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31.
Sanchiz J Esparza P Villagra D Domínguez S Mederos A Brito F Araujo L Sánchez A Arrieta JM 《Inorganic chemistry》2002,41(23):6048-6055
The coordinating ability of the ligands 3,4-toluenediamine-N,N,N',N'-tetraacetate (3,4-TDTA), o-phenylenediamine-N,N,N',N'-tetraacetate (o-PhDTA), and 4-chloro-1,2-phenylenediamine-N,N,N',N'-tetraacetate (4-Cl-o-PhDTA) (H4L acids) toward lead(II) is studied by potentiometry (25 degrees C, I = 0.5 mol x dm(-3) in NaClO4), UV-vis spectrophotometry, and 207Pb NMR spectrometry. The stability constants of the complex species formed were determined. X-ray diffraction structural analysis of the complex [Pb4(mu-3,4-TDTA)4(H2O)2]*4H2O (1) revealed that 1 has a 2-D structure. The layers are built up by the polymerization of centrosymmetric [Pb4L2(H2O)2] tetranuclear units. The neutral layers have the aromatic rings of the ligands pointing to the periphery, whereas the metallic ions are located in the central part of the layers. In compound 1, two types of six-coordinate lead(II) environments are produced. The Pb(1) is coordinated to two nitrogen atoms and four carboxylate oxygens from the ligand, whereas Pb(2) has an O6 trigonally distorted octahedral surrounding. The lead(II) ion is surrounded by five carboxylate oxygens and a water molecule. The carboxylate oxygens belong to four different ligands that are also joined to four other Pb(1) ions. The selective uptake of lead(II) was analyzed by means of chemical speciation diagrams as well as the so-called conditional or effective formation constants K(Pb)eff. The results indicate that, in competition with other ligands that are strong complexing agents for lead(II), our ligands are better sequestering agents in acidic media. 相似文献
32.
J. Doménech E. Brillas J. A. Garrido R. M. Rodríguez 《Monatshefte für Chemie / Chemical Monthly》1987,118(2):197-202
Viscosities and densities of lithium perchlorate solutions in different ethylene glycol-water compositions have been measured at 25.0 and 35.0 °C. From these data, the correspondingB-coefficients of theJones-Dole equation have been determined. TheB-value depends on the solvent composition and it reaches a maximum in the water-rich region. This behaviour is analysed in terms of ionic solvation and solvent structure.
Viskositäts-B-Koeffizienten für Lösungen von Lithiumperchlorat in Ethylenglykol-Wasser-Mischungen
Zusammenfassung Es wurden die Dichten und Viskositäten für Lösungen von Lithiumperchlorat in verschieden zusammengesetzten Ethylenglykol-Wasser-Mischungen bei 25 °C und 35 °C gemessen. Auf Grund der erhaltenen Daten wurden dieB-Koeffizienten in den entsprechendenJones-Dole-Gleichungen für die relative Viskosität bestimmt. DieB-Werte hängen von der Zusammensetzung des Lösungsmittels ab und erreichen im wasserreichen Konzentrationsgebiet ein Maximum. Dieses Verhalten wird in Hinblick auf die Ionensolvatation und die Struktur des Lösungsmittels analysiert.相似文献
33.
Domínguez-González R Moreda-Piñeiro A Bermejo-Barrera A Bermejo-Barrera P 《Talanta》2005,66(4):937-942
A new method using diluted reagents (nitric and hydrochloric acids and oxygen peroxide) and ultrasound energy to assist metals acid leaching with from edible seaweed was optimized. The method uses a first sonication at high temperature with hydrochloric acid as a previous stage to an ultrasound-assisted acid leaching with 7 ml of an acid solution containing nitric acid, hydrochloric acid and hydrogen peroxide at concentrations of 3.7, 3.0 and 3.0 M, respectively. Optimum conditions for the first sonication step were ultrasound energy at 17 kHz, sonication temperature at 65 °C, an acid volume of 2 ml, an hydrochloric acid concentration of 6.0 M and a sonication time of 10 min. It has been found that the first sonication stage at high temperature with hydrochloric acid is necessary to obtain quantitative recoveries for As, Ba, Fe and V. Otherwise quantitative recoveries were reached for the other elements investigated (Ca, K, Na, Mg, Cd, Cr, Cu, Mn, Ni, Pb and Zn). The repeatability of the ultrasound-assisted acid leaching method was around 10% for all elements. Adequate limit of detection and limit of quantification were reached by using inductively coupled plasma-optical emission spectrometry (ICP-OES) for measurements. The method resulted accurate after analysing several seaweed certified reference materials (IAEA-140/TM, NIES-03 and NIES-09). The method was finally applied to the multi-element determination in edible seaweed samples. 相似文献
34.
