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Mandy Eibisch Sebastian Zellmer Rolf Gebhardt Rosmarie Süß Beate Fuchs Jürgen Schiller 《Rapid communications in mass spectrometry : RCM》2011,25(18):2619-2626
The liver is an important organ that is particularly involved in the lipid metabolism of the organism. Thus, high interest is nowadays focused on the lipid composition of the liver and particularly the liver parenchymal cells, the hepatocytes. Hepatocytes contain common phospholipids (PL) such as phosphatidylcholines, ‐ethanolamines and ‐inositols, for instance, that can be easily analyzed by matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS) even without previous separation of the PL mixture. However, in addition to common PL, hepatocytes possess also significant amounts of cardiolipin (CLP). The MS analysis of this PL is quite challenging because it (a) has a higher mass than common lipids and (b) possesses a higher negative charge. We will show here that caution is required if CLP is analyzed directly from the total lipid extract because PC dimers may be interpreted as cardiolipins if the positive ion MALDI mass spectra are analyzed. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
55.
Susan Torabi Lukas Hammerschmidt Elena Voloshina Beate Paulus 《International journal of quantum chemistry》2014,114(14):943-951
The performance of wavefunction‐based correlation methods in theoretical solid‐state chemistry depends on reliable Hartree–Fock (HF) results for infinitly extended systems. Therefore, we optimized basis sets of valence‐triple‐ζ quality based on HF calculations for the periodic system of group‐12‐metal difluorides. Scalar‐relativistic effects were included in the case of the metal‐ions by applying small‐core pseudopotentials. To assess the quality of the proposed basis sets, the structural parameters, bulk moduli as well as cohesive and lattice energies of the systems were evaluated at the HF and the density functional theory levels. In addition to these two mean‐field approaches and to assess further employment of our basis sets to wavefunction‐based correlation methods we performed periodic local MP2 computations. Finally, the possibilities of pressure induced structural phase transitions occurring in the ZnF2, CdF2, and HgF2 were investigated. © 2014 Wiley Periodicals, Inc. 相似文献
56.
Lange H Maultzsch J Meng W Mollenhauer D Paulus B Peica N Schlecht S Thomsen C 《Langmuir : the ACS journal of surfaces and colloids》2011,27(11):7258-7264
We demonstrate a phase transfer method to create stable colloidal solutions of Au nanoparticles with 4-methoxypyridine ligands. We then investigate the adsorption behavior of 4-methoxypyridine onto gold surfaces by Raman spectroscopy, DFT calculations, and (1)H NMR. In contrast to unsubstituted pyridine and the frequently used (N,N-dimethylamino)pyridine (DMAP), a flat adsorption of 4-methoxypyridine on gold was found. 相似文献
57.
We describe the catalytic activity of the first chimeric ligase containing a foldameric sequence of β- and γ-amino acids. The chimeric backbone provides for the spatial arrangement of all functional groups involved in the formation of the catalytic site to allow efficient catalysis to take place. Our finding indicates significant progress in the field of functionally active artificial motifs. 相似文献
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Frank Strübe Jochen Mattay Beate Neumann Hans‐Georg Stammler 《Acta Crystallographica. Section C, Structural Chemistry》2011,67(1):o33-o36
Fulgides are a representative class of photochromic organic molecules which exhibit several interesting properties for diverse applications in fields such as data storage or high‐resolution spectroscopy. The crystal structures of three furyl fulgides with different steric constraints were determined and for two of the compounds both the E and Z isomer structures were defined. The compounds are 3‐[(E)‐1,3‐dimethyl‐4,5,6,7‐tetrahydro‐2‐benzofuran‐4‐ylidene]‐4‐isopropylidenetetrahydrofuran‐2,5‐dione, C17H18O4, (I‐E), 3‐[(E)‐1,3‐dimethyl‐5,6,7,8‐tetrahydro‐4H‐cyclohepta[c]furan‐4‐ylidene]‐4‐isopropylidenetetrahydrofuran‐2,5‐dione, C18H20O4, (II‐E), and the Z isomer, (II‐Z), and 3‐isopropylidene‐4‐[(E)‐1‐(5‐methoxy‐2‐methyl‐1‐benzofuran‐3‐yl)ethylidene]tetrahydrofuran‐2,5‐dione, C19H18O5, (III‐E), with two molecules in the asymmetric unit, and the Z isomer, (III‐Z). The structures of the E and Z isomers show only little differences in the bond lengths and angles inside the hexatriene unit. Because of the strained geometry there are deviations in the torsion angles. Furthermore, small differences in the distances between the bond‐forming C atoms in the electrocyclization process give no explanation for the unequal photochromic behaviour. 相似文献
60.
Johannes Wellmann Beate Hartmann Esther-Corinna Schwarze Silke Hillebrand Stephan I. Brueckner Jakob Ley Gerold Jerz Peter Winterhalter 《Molecules (Basel, Switzerland)》2022,27(11)
Previously, different Hydrangea macrophylla ssp. serrata cultivars were investigated by untargeted LC-MS analysis. From this, a list of tentatively identified and unknown compounds that differ significantly between these cultivars was obtained. Due to the lack of reference compounds, especially for dihydro-isocoumarins, we aimed to isolate and structurally characterise these compounds from the cultivar ‘Yae-no-amacha’ using NMR and LC-MS methods. For purification and isolation, counter-current chromatography was used in combination with reversed-phase preparative HPLC as an orthogonal and enhanced purification workflow. Thirteen dihydro-isocoumarins in combination with other metabolites could be isolated and structurally identified. Particularly interesting was the clarification of dihydrostilbenoid glycosides, which were described for the first time in H. macrophylla ssp. serrata. These results will help us in further studies on the biological interpretation of our data. 相似文献