Mathematical Correction for Polyatomic Isobaric Spectral Interferences in Determination of Lanthanides by Inductively Coupled Plasma Mass Spectrometry

The determination of lanthanides by Inductively Coupled Plasma Mass Spectrometry (ICP‐MS) is complicated by several spectral overlaps from M⁺, MO⁺ or MOH⁺ ions formed in the ICP. Especially, it is essential to avoid the spectral interferences from lighter lanthanide and Ba polyatomic ions on middle or heavier lanthanides. To tackle this problem, we have developed a mathematical correction method, which reduces all the spectral overlaps from oxide species of Pr, Nd, Ce and Sm over Gd, Tb, Dy and Ho, and Gd, Tb over Yb and Lu. It can also successfully correct the oxide and hydroxide interference of Ba over Eu. The effectiveness of the proposed the mathematical correction scheme is demonstrated for the USGS Standard Rock samples AGV‐1 and G‐2. The results show that the experimental data obtained by applying the mathematical correction scheme for lanthanides is in good agreement with the reported values, using pneumatic and ultrasonic nebulisation methods, for their ICP‐MS analysis.     

7-(2-Methoxycarbonylvinyl)-3-hydroxychromones: new dyes with red shifted dual emission

7-(2-Methoxycarbonylvinyl)-3-hydroxychromones have been synthesized using Heck coupling reaction from the corresponding 7-bromo-3-hydroxychromones. Introduction of the electron acceptor (2-methoxycarbonylvinyl) group at 7-position of 3-hydroxychromone results in a 30-40 nm red shift in absorption and >50 nm red shifts of both bands in emission. This derivatization allowed us to develop dyes with absorption maxima reaching 480 nm and dual emission in the red region of the spectrum. In comparison to the parent dyes, 7-acryl-3-hydroxychromones demonstrate significantly stronger solvatochromism. This is due to the acceptor group at 7-position, which increases the transfer character of the excited state of the dyes. The new dyes are highly prospective for the development of new fluorescent probes in biological research.     

Theoretical study of the reaction of alkynes with furan catalyzed by AuCl3 and AuCl

A general scheme for the endo‐ and exo‐cyclization of furan reactivity with [L ‐Au^{III, I}Cl_x] with (x = 3, 1 and L ‐acetylene and vinylidene) complexes is investigated using density functional theory (DFT) code. Two conceivable mechanisms via a [4 + 2] Diels–Alder process or carbene complex are analyzed. According to the activation energy values of the gold (III and I) catalyst, the first mechanism, which implies the Diels–Alder reaction of Au^III, is thermodynamically favored and gives more evidence of the intramolecular addition of the furan with the alkynes. The second mechanism, presumably assisted by the spontaneous formation of the exo‐vinylidene complexes and intermediates of gold (III, I) by forming the carbene complex, is kinetically favored. Additionally, we compare our results with other structures with intramolecular additions that exhibit the quasi‐similarity of gold analogue structures. Differences in activation energies are observed, according to the functional used. Finally, we probe the solvent effects, which decrease the energy barrier in the path. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007     

Water‐Soluble N‐(n‐Fatty acyl)chitosans

Chitosan was partially N‐acylated by treatment with n‐fatty acid anhydrides in a homogeneous solution in 2 vol.‐% aqueous acetic acid‐methanol (1:2 v/v). The degree of substitution (d.s.) for N‐acyl groups in the water‐soluble N‐acylchitosan derivatives was in the range of 0.42–0.82 for N‐acetyl, 0.37–0.76 for N‐propionyl, 0.52–0.71 for N‐butyryl and 0.54–0.64 for N‐pentanoyl and ca. 0.58 for N‐hexanoyl, respectively.

Water soluble N‐(n‐fatty acyl)chitosans.     

