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Eva Kanso 《Theoretical and Computational Fluid Dynamics》2010,24(1-4):201-207
We present a set of equations governing the motion of a body due to prescribed shape changes in an inviscid, planar fluid with nonzero vorticity. The derived equations, when neglecting vorticity, reduce to the model developed in Kanso et al. (J Nonlinear Sci 15:255–289, 2005) for swimming in potential flow, and are also consistent with the models developed in Borisov et al. (J Math Phys 48:1–9, 2007), Kanso and Oskouei (J Fluid Mech 800:77–94, 2008), Shasikanth et al. (Phys Fluids 14(3):1214–1227, 2002) for a rigid body interacting dynamically with point vortices. The effects of cyclic shape changes and the presence of vorticity on the locomotion of a submerged body are discussed through examples. 相似文献
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Eva Greibe Magnus Leth-Møller Sofie Stampe Per Ovesen Michael Pedersen Elke Hoffmann-Lücke 《Biomedical chromatography : BMC》2022,36(6):e5350
Artificial sweeteners are widely used as substitutes for sugar. The sweeteners are generally considered safe, however their whereabouts during pregnancy and lactation and the effect on child development are poorly explored. There is a need for new tools to measure these substances during pregnancy and lactation. Here, we describe the development and validation of a sensitive liquid chromatography–tandem mass spectrometry method for the simultaneous quantification of acesulfame, cyclamate, saccharin and sucralose in human plasma, umbilical cord blood, amniotic fluid and breast milk. The samples were prepared by protein precipitation and separated on a Luna Omega Polar C18 column (2.1 × 50 mm, 1.6 μm). Electrospray ionization in negative mode and multiple reaction monitoring were used to monitor the ion transitions. The validated concentration ranges were from 1 to 500 ng/ml (10–500 ng/ml for sucralose). Interassay precisions were all ≤15% and the accuracies were within ±15%. Stability, linearity, dilution integrity, carryover and recovery were also examined and satisfied the validation criteria. Finally, this analytical method was successfully applied on spiked samples of plasma, umbilical cord blood, amniotic fluid and breast milk, proving its suitability for use in clinical studies on artificial sweeteners, including during pregnancy and lactation. 相似文献
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Vrbková Eva Sekerová Lada Vyskočilová Eliška Zapletal Martin Červený Libor 《Research on Chemical Intermediates》2022,48(4):1403-1421
Research on Chemical Intermediates - Several types of modified zeolite BETA38 with different iron loading were prepared. Prepared materials were characterized using different techniques (XRD, XRF,... 相似文献
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Neil R. Judge Dr. Leonie J. Bole Prof. Eva Hevia 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(10):e202104164
Advancing the understanding of using alkali-metal alkoxides as additives to organomagnesium reagents in Mg−Br exchange reactions, a homologous series of mixed-ligand alkyl/alkoxide alkali-metal magnesiates [MMg(CH2SiMe3)2(dmem)]2 [dmem=2-{[2-(dimethylamino)ethyl]methylamino} ethoxide; M=Li, 1 ; Na, 2 ; (THF)K, 3 ] has been prepared. Structural and spectroscopic studies have established the constitutions of these heteroleptic/heterometallic species, which are retained in arene solution. Evaluation of their reactivity towards 2-bromoanisole has uncovered a marked alkali-metal effect with potassium magnesiate 3 being the most efficient of the three ate reagents. Studies probing the constitution of the exchange product from this reaction suggest that the putative [KMgAr2(dmem)]2 (Ar=o-OMe−C6H4) intermediate undergoes redistribution into its single metal components [KAr]n and [MgAr(dmem)]2 ( 5 ). This process can be circumvented by using a different potassium alkoxide containing an aliphatic chain such as KOR’ (R’=2-ethylhexyl) which undergoes co-complexation with Mg(CH2SiMe3) to give [KMg(CH2SiMe3)2(OR’)]2 ( 7 ). This ate, in turn, reacts quantitatively with 2-bromoanisole furnishing [KMgAr2(OR’)]2 ( 9 ) which is stable in solution as a bimetallic compound. Collectively this work highlights the complexity of these alkali-metal mediated Mg−Br exchange reactions, where each reaction component can have a profound effect not only on the success of the reaction; but also the stability of the final metalated intermediates prior to their electrophilic interception. 相似文献
