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71.
Vlekken J D'Olieslaeger M Knuyt G Vandervorst W De Schepper L 《Journal of the American Society for Mass Spectrometry》2000,11(7):650-658
In secondary ion mass spectrometry, the detection of MCs+ clusters (with M an element of the specimen) under a Cs bombardment is frequently used for the quantification of major elements. Despite some very good results obtained by this method, some problems still remain. In order to gain some more insight into these problems, the formation mechanism of the MCs+ clusters is investigated using a Monte Carlo model. It is shown that the majority of the constituent particles of the formed clusters are initially first or second neighbor atoms at the surface and that the velocity distribution of the MCs+ clusters becomes broader and peaked at higher velocities with increasing surface binding energy of the M atom. In addition, it is demonstrated that the interaction potential between the M and Cs+ particle has no influence on the velocity distribution of the MCs+ clusters. On the other hand, the cluster formation probability, defined as the probability that a sputtered M and Cs+ particle will form a MCs+ cluster, is extremely sensitive to this interaction potential. It is also shown that the cluster formation probability decreases with increasing surface binding energy. Finally, a good correspondence is obtained between the calculated and experimental velocity distributions of MCs+ clusters sputtered from different monoatomic materials. As a consequence, the Monte Carlo model and the discussed results can be validated. 相似文献
72.
Andreoli R Manini P Poli D Bergamaschi E Mutti A Niessen WM 《Analytical and bioanalytical chemistry》2004,378(4):987-994
A new and simple method for the determination of fat-soluble vitamins (retinol, alpha-tocopherol, and beta-carotene) in human serum was developed and validated by using liquid chromatography-tandem mass spectrometry with atmospheric pressure chemical ionization (LC-APCI-MS-MS). Different solvent mixtures were tested to obtain deproteinization and extraction of the analytes from the matrix. As a result, a volume of 240 microL of a 1:1 (v/v) ethanol/ethyl acetate mixture added to 60 microL of serum was found to be suitable for both protein precipitation and antioxidants solubilization, giving the best recovery for all three analytes. Deproteinized samples (20 microL) were injected after dilution, without the need for concentration or evaporation to dryness and reconstruction of the sample. Vitamins were separated on a C-8 column using a 95:5 (v/v) methanol/dichloromethane mixture and ionized in the positive-ion mode; detection was performed in the selected-reaction monitoring mode. Linearity of the LC-APCI-MS-MS method was established over 5 orders of magnitude for retinol and alpha-tocopherol, whereas in the case of beta-carotene it was limited to 4 orders. Lower limits of quantitation were 1.7, 2.3, and 4.1 nM for retinol, alpha-tocopherol, and beta-carotene, respectively. Serum concentrations of retinol, alpha-tocopherol, and alpha+beta-carotene determined in a group of healthy volunteers were 2.48, 38.07, and 0.50 microM, respectively, in samples collected in winter ( n=122) and 2.69, 45.88, and 0.90 microM during summer ( n=66). 相似文献
73.
Martha CT van Zeist WJ Bickelhaupt FM Irth H Niessen WM 《Journal of mass spectrometry : JMS》2010,45(11):1332-1343
Ferrocene is a popular template in material science due to its exceptional characteristics that offer the ability to optimize the selectivity and activity of catalysts by the addition of carefully selected substituents. In combinatorial catalyst development, the high susceptibility to electrophilic substitution reactions offers the opportunity for the rapid introduction of molecular diversity. Mass spectrometry (MS)-based continuous-flow systems can be applied to rapidly evaluate catalyst performance as well as to (provisionally) identify the introduced catalyst complexes. Herein, we describe the fragmentation characteristics of the [ferrocenyl bidentate + Ag](+) catalyst complexes in dedicated (high-resolution) MS(n) experiments. The investigation of the fragmentation patterns of a selected number of catalyst classes is accompanied with a density functional theory investigation of fragmentation intermediates in order to assess the viability of a selected fragmentation mechanism. 相似文献
74.
The TiNiSi type intermetallic compounds RERhZn (RE = Y, Sm, Gd–Lu) were synthesized by induction melting of the elements in sealed tantalum ampoules. They were characterized by X-ray powder diffraction. Five structures were refined from single crystal X-ray diffractometer data: Pnma, Z = 4, a = 699.7(2), b = 405.6(2), c = 816.9(2) pm, wR2 = 0.038, 628 F2 values for SmRhZn, a = 696.1(2), b = 405.6(1), c = 811.9(3) pm, wR2 = 0.028, 886 F2 values for GdRhZn, a = 692.8(1), b = 403.0(1), c = 809.5(2) pm, wR2 = 0.039, 562 F2 values, for TbRhZn, a = 690.6(3), b = 401.50(9), c = 808.2(2) pm, wR2 = 0.036, 763 F2 values, for DyRhZn, and a = 688.6(5), b = 399.6(4), c = 808.3(7) pm, wR2 = 0.048, 546 F2 values for HoRhZn with 20 variables for each refinement. The rhodium atoms have coordination number 9 (5 RE + 4 Zn atoms) in the form of a tricapped trigonal prism. Together the rhodium and zinc atoms build up three-dimensional [RhZn] networks with short Rh–Zn (263–269 pm in GdRhZn) and Zn–Zn (296 pm in GdRhZn) distances. The gadolinium atoms bind to the [RhZn] network by Gd–Rh bonds (292–294 pm). Magnetic susceptibility measurements show Pauli paramagnetism for YRhZn and van Vleck paramagnetism for SmRhZn. The remaining RERhZn compounds are Curie–Weiss paramagnets which show magnetic ordering at low temperatures. 相似文献
75.