Pure Organic Phase Phenol Biosensor Based on Tyrosinase Entrapped in a Vapor Deposited Titania Sol‐Gel Membrane

A novel amperometric biosensor was constructed for the determination of phenols in pure organic phase. This biosensor was fabricated by immobilizing tyrosinase in a titania sol‐gel membrane which was obtained with a vapor deposition method. This method was facile and avoided the calcination step needed in conventional titania sol‐gel process. The titania sol‐gel membrane could effectively retain the essential water layer around the enzyme molecule needed for maintaining its activity in organic phase. The experimental parameters such as solvent and operating potential were optimized. At ?100 mV this biosensor showed a good amperometric response to phenols in pure chloroform without any mediator and rehydration of the enzyme. For catechol determination the sensor exhibited a fast response of less than 5 seconds. The sensitivity of different phenols was as follows: catechol > phenol > p‐cresol. Additionally, the apparent Michaelis‐Menten constants of the encapsulated tyrosinase to catechol, phenol and p‐cresol were found to be 0.15±0.003, 0.17±0.008 and 0.21±0.004 mM, respectively. The biosensor had also good reproducibility and stability. This work provided a promising platform for the construction of pure organic phase biosensors and the determination of substrates with poor water solubility.     

Analysis of highly resolved x‐ray photoelectron Cr 2p spectra obtained with a Cr2O3 powder sample prepared with adhesive tape

By using modern XPS systems it is possible to obtain spectra with well‐resolved spin orbit, multiplet and field splitting even with powder samples mounted using adhesive tape. Measurement of Cr₂O₃ powder with the latest generation of XPS spectrometers, which are able to analyse non‐conductive powders with ultimate energy resolution, revealed multiplet splitting features and satellite emission in the Cr 2p spectrum. Therefore, peak‐fit analysis of Cr 2p XPS spectra of Cr(III) compounds requires a more appropriate approach and common practice has to be reconsidered. One possible way to analyse this spectrum is proposed, based on the experimental and theoretical work of other authors. Copyright © 2004 John Wiley & Sons, Ltd.     

Randomized algorithms for the separation of point sets and for solving quadratic programs

A randomized algorithm for finding a hyperplane separating two finite point sets in the Euclidean space ^d and a randomized algorithm for solving linearly constrained general convex quadratic problems are proposed. The expected running time of the separating algorithm isO(dd! (m + n)), wherem andn are cardinalities of sets to be separated. The expected running time of the algorithm for solving quadratic problems isO(dd! s) wheres is the number of inequality constraints. These algorithms are based on the ideas of Seidel's linear programming algorithm [6]. They are closely related to algorithms of [8], [2], and [9] and belong to an abstract class of algorithms investigated in [1]. The algorithm for solving quadratic problems has some features of the one proposed in [7].This research was done when the author was supported by the Alexander von Humboldt Foundation, Germany.On leave from the Institute of Mathematics and Mechanics, Ural Department of the Russian Academy of Sciences, 620219 Ekaterinburg, S. Kovalevskaya str. 16, Russia.     

X-ray emission spectroscopy with EPMA applied to high Tc Superconductors using new spectrometer crystals

The High Temperature Superconductors are characterized by a very anisotropical structure and by typical arrangements of Cu- and O-atoms within CuO₂-planes. In studying the electronic structure of these compounds there is a strong demand for high resolution valence band spectroscopy. Using an electron probe microanalyzer we study the X-ray emission of O-K_ga and Cu-L emerging from polycrystalline YBa₂Cu₃O₇ and Tl₂Ba₂Ca₂Cu₃O₁₀. The O-K emission band is analyzed using a chlinochlore crystal in (001) orientation (2d = 28.4 Å). For the Cu-L emission band we use a beryl crystal in (10¯10) orientation (2d = 15.9 Å). Furthermore, orientation dependent X-ray emission spectroscopy of single-crystalline YBa₂Cu₃O₇ and Tl₂Ba₂Ca₁Cu₂O₈ specimens was performed. We present the partial O-K spectra which represent the O-2p ( = x, y, z) electronic densities of states of the valence band and compare them with calculated data.     

钾原子中多种受激辐射参与的混频过程

当双原子共振激发钾原子于６Ｓ能级时,由光泵受激辐射和电离复合受激辐射参与的六波或四波混频,产生了位于紫外和紫区的诸多相干辐射、文中对多种混频机制进行了分析和讨论,并对所测得的相干辐射线进行了标识．     

Polarized emission from a rhenium metal-ligand complex

We report the first observation of polarized emission from a rhenium-phenanthroline complex, Re(CO)₃(phen)Cl. Highly luminescent rhenium complexes are known, with quantum yields near 0.5 and lifetimes in excess of 10 s. The detection of polarized emission suggests the use of rhenium complexes as probes of the hydrodynamics of large macromolecular complexes and for use in fluorescence polarization immunoassays with gated detection.