?1)+CH3Cl (M+=Li+, Na+, K+, and MgCl+; n=0, 1) in the gas phase and in THF solution at the OLYP/6‐31++G(d,p) level using polarizable continuum model (PCM) implicit solvation. We want to explore and understand the effect of the metal counterion M+ and solvation on the reaction profile and the stereoselectivity of these processes. To this end, we have explored the potential energy surfaces of the backside (SN2‐b) and frontside (SN2‐f) pathways. To explain the computed trends, we have carried out analyses with an extended activation strain model (ASM) of chemical reactivity that includes the treatment of solvation effects. 相似文献