Doménech-Carbó A Doménech-Carbó MT Saurí-Peris MC Gimeno-Adelantado JV Bosch-Reig F 《Analytical and bioanalytical chemistry》2003,375(8):1169-1175
An electrochemical method for identifying anthraquinone-type dyes in microsamples from works of art, based in the voltammetry of microparticles approach, is reported. Upon attachment onto graphite/polyester composite electrodes, natural pigments aloe, henna, cochineal red, madder lake, kermes, shellac, and alizarin and purpurin taken as reference materials can be identified from their square wave voltammetric profiles in MeCN (0.10 mol L(-1) Bu(4)NPF(6)) and aqueous (0.25 mol L(-1) acetic acid+0.25 mol L(-1) sodium acetate) electrolytes. 相似文献
35.
36.
Emilio J. González Patricia F. Requejo Ángeles Domínguez Eugénia A. Macedo 《Journal of solution chemistry》2013,42(4):746-763
In this study, densities and speeds of sound were measured over the whole composition range, at T = (298.15, 303.15 and 308.15) K and p = 0.1 MPa, for the binary systems of ethanol, or 1-propanol, or 2-propanol and 1-butyl-3-methylpyridinium bis(trifluoromethylsulfonyl)imide, or 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide. The density and speed of sound data were used to calculate the corresponding excess molar volumes and excess molar isentropic compressions, which were fitted with the Redlich–Kister equation. From the obtained results, a discussion was carried out in terms of interactions and structure factors in these binary mixtures. 相似文献
37.
José Luis Doménech 《Molecular physics》2017,115(13):1465-1466
In a recent article, Y. Liu, X. Cheng, H. Cheng, J. Cheng and X. Song [Mol. Phys., 114:19, 2817–2823] report on the calculation of potential energy curves and the derivation of spectroscopic constants and line intensities for the lowest energy electronic states of HCl+. There are several shortcomings in the article; the most notable being the incorrect ordering of the 2П3/2 and 2П1/2 state energies, erroneous selection rules, which lead to the absence of a Q-branch in their predicted spectra, incorrect Höln–London factors, and a missing appendix. 相似文献
38.
39.
S. Domínguez O. García M. Ezquer M.J. Rodríguez A.R. Lagunas J. Pérez-Conde J. Bravo 《Photonics and Nanostructures》2012,10(1):46-53
This paper presents a process to easily fabricate photonic crystals (PCs) on silicon to increase the efficiency of solar cells by reducing the sunlight reflection in the front surface of the cell. The process, based on laser interference lithography (LIL) and reactive ion etching (RIE), allows creating nanostructures over large areas with different shapes and dimensions. The reflectance of the resulting surface depends on the height, pitch, width and shape of the created PC. In this work, these parameters have been optimized by computer simulation and the best PC so far found has been fabricated on silicon. We obtain a normal reflectance under 10% in the spectral region between 500 and 900 nm without any other material employed as antireflecting coating. 相似文献
40.
Zaira Domínguez Javier Hernández Lorena Silva-Gutiérrez Magali Salas-Reyes Mario Sánchez Gabriel Merino 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4):772-784
The effect of electron-withdrawing (EW) and electron-releasing (ER) substituents on the 31P NMR chemical shifts and the structural parameters of a series of tris-(p-X-aryl)selenophosphates is reported in this article. Similarly to O-aryl phosphates and O-aryl thiophosphates, EW groups attached to aromatic rings induce a shielding effect on the 31P NMR signal. After a detailed experimental and theoretical analysis, we confirmed that the selenium atom is the main part responsible for the charge density transfer toward phosphorus through a back-bonding effect. The obtained 1JP-Se values for the complete series agree with this observation. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献