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41.
F. Glaser 《Fresenius' Journal of Analytical Chemistry》1902,41(1):36-42
Ohne Zusammenfassung 相似文献
42.
43.
Sarkar U Glaser R Parsons ZD Barnes CL Gates KS 《Journal of chemical crystallography》2010,40(7):624-629
Abstract
1,2,4-Benzotriazine 1,4-di-N-oxides are potent antitumor drug candidates that undergo in vivo bioreduction leading to selective DNA damage in the low oxygen (hypoxic) cells found in tumors. Tirapazamine (TPZ) is the lead compound in this family. Here we report on the synthesis, crystal structure, and conformational analysis of a new analog, 3-cyclopropyl-1,2,4-benzotriazine 1,4-di-N-oxide (3). Compound 3 (C10H10N3O2) crystallized in the monoclinic space group C2/c. Unit cell parameters for 3: a = 16.6306 (12), b = 7.799 (5), c = 16.0113 (11) ?, α = 90, β = 119.0440 (10), γ = 90, and z = 8. 相似文献44.
de Fouquieres P Schirmer SG Glaser SJ Kuprov I 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2011,212(2):412-417
We report some improvements to the gradient ascent pulse engineering (GRAPE) algorithm for optimal control of spin ensembles and other quantum systems. These include more accurate gradients, convergence acceleration using the Broyden–Fletcher–Goldfarb–Shanno (BFGS) quasi-Newton algorithm as well as faster control derivative calculation algorithms. In all test systems, the wall clock time and the convergence rates show a considerable improvement over the approximate gradient ascent. 相似文献
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46.
Burkhard Luy Steffen J Glaser 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2000,142(2):280
Analytical polarization and coherence transfer functions are presented for a spin system consisting of three dipolar coupled homonuclear spins
under energy matched conditions. Based on these transfer functions, optimal durations of Hartmann–Hahn mixing periods can be determined for arbitrary dipolar coupling constants D12, D13, and D23. In addition, the dependence of the transfer efficiency on the relative size of the dipolar coupling constants is illustrated. 相似文献
47.
J. Clark H. K. Tompkins M. Höhnel C. Glaser O. Kassner S. Rideal H. J. Bult und Rossel 《Fresenius' Journal of Analytical Chemistry》1895,34(1):593-598
Ohne Zusammenfassung 相似文献
48.
49.
M Ehde L Pettersson J Glaser 《Acta chemica Scandinavica (Copenhagen, Denmark : 1989)》1991,45(10):998-1005
The two complexes formed in the aqueous vanadooxalate system, V(Ox)- and V(Ox)2(3-), have been characterized using 51V, 13C and 17O NMR. For the V(Ox)2(3-) complex, two peaks are observed in 13C NMR and four in 17O NMR. This leads to the conclusion that each oxalate ligand has two different distances to the VO2 group. This fact, together with the peak integrals and the chemical shifts, indicates strongly that the hexacoordinate complex [VO2(C2O4)2]3- found in single-crystal X-ray structure determinations persists in aqueous solution. The dependence of the 13C NMR linewidths upon temperature reveals two types of dynamic processes: (1) a rearrangement in which the two different V-Oox switch places and (2) an exchange of the oxalate ligands in the [VO2(C2O4)2]3- complex with free oxalate, probably through a dissociative process. Rate constants and activation parameters for the two dynamic processes involving [VO2(C2O4)2]3- have been calculated from the shape of the 13C NMR signals. For the V(Ox)- complex, only one relatively narrow peak is obtained in 13C NMR and three peaks in 17O. This fact, as well as the relative positions of these peaks, is in accordance with a pentacoordinate complex [VO2(C2O4)H2O]-, where the two V-O distances to the oxalate ligand are equal. We also show that, in the pH range 0.8-6.6, there is no protonation of the studied complexes, in agreement with previous potentiometric results. 相似文献
50.
Anuradha Ramoji Kerstin Galler Uwe Glaser Thomas Henkel Günter Mayer Jan Dellith Michael Bauer Jürgen Popp Ute Neugebauer 《Journal of Raman spectroscopy : JRS》2016,47(7):773-786
For Raman spectroscopic analyses of the cells and other biological samples, the choice of the right substrate material is very important to avoid loss of information in characteristic spectral features because of competing background signals. In the current study, Raman spectroscopy is used to characterize several potential Raman substrates. Raman vibrational bands of the substrate material are discussed. The surface topography is analyzed by atomic force microscopy, and the root mean square surface roughness values are reported. Biocompatibility of the substrates is tested with Hep G2 cells evaluating cellular morphology as well as live/dead staining. Calcium fluoride, silicon, fused silica, borofloat glass, and silicon nitride membranes support cell growth and adherence. Silicon, borofloat glass, and fused silica give rise to Raman signals in the region of interest. Calcium fluoride substrate (UV grade) is suitable for Raman spectroscopic investigation of living cells. Nickel foil is suitable substrate for Raman spectroscopic investigation but cellular adherence and viability depend on the quality of the foil. Silicon nitride membranes coated with nickel chrome is a suitable Raman substrate in closed microfluidic systems. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献