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41.
Analysis of acrylamide in food by isotope-dilution liquid chromatography coupled with electrospray ionization tandem mass spectrometry 总被引:1,自引:0,他引:1
A confirmatory method for the determination of low levels of acrylamide in different food products is presented. The method entails extraction of acrylamide with water, precipitation of matrix constituents with acetonitrile, and two clean-up steps consecutively over Isolute Multimode and cation-exchange cartridges. The final extract is analyzed by liquid chromatography (LC) coupled to positive electrospray ionization tandem mass spectrometry employing [13C3]-acrylamide as internal standard. For the chromatographic step, a LC column based on a polymethacrylate gel is employed which shows good retention of acrylamide under isocratic flow conditions (k' = 1.2). Mass spectral acquisition is done by selected reaction monitoring, choosing the characteristic transitions m/z 72-->55, 72-->54 and 72-->27. In-house validation data for breakfast cereals and crackers show good precision of the method, with intra- and interassay variation below 10%. The limits of detection for crackers and breakfast cereals, respectively are estimated at 15 and 20 microg/kg, and recoveries of fortified samples ranged between 58 and 76%. Furthermore, the method is applicable to a number of different food products, including biscuits, crisp bread, wafers, confectionery cocoa liquor, and nuts. Finally, the good results obtained in several small-scale interlaboratory tests provided additional confidence in the performance of the method. 相似文献
42.
Micro- and nanotubes of an amorphous carbon nitride material were synthesized by metathesis reactions between cyanuric chloride (C3N3Cl3) and different nitrogen sources, such as Li2(CN2) or Li3(BN2). The intermediate formation of needle-shaped crystals of N(C3N3Cl2)3 was always observed in our reactions, and investigated with respect to their role as a template in the formation of tubes. Chemical analyses of the micro- and nanotubes reveal carbon to nitrogen ratios near 3:4, consistent with the suspected material C3N4. Synthesized carbon nitride materials were thermally stable up to 600 °C in inert atmosphere. They were inspected by a number of physical measurements, mainly using TEM, EDX and IR investigations. 相似文献
43.
44.
Wissdorf W Pohler L Klee S Müller D Benter T 《Journal of the American Society for Mass Spectrometry》2012,23(2):397-406
Results obtained with two computational approaches for the simulation of ion motion at elevated pressure are compared with
experimentally derived ion current data. The computational approaches used are charged particle tracings with the software
package SIMION ver. 8 and finite element based calculations using the software package Comsol Multiphysics ver. 4.0/4.0a.
The experimental setup consisted of a tubular corona discharge ion source coupled to a cylindrical measurement chamber held
at atmospheric pressure. Generated ions are flown into the chamber at essentially subsonic laminar isothermal conditions.
In the simulations, strictly stationary conditions were assumed. The results show very good agreement between the SIMION/SDS
model and experimental data. For the Comsol model, only qualitative agreement is observed. 相似文献
45.
Dr. Sonja Pullen Dr. Alexander Hegmans Prof. Wolf G. Hiller André Platzek Prof. Eva Freisinger Prof. Bernhard Lippert 《ChemistryOpen》2021,10(1):28-45
The conversion of the 1 : 1-complex of Cisplatin with 1-methyluracil (1MeUH), cis-[Pt(NH3)2(1MeU-N3)Cl] ( 1 a ) to the aqua species cis-[Pt(NH3)2(1MeU-N3)(OH2)]+ ( 1 b ), achieved by reaction of 1 a with AgNO3 in water, affords a mixture of compounds, the composition of which strongly depends on sample history. The complexity stems from variations in condensation patterns and partial loss of NH3 ligands. In dilute aqueous solution, 1 a , and dinuclear compounds cis-[(NH3)2(1MeU-N3)Pt(μ-OH)Pt(1MeU-N3)(NH3)2]+( 3 ) as well as head-tail cis-[Pt2(NH3)4(μ-1MeU-N3,O4)2]2+ ( 4 ) represent the major components. In addition, there are numerous other species present in minor quantities, which differ in metal nuclearity, stoichiometry, stereoisomerism, and Pt oxidation state, as revealed by a combination of 1H NMR and ESI-MS spectroscopy. Their composition appears not to be the consequence of a unique and repeating coordination pattern of the 1MeU ligand in oligomers but rather the coexistence of distinctly different condensation patterns, which include μ-OH, μ-1MeU, and μ-NH2 bridging and combinations thereof. Consequently, the products obtained should, in total, be defined as a heterogeneous mixture rather than a mixture of oligomers of different sizes. In addition, a N2 complex, [Pt(NH3)(1MeU)(N2)]+ appears to be formed in gas phase during the ESI-MS experiment. In the presence of Na+ ions, multimers n of 1 a with n=2, 3, 4 are formed that represent analogues of non-metalated uracil quartets found in tetrastranded RNA. 相似文献
46.
