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1.
2.
Eckhard Herrmann Moein Nouaman Zdirad
k Gisbert Großmann Gisela Ohms 《无机化学与普通化学杂志》1994,620(11):1879-1888
Tetraarylesters of μ-Imido-Diphosphoric Acid and its Thio Derivatives — Structure Investigations New O,O′,O″,O?-tetratolyl- and ditolyl-diphenylesters of the μ-imido-diphosphoric acid and its mono and dithio derivatives were synthesized, compared with the corresponding tetraphenylesters and investigated by 1H, 13C, and 31P NMR spectroscopy and X-ray crystal structure analysis. Structures of the O,O′,O″,O?-tetrakis-(2-methyl-phenyl)-μ-imidodiphosphate, 1b , as well as of the corresponding ortho-, meta- and para-tolylesters of the μ-imido-monothiodiphosphoric acid ( 2a , 2b , 2c ) were determined. All the compounds form dimers via N? H…?O hydrogen bonds in the crystal as well as in nonpolar solvents. The distances around the phosphorus atoms rise with decreasing electronegativity of the phosphorus substituents. Signs of the 2JP? N? P coupling constants were determined by 13C{1H, 31P} triple resonance experiments for some compounds. These constants become more negative owing to substitution of a phosphoryl by a thiophosphoryl group. 相似文献
3.
Hegedus LS Geisler L Riches AG Salman SS Umbricht G 《The Journal of organic chemistry》2002,67(22):7649-7655
Butenolides 5a and 13 were used as optically active templates in the de novo synthesis of 4'-disubstituted nucleoside analogues. The butenolides were reduced and acylated in situ to give acetates 10 and 14. Vorbrüggen coupling gave the protected nucleoside analogues 11 and 15. Reduction of 11 gave 4'-ethoxy-2',3'-dideoxythymidine (6) and deprotection of 15 gave 4'-ethoxy-2',3'-dideoxydidehydrothymidine (7). The cis-dihydroxylation of a variety of butenolides occurred with the major product formed from oxidation of the beta-face. 相似文献
4.
Gisela Bodrogai 《Mikrochimica acta》1979,71(1-2):47-51
Zusammenfassung Verschiedene schwefelhaltige Verbindungen ergeben zu hohe Kohlenstoffwerte. Dieser Fehler kann behoben werden, indem die Einwaage im Verbrennungsschiffchen mit vorbehandeltem Cerdioxid abgedeckt oder vermischt wird.
CH determination in containing compounds sulfur
Summary Various sulfur-containing compounds yield carbon values which are too high. This error can be eliminated by covering or mixing the aliquot in combustion boats with pretreated cerium dioxide.相似文献
5.
To avoid changes in the original As species distribution in natural water after sampling, a method of immediate separation
of As(V) by anion exchange at the sampling site was developed. The procedure consists of two steps. The total concentration
of arsenic is determined in one part of the water sample acidified on site. Another part of the water samples is pressed through
a column filled with an anion exchanger. The As(III) species that is not redox-stable remains in the effluent of the sorbents
column and can be analyzed with conventional methods after stabilization by addition of conc. HNO3. As(V) is sorbed by the exchanger material. The As(V) concentration can be calculated as the difference between Assol and As(III), neglecting very low contents of methylated species.
Oxidation of Fe(II) by air followed by co-precipitation of arsenic with iron hydroxide was applied in field experiments to
minimize the As concentration in seepage and mining water. 相似文献
6.
The synthesis of a series of enantiomerically pure, C2-symmetric 4,4′,5,5′-tetrahydro-2,2′-methylenebis[oxazoles] and 4,4′,5,5′-tetrahydro-2,2′-bi(oxazoles) is reported. Copper complexes with anionic tetrahydromethylenebis[oxazole] ligands are efficient catalysts for the enantioselective cyclopropane formation from olefins and diazo compounds (up to 96% ee in the reaction of styrene with menthyl diazoacetate). Tetrahydrobi(oxazole)iridium(I) complexes were found to catalyze transfer hydrogenations of aryl alkyl ketones with i-PrOH (up to 91% ee). Tetrahydrobi(oxazole)palladium complexes can be used as enantioselective catalysts for allylic nucleophilic substitution (up to 77% ee in the reaction of PhCH?CHCH(OAc)Ph with NaHC(COOMe)2). 相似文献
7.
Reyhaneh Armin Sebastian Zühlke Gisela Grunewaldt-Stcker Felix Mahnkopp-Dirks Souvik Kusari 《Molecules (Basel, Switzerland)》2021,26(12)
Apple Replant Disease (ARD) is a significant problem in apple orchards that causes root tissue damage, stunted plant growth, and decline in fruit quality, size, and overall yield. Dysbiosis of apple root-associated microbiome and selective richness of Streptomyces species in the rhizosphere typically concurs root impairment associated with ARD. However, possible roles of Streptomyces secondary metabolites within these observations remain unstudied. Therefore, we employed the One Strain Many Compounds (OSMAC) approach coupled to high-performance liquid chromatography-high-resolution tandem mass spectrometry (HPLC-HRMSn) to evaluate the chemical ecology of an apple root-associated Streptomyces ciscaucasicus strain GS2, temporally over 14 days. The chemical OSMAC approach comprised cultivation media alterations using six different media compositions, which led to the biosynthesis of the iron-chelated siderophores, ferrioxamines. The biological OSMAC approach was concomitantly applied by dual-culture cultivation for microorganismal interactions with an endophytic Streptomyces pulveraceus strain ES16 and the pathogen Cylindrocarpon olidum. This led to the modulation of ferrioxamines produced and further triggered biosynthesis of the unchelated siderophores, desferrioxamines. The structures of the compounds were elucidated using HRMSn and by comparison with the literature. We evaluated the dynamics of siderophore production under the combined influence of chemical and biological OSMAC triggers, temporally over 3, 7, and 14 days, to discern the strain’s siderophore-mediated chemical ecology. We discuss our results based on the plausible chemical implications of S. ciscaucasicus strain GS2 in the rhizosphere. 相似文献
8.
M. Zürcher und Gisela Hoepe 《Fresenius' Journal of Analytical Chemistry》1940,119(3-4):134-136
Ohne Zusammenfassung 相似文献
9.
Manfred Rätzsch Gottfried Haudel Gisela Pompe Evelyn Meyer 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(13-14):1631-1655
10.
Franz Dalitz Lennart Kreckel Michael Maiwald Gisela Guthausen 《Applied magnetic resonance》2014,45(5):411-425
Medium-resolution nuclear magnetic resonance spectroscopy is a promising tool for the monitoring of liquid reactions. For process analytical applications, the requirements of robustness and insensitivity of the spectrometer in relation to high temperatures and pressures are challenging. Within this study, a flow probe using a glass dewar is presented. Temperatures of flowing samples up to 130 °C and pressures up to 40 bar were successfully applied, and the corresponding temperature loss of the flowing sample at 2 ml min?1 was <2.4 °C at 130 °C. Furthermore, if the process requires a measurement in a non-equilibrium state of magnetization, a comprehensive data treatment is given. For this purpose, the influences of the flow and T 1 of the substances under investigation are studied in detail on the example of a homogeneously catalyzed esterification. In addition, data analysis schemes were designed such that the experiments directly revealed mole fractions from the spectra. Limited spectral resolutions and low signal-to-noise ratio still did not obstruct quantitative interpretation of the experiments. 相似文献