Ferry Heus Martin Giera Gerdien E. de Kloe Dick van Iperen Joost Buijs Tariq T. Nahar August B. Smit Henk Lingeman Iwan J. P. de Esch Wilfried M. A. Niessen Hubertus Irth Jeroen Kool 《Analytical and bioanalytical chemistry》2010,398(7-8):3023-3032
One way to profile complex mixtures for receptor affinity is to couple liquid chromatography (LC) on-line to biochemical detection (BCD). A drawback of this hyphenated screening approach is the relatively high consumption of sample, receptor protein and (fluorescently labeled) tracer ligand. Here, we worked toward minimization of sample and reagent consumption, by coupling nano-LC on-line to a light-emitting diode (LED) based capillary confocal fluorescence detection system capable of on-line BCD with low-flow rates. In this fluorescence detection system, a capillary with an extended light path (bubble cell) was used as a detection cell in order to enhance sensitivity. The technology was applied to a fluorescent enhancement bioassay for the acetylcholine binding protein, a structural analog of the extracellular ligand-binding domain of neuronal nicotinic acetylcholine receptors. In the miniaturized setup, the sensitive and low void volume LED-induced confocal fluorescence detection system operated in flow injection analysis mode allowing the measurement of IC50 values, which were comparable with those measured by a conventional plate reader bioassay. The current setup uses 50 nL as injection volume with a carrier flow rate of 400 nL/min. Finally, coupling of the detection system to gradient reversed-phase nano-LC allowed analysis of mixtures in order to identify the bioactive compounds present by injecting 10 nL of each mixture. 相似文献
76.
Friedrich Schoder Ulrike Plaia Robert Metzner Wilfried Sperber Wolfgang Beck Wolf Peter Fehlhammer Prof. Dr. 《无机化学与普通化学杂志》2010,636(5):700-709
The reactions of [Re(CO)6]+, [FeCp(CO)2CS]+ and [FeCp(CNPh)3]+ with the metallo nitrile ylides [M–{C+=N–C–(H)CO2Et}(CO)5]– (M = Cr, W) and the chromio nitrile imine [Cr–{C+=N–N–H}(CO)5]– (generated by mono‐α‐deprotonation of the parent isocyanide complexes) to give neutral 5‐metallated 1,3‐oxazolin‐ ( 1 ), 1,3‐thiazolin‐ ( 2 ), imidazolin‐ ( 3 , 4 ), 1,3,4‐oxdiazolin‐ ( 5 ), 1,3,4‐thiadiazolin‐ ( 6 ) and 1,3,4‐triazolin‐2‐ylidene ( 8 ) chromium and tungsten complexes represent the first all‐organometallic versions of Huisgen’s 1,3‐dipolar cycloadditions. The formation of 6 and 8 is accompanied by partial decomposition to (OC)5Cr–C≡N–FeCpL2 {L = CO ( 7 ), CNPh ( 9 )}. The structures of 4a and 5 have been characterized by X‐ray diffraction. 相似文献
77.
Martin Giera Jon S. B. de Vlieger Henk Lingeman Hubertus Irth Wilfried M. A. Niessen 《Rapid communications in mass spectrometry : RCM》2010,24(10):1439-1446
Structural elucidation of six regioisomers of mono‐N‐octyl derivatized neomycin is achieved using MSn (up to n = 4) on an ion trap time‐of‐flight (IT‐TOF) instrument equipped with electrospray ionization. The mixture of six derivatized neomycin analogues was generated by reductive amination in a shotgun synthetic approach. In parallel to the liquid chromatography/mass spectrometry (LC/MS) detection, the antibacterial activity of the neomycin regioisomers was tested by post‐column addition of buffer and bacterial inocula, subsequent microfractionation of the resulting mixture, incubation, and finally a chemiluminescence‐based bioactivity measurement based on the production of bacterial ATP. The MS‐based high‐resolution screening approach described can be applied in medicinal chemistry to help in designing and producing new antibiotic substances, which is particularly challenging due to the high functionality of most antibiotic substances, therefore requiring advanced (hyphenated) separation and detection techniques for compound mixtures. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
78.
Heptakis(2,6‐di‐O‐methyl‐3‐O‐pentyl)‐β‐cyclodextrin was monofunctionalized by the regioselective introduction of exactly one ω‐epoxyoctyl group at the primary site of the cyclodextrin. The site‐specifically substituted cyclodextrin was immobilized to commercially available aminopropyl silica by nucleophilic opening of the epoxy function of the spacer substituent resulting in a lipophilic chiral stationary phase with broad applicability for enantiomer separations in capillary‐HPLC under reversed‐phase conditions. 相似文献
79.
80.
Gerda Rogl Viktor Soprunyuk Wilfried Schranz Michael J. Zehetbauer Jiri Bursik Herbert Müller Ernst Bauer Peter F. Rogl 《无机化学与普通化学杂志》2020,646(14):1267-1272
Thermoelectric materials with a high figure of merit, ZT, are the essential basis to build thermoelectric generators, which can directly convert heat into electricity. Severe plastic deformation (SPD) via high-pressure torsion (HPT) was successfully applied to enhance ZT of ball-milled and hot-pressed skutterudites as well as to produce bulk nanostructured skutterudites directly from powders. SPD introduces many defects into the sample and in parallel the crystallite size is significantly reduced. During measurement-induced heating these defects anneal partially out, and the grains grow. In this work for the first time systematically the changes of the temperature-dependent electrical resistivity and of thermal expansion were compared. It could be shown that for p- and n-type skutterudites, being hot-pressed and HPT-processed as well as directly HPT-processed from compacted powder, these changes occur more or less simultaneously within the same temperature ranges. This evaluation gives a much deeper insight into the thermoelectric behavior of HPT samples under the influence of changing temperature. 相似文献