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Here we present a novel strategy for the quantification of ascorbic acid (AA) (vitamin C). The developed method is based on the quenching effect produced by AA on the time-resolved luminescence signal of europium ions using excitation and emission wavelengths of 388 nm and 617 nm. The method presents a linear dynamic range from 0.2 to 2 µg mL−1 with a detection limit of 0.06 µg mL−1 and a relative standard deviation lower than 6%. The method was applied to the determination of AA in pharmaceutical preparations, human serum and human urine. The obtained results in pharmaceuticals were compared with a reference method; the recovery yields were close to 100% in all cases. The accuracy of the method was statistically assessed, demonstrating the suitability of this alternative method for the determination of AA in pharmaceuticals and biological samples, requiring no sample treatment except for a dilution step. [ABSTRACT FROM AUTHOR]

The main objectives of this study are to determine the presence of antimony in water stored in polyethylene terephthalate bottles and the influence of temperature and time over the migration levels. For this purpose, Sb determination was carried out in water at different experimental conditions: storage for one to three weeks at 25 to 80 ℃; long-term (six months) storage at room temperature between 16 and 24 ℃ and storage in car during summer which is a common consumer’s habit. In addition, water quality analysis was developed after different time–temperature storage conditions. All the samples at the end of their storage conditions were analyzed by inductively coupled plasma mass spectrometry. The limit of detection and quantification were 0.50 and 0.80 µg/L, respectively. The results for the bottled water stored during six months indicated that the average Sb concentration was 0.332 ± 0.015 µg/L. This value is below the European maximum permissible migration level of 5 µg/L. With regard to the newly bottled water, no Sb was detected at the initial time for all temperatures studied. However, the Sb concentration in water increased with both time and temperature. The levels of Sb started exceeding the European limits when the samples were stored at 60 ℃ for two weeks. [ABSTRACT FROM AUTHOR]

A new D3h-symmetry tris-N-heterocyclic carbene ligand has been prepared and coordinated to iridium and gold. The ligand contains an electron-poor hexaazatriphenylene core; thus, the resulting tris-NHC ligand is a poor electron donor. The tris–Au(i) complex was tested in the hydroamination of terminal alkynes and in the three-component Strecker reaction. [ABSTRACT FROM AUTHOR]

Three different Ir(iii) complexes with pyrene-containing N-heterocyclic carbenes have been prepared and characterized. Two complexes contain a monodentate pyrene-imidazolylidene ligand, and have the formulae [IrCp*Cl2(pyrene-NHC)] and [IrCp*(CO3)(pyrene-NHC)]. The third complex is a dimetallic complex with a pyrene-di-imidazolylidene bridging ligand, with the formula [{IrCp*(CO3)}2(μ-pyrene-di-NHC)]. The catalytic activity of the three complexes was tested in the H/D exchange of organic substrates, and in the β-alkylation of 1-phenylethanol with primary alcohols. In the deuteration of organic substrates, the carbonate complexes are active even in the absence of additives. The dimetallic complex is the most active one in the catalytic coupling of alcohols, a result that may be interpreted as a consequence of the cooperativity between the two metal centres. [ABSTRACT FROM AUTHOR]

A family of cyclometallated Au(iii) and Pt(ii) complexes containing a CNC-pincer ligand (CNC = 2,6-diphenylpyridine) supported by pyrene-based mono- or bis-NHC ligands have been synthesized and characterized, together with the preparation of a Pt–Au hetero-dimetallic complex based on a Y-shaped tris-NHC ligand. The photophysical properties of all the new species and of two related Ru(ii)–arene complexes were studied and compared. Whereas the pyrene-based complexes only exhibit emission in solution, those containing the Y-shaped tris-NHC ligand are only luminescent when dispersed in poly(methyl methacrylate) (PMMA). In particular, the pyrene-based complexes were found to be emissive in the range of 373–440 nm, with quantum yields ranging from 3.1 to 6.3%, and their emission spectra were found to be almost superimposable, pointing to the fluorescent pyrene-centered nature of the emission. This observation suggests that the emission properties of the pyrene fragment may be combined with some of the numerous applications of NHCs as supporting ligands allowing, for instance, the design of biological luminescent agents. [ABSTRACT FROM AUTHOR]

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Copyright of Nefrologia is the property of Revista Nefrologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)