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Dr. Tetiana Pavlovska David Král Lesný Dr. Eva Svobodová Dr. Irena Hoskovcová Dr. Nataliya Archipowa Dr. Roger Jan Kutta Prof. Dr. Radek Cibulka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(46):e202200768
Deazaflavins are well suited for reductive chemistry acting via a consecutive photo-induced electron transfer, in which their triplet state and semiquinone – the latter is formed from the former after electron transfer from a sacrificial electron donor – are key intermediates. Guided by mechanistic investigations aiming to increase intersystem crossing by the internal heavy atom effect and optimising the concentration conditions to avoid unproductive excited singlet reactions, we synthesised 5-aryldeazaflavins with Br or Cl substituents on different structural positions via a three-component reaction. Bromination of the deazaisoalloxazine core leads to almost 100 % triplet yield but causes photo-instability and enhances unproductive side reactions. Bromine on the 5-phenyl group in ortho position does not affect the photostability, increases the triplet yield, and allows its efficient usage in the photocatalytic dehalogenation of bromo- and chloroarenes with electron-donating methoxy and alkyl groups even under aerobic conditions. Reductive powers comparable to lithium are achieved. 相似文献
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Dr. Gerd M. Ballmann Dr. Thomas X. Gentner Dr. Alan R. Kennedy Prof. Dr. Eva Hevia Prof. Dr. Robert E. Mulvey 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(55):e202201716
Rare examples of heavier alkali metal manganates [{(AM)Mn(CH2SiMe3)(N‘Ar)2}∞] (AM=K, Rb, or Cs) [N‘Ar=N(SiMe3)(Dipp), where Dipp=2,6-iPr2-C6H3] have been synthesised with the Rb and Cs examples crystallographically characterised. These heaviest manganates crystallise as polymeric zig-zag chains propagated by AM⋅⋅⋅π-arene interactions. Key to their preparation is to avoid Lewis base donor solvents. In contrast, using multidentate nitrogen donors encourages ligand scrambling leading to redistribution of these bimetallic manganate compounds into their corresponding homometallic species as witnessed for the complete Li - Cs series. Adding to the few known crystallographically characterised unsolvated and solvated rubidium and caesium s-block metal amides, six new derivatives ([{AM(N‘Ar)}∞], [{AM(N‘Ar)⋅TMEDA}∞], and [{AM(N‘Ar)⋅PMDETA}∞] where AM=Rb or Cs) have been structurally authenticated. Utilising monodentate diethyl ether as a donor, it was also possible to isolate and crystallographically characterise sodium manganate [(Et2O)2Na(nBu)Mn[(N‘Ar)2], a monomeric, dinuclear structure prevented from aggregating by two blocking ether ligands bound to sodium. 相似文献
60.
This work demonstrates the analytical applicability of single ion-selective membranes (ISMs) and potentiometric sensor array to distinguish and detect cathinone derivatives. Potentiometric data from ISMs based on cation exchanger and varying content of calix[4]arene derivative were processed by principal component analysis (PCA). Such a combination of methods allowed discriminating various individual synthetic cathinones and their recognition from the mixture comprising primary amines (substituted amphetamines+aminoindane). Analytical parameters of ISM containing 1wt % of calix[4]arene derivative were sufficient to detect 1.0×10−4 mol.l−1 1-(4-fluorophenyl)-2-(ethylamino)butan-1-one and 2-(methylamino)-1-phenylbutan-1-one (buphedrone) in both model and saliva samples. 相似文献