Neven Cukrov Nataša Tepić Dario Omanović Sonja Lojen Elvira Bura-Nakić Vjeročka Vojvodić 《International journal of environmental analytical chemistry》2013,93(10):1187-1199
Multivariate statistical analyses were applied on the measured physico-chemical (Cd, Pb, Cu, Zn, Mg, Ca, O2, alkalinity, temperature, pH, SAS, DOC and DIC) and isotopic parameters (δ13C and δ18O) to estimate and distinguish anthropogenic from natural influences to the water system of the Krka River. Analyses were conducted on the data collected during six years from twelve sampling sites. On the basis of orientation, positioning and grouping of parameters arranged by biplots, four main hypotheses were defined and finally statistically confirmed. Thereof, two main and distinct processes occurring in the Krka River could be highlighted: (i) upstream pollution, caused by the inflow of untreated waste-waters of city of Knin and (ii) downstream self-purification, caused by the sedimentation and/or co-precipitation of pollutants coupled by the inflow of clean subterranean water (groundwater recharge). Grouping of (i) hydrological and carbon cycle connected parameters, and (ii) anthropogenically influenced correlated parameters were proposed as a result of statistical analysis. Regarding the pH, it is shown that a stream section influenced by the subterranean inflow of Zrmanja River is statistically significantly different for all sampling campaigns during six years, being lower for about 0.5 pH unit. 相似文献
47.
Peez Nadine Becker Jochen Ehlers Sonja M. Fritz Melanie Fischer Christian B. Koop Jochen H. E. Winkelmann Carola Imhof Wolfgang 《Analytical and bioanalytical chemistry》2019,411(28):7603-7603
Analytical and Bioanalytical Chemistry - The original version of this article contained a mistake. 相似文献
48.
Markus Weiß Sonja Borchert Emmanuelle Rmond Sylvain Jug Harald Grger 《Heteroatom Chemistry》2012,23(2):202-209
A proof of concept for the asymmetric organocatalytic aza‐Michael addition reaction of nitrogen nucleophiles with simple and readily available alkyl enoates as acceptor molecules in the presence of a chiral phase‐transfer catalyst has been demonstrated. The desired enantiomerically enriched β‐amino acid derivatives were obtained in up to 86% yield and with enantioselectivities of up to 37% ee. © 2012 Wiley Periodicals, Inc. Heteroatom Chem 23:202–209, 2012; View this article online at wileyonlinelibrary.com . DOI 10.1002/hc.21004 相似文献
49.
Sebastian Enck Peter Tremmel Sonja Eckhardt Michael Marsch Armin Geyer 《Tetrahedron》2012,68(35):7166-7178
We present the stereoselective synthesis of various highly functionalized thiazole dipeptides that are found in thiopeptide antibiotics like thiazomycins and nocathiacins. The condensation of an uronic acid with l-cysteine methyl ester delivers along two different protocols the stereopure thiazolidine lactones or lactams on the multigram scale, respectively. Oxidation of the thiazolidine moiety to the thiazole and tailoring of the sugar chains yield the thiazole dipeptide as present in the core motif of the thiopeptide antibiotics, as well as its epimer and a homolog. The modular assembly of the potent natural products and their analogs relies on the synthetic accessibility of adequately protected building blocks of tailored absolute stereochemistry. 相似文献
50.
Employing a cleavable carbohydrate–peptide linker, a new strategy for single-bead analysis of multivalent cyclic neoglycopeptides based on Edman degradation is described. Edman degradation of glycopeptides is hampered by the acid lability of the glycosidic bond and potential incompatibilities of phenylthiohydantoin (PTH) derivatives of glycosylated amino acids with PTH derivatives of the proteinogenic amino acids. To overcome this problem, carbohydrates are detached from the cyclopeptide templates before single-bead analysis, allowing for micro sequencing under routine conditions. With this strategy, application of multivalent cyclic neoglycopeptides in split-mix libraries with a subsequent screening process becomes possible for the first time. 相似文献