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Hans-Georg Rück 《Archiv der Mathematik》1984,43(2):145-147
Ohne Zusammenfassung 相似文献
75.
Braun T Izundu J Steffen A Neumann B Stammler HG 《Dalton transactions (Cambridge, England : 2003)》2006,(43):5118-5123
The chloro and azido complexes trans-[PdCl(4-C5NF4)(PiPr3)2] (3) and trans-[Pd(N3)(4-C5NF4)(PiPr3)2] (4) can be prepared by reaction of [PdF(4-C5NF4)(PiPr3)2] (2) with Et3SiCl or MeSiN3, respectively. In contrast, reactions of 2 with Ph3SiH or Me2FSiSiFMe2 give the products of reductive elimination 2,3,5,6-tetrafluoropyridine (5) or 4-(fluorodimethylsilyl)tetrafluoropyridine (6) as well as [Pd(PiPr3)2] (1). In a catalytic experiment, pentafluoropyridine can be converted with Ph3SiH into 5 in 62% yield, when 10% of 2 is employed as catalyst. Treatment of trans-[PdF(4-C5NF4)(PiPr3)2] (2) with Bu3SnCH=CH2 in THF at 50 degrees C results in the formation of [Pd(PiPr3)2] (1) and 4-vinyltetrafluoropyridine (7). Complex 2 is also active as a catalyst towards a Stille cross-coupling reaction of pentafluoropyridine with Bu3SnCH=CH2 to give 4-vinyltetrafluoropyridine (7) with a TON of 6. The molecular structure of the complex 3 has been determined by X-ray crystallography. 相似文献
76.
Theo Scholtes Stefan Woetzel Rob IJsselsteijn Volkmar Schultze Hans-Georg Meyer 《Applied physics. B, Lasers and optics》2014,117(1):211-218
The intrinsic relaxation rates of the vector magnetization of cesium vapor enclosed in microfabricated atomic magnetometer cells are investigated. Two methods—the optically detected magnetic resonance and the ground-state Hanle effect—are used to carry out automated measurements in dependence on cell temperature and nitrogen buffer gas pressure. The experimental results are compared with expected contributions of the different relaxation processes and in this way allow the discrimination between them to help further optimization of cell design. The methods are compared in terms of basic features, data quality, and practical applicability. 相似文献
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Dr. Lucas Wickemeyer Prof. Dr. Israel Fernández Beate Neumann Dr. Hans-Georg Stammler Prof. Dr. Norbert W. Mitzel 《Angewandte Chemie (International ed. in English)》2023,62(11):e202216943
The reaction of the oxygen-bridged frustrated Lewis pairs (FLPs) tBu2P−O−Si(C2F5)3 ( 1 ) and tBu2P−O−AlBis2 ( 2 ) with azobenzene, promoted by UV irradiation, led to a selective complexation of the cis-isomer. The addition product of 2 is stable, while the adduct of 1 isomerizes in solution in an ortho-benzidine-like [3,3]-rearrangement by cleavage of the N−N bond, saturation of the nitrogen atoms with hydrogen atoms and formation of a new bond between two phenyl ortho-carbon atoms. Similar rearrangements take place with different para-substituted azobenzenes (R=Me, OMe, Cl) and di(2-naphthyl)diazene, while ortho-methylated azo compounds do not form adducts with 1 . All adducts were characterized by multinuclear NMR spectroscopy and elemental analyses and the mechanism of the rearrangement was explored by quantum-chemical calculations. 相似文献
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Schmarr HG Potouridis T Ganss S Sang W Köpp B Bokuz U Fischer U 《Analytica chimica acta》2008,617(1-2):119-131
An improved method for the analysis of carbonyls is described utilizing a headspace solid-phase microextraction (HS-SPME) step and on-fiber derivatization with O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine (PFBHA) hydrochloride. Thermal desorption of the oxime derivatives formed on the fiber is followed by gas chromatographic separation coupled to an ion trap tandem mass spectrometer (GC-ITMS). Selecting specific fragment ions within the electron ionization (EI(+)) mass spectra of these oxime derivatives as precursor ions for MS-MS fragmentation provides a suitable method for the target analysis of individual carbonyl classes, such as alkanals, (E)-2-alkenals, (E,E)-2,4-alkadienals, and others. Retention indices on polar as well as on apolar stationary phases along with EI(+) mass spectra patterns are presented for a large set of oxime derivatives, giving valuable information needed for unambiguous assignment of substances in complex sample matrices. The fast sample preparation and derivatization step via HS-SPME can be automated and is applicable to a variety of biological samples and foodstuffs, allowing rapid and sensitive screening analyses of important aldehydic biomarkers and aroma active compounds. 相似文献