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101.
Gabriella Santoni Dr. Miriam Mba Dr. Marcella Bonchio Dr. William A. Nugent Cristiano Zonta Dr. Giulia Licini Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(2):645-654
The stereoselective oxidation of differently functionalised benzyl phenyl sulfides has been examined by using enantiopure TiIV trialkanolamine complexes. These complexes efficiently catalyse the sulfoxidation with good stereoselectivities. The data highlight the contribution to the stereoselectivity of steric effects and non‐covalent π–π interactions between the aromatic rings of the TiIV complex and those pertaining to the substrates. Enantiomeric excesses have been correlated with the electrostatic potential surfaces (EPS) of the reacting sulfides. The overall study leads to a mechanistic interpretation that explains the stereoselectivity of the system and dissects the role of aromatic and steric interactions in the stereoselective process. 相似文献
102.
We study the well-posedness of a linear control system Σ(A,B,C,D) with unbounded control and observation operators. To this end we associate to our system an operator matrix $\mathcal{A}$ on a product space $\mathcal{X}^{p}$ and call it p-well-posed if $\mathcal{A}$ generates a strongly continuous semigroup on $\mathcal{X}^{p}$ . Our approach is based on the Laplace transform and Fourier multipliers. The results generalize and complement those of Curtain and Weiss (Int. Ser. Numer. Math. vol. 91. Birkhäuser, Basel, 1989), Staffans and Weiss (Trans. Am. Math. Soc. 354:3229–3262, 2002) and are illustrated by a heat equation with boundary control and point observation. 相似文献
103.
Miriam Isabel Seifert 《Extremes》2014,17(2):193-219
An effective approach for studying the asymptotics of bivariate random vectors is to search for the limits of conditional probabilities where the conditioning variable becomes large. In this context, elliptical and related distributions have been extensively investigated. A quite general model was presented by Fougères and Soulier (Limit conditional distributions for bivariate vectors with polar representation in Stochastic Models, 2010), who derived a conditional limit theorem for random vectors (X, Y) with a polar representation R · (u(T), v(T)), where R, T are stochastically independent and R is in the Gumbel max-domain of attraction. We reformulate their assumptions, such that they have a simpler structure, display more clearly the geometry of the curves (u(t), v(t)) and allow us to deduce interesting generalizations into two directions: u has several global maxima instead of only one, the curve (u(t), v(t)) is no longer differentiable, but forms a “cusp”. The latter generalization yields results where only random norming leads to a non-degenerate limit statement. Ideas and results are elucidated by several figures. 相似文献
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Miriam Beneito‐Cambra Virginia Bernabé‐Zafón Ernesto F. Simó‐Alfonso Guillermo Ramis‐Ramos 《Rapid communications in mass spectrometry : RCM》2010,24(14):2093-2100
A new derivatization procedure to increase the sensitivity of electrospray ionization mass spectrometry (ESI‐MS) to non‐ethoxylated and ethoxylated alcohols was investigated. The analytes were oxidized with chromium(VI) oxide and the resulting carboxylic and ethoxy‐carboxylic acids were isolated by extraction with ethyl acetate; the extracts were alkalinized and infused into the ESI‐MS system working in the negative‐ion mode. The yields of the combined oxidation‐extraction were ca. 100% for non‐ethoxylated fatty alcohols dissolved in acetone and they decreased moderately in samples containing increasing amounts of water (e.g., a 75% yield was obtained with 50% water). Ethoxylated alcohols with more than two ethylene oxide units resulted in yields of ca. 60%. Low limits of detection (LODs) were obtained when the procedure was applied to the analysis of body‐care products and cosmetics containing fatty alcohols, e.g., in a varicose‐vein cream, the LODs were 25 µg cetyl alcohol and 7.5 µg stearyl alcohol (detected as palmitic acid and stearic acid, respectively) per gram of sample. High molecular mass alcohols were also detected in seawater after pre‐concentration by solid‐phase extraction. Thus, the proposed method is particularly valuable for use in industrial samples having complex matrices and in environmental samples and it is competitive with other methods for the analysis of trace amounts of fatty alcohols. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
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Henry Holmstrand Maria Unger Daniel Carrizo Per Andersson Örjan Gustafsson 《Rapid communications in mass spectrometry : RCM》2010,24(14):2135-2142
The bromine isotope composition is potentially diagnostic in both degradation monitoring and source apportionment of organobromines in the environment. A method for compound‐specific bromine isotope analysis (δ81Br) based on gas chromatography multiple collector inductively coupled plasma mass spectrometry (GC/ICPMS) was developed for common brominated diaromatic compounds. Brominated diphenyl ethers (BDEs) in Bromkal 70‐5DE, a technical flame‐retardant mixture containing mainly BDEs #47, #99 and #100, were used as test substances, with standard bracketing for the samples achieved through co‐injected monobromobenzene (MBB) with a known δ81Br of ?0.39‰ vs. Standard Mean Ocean Bromine (SMOBr). Three different heated transfer lines were constructed and tested to achieve efficient conduction of the BDEs from the gas chromatograph to the ICPMS instrument. The MBB was analyzed with a precision of 0.4‰ (1 s, n = 18). The precision for BDEs was 1.4–1.8‰ (1 s, n = 10–12 depending on the congener). The lower precision for the BDEs than for MBB may reflect the heat required to prevent condensation of the analytes in ICP torch assembly. The use of an internal standard of similar chemical structure to the analytes alleviates this problem, as illustrated by a difference of 0.3 ± 0.7‰ (1 s, n = 6) between the δ81Br values of co‐injected methoxy BDE‐47 and BDE‐47 extracted from whale blubber. Improvements in precision and accuracy may be achieved by the use of a more efficient heating of the torch assembly in conjunction with a set of internal standards that match the target compounds. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
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We report the chemical modification of polyethylenimine (PEI) by functionalization with dopamine (Do) using glutaraldehyde (Glu) as a linker (PEI‐Glu‐Do). The new polymer was characterized by FT‐IR spectroscopy, by derivative UV‐vis spectroscopy, and Cyclic Voltammetry. The PEI‐Glu‐Do demonstrated to have an important electrocatalytic activity allowing an important decrease in the overvoltages for the oxidation of NADH and a significant increase in its oxidation peaks currents. Different ratios of PEI:Do were assayed and the best response was obtained using PEI : Glu : Do 1 : 2 : 1. The new polymer represents an interesting and promising alternative for the electrochemical quantification of NADH and other analytes of clinical interest, as well as for the development of new electrochemical (bio)sensors. 相似文献