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91.
Uwe Klingebiel Detlev Enterling Lutz Skoda Anton Meller 《Journal of organometallic chemistry》1977,135(2):167-172
Fluorosilyl substituted cyclosilazanes are formed by treating lithium salts of hexamethylcyclotri- and octa-methylcyclotetrasilazanes with silicon tetrafluoride and organo-substituted silicon fluorides. Disubstituted compounds are obtained by the reaction of dilithium hexamethylcyclotrisilazane with silicon fluorides or by the reaction of lithium hexamethylcyclotrisilazane with silicon fluorides at higher temperature. Cyclosilazanes with bulky ligands react with butyllithium with elimination of butane as a first step and then react further with a silicon fluoride compound, with LiF-elimination, to give a mixed substituted cyclosilazane. Ring coupling through a silicon bridge is achieved by the reaction of a fluorosilyl-substituted cyclotrisilazane with lithium hexamethylcyclotrisilazane. The mass,1H and19F NMR spectra of the compounds are reported. 相似文献
92.
Alkoxylierung von bis(trimethylsilyl)-aminofluorsilanen,sowie siloxanbildung unter äthereliminierung
Uwe Klingebiel Dietrich Fischer Anton Meller 《Journal of organometallic chemistry》1975,85(2):141-147
The reaction of bis(trimethylsilyl)aminofluorsilanes, (Me3Si)2NSiF2R (R = CH3 or F), with sodium alcoholates or sodium phenylate yields under elimination of NaF alkoxy- and aryloxy-aminofluorosilanes of the composition (Me3Si)2NSiF(R)OR′(R′ = CH3, C2H5, C3H7, C6H5). A disiloxane is formed by thermal elimination of diethyl ether from bis(trimethylsilyl)aminomethylfluoroethoxysilane. The IR, mass, 1H and 19F NMR spectra of the above-mentioned compounds are reported. ab]Die Reaktion von Bis(trimethylsilyl)-aminofluorsilanen des Typs (Me3Si)2NSiF2R (R = F, CH3) mit Natriumalkoholaten und Natriumphenolat führt unter NaF-Abspaltung zu Alkyl- und Aryloxyaminofluorsilanen der Zusammensetzung: (Me3Si)2NSiF(R)OR′ (R′ = CH3, C2H7, C6H5, C6H5). Ein Disiloxan könnte durch die thermische Eliminierung von Diäthyläther aus Bis(trimethylsilyl)aminomethyl-fluor-äthoxy-silylarnin erhalten werden.Die IR-, Massen-, 1H- und 19F-NMR-Spektren der dargestellten Verbindungen werden mitgeteilt. 相似文献
93.
J. Maštovský J. Blaha L. Rothhardt G. Jahn H. Kneipp 《Czechoslovak Journal of Physics》1976,26(8):860-862
The limitation of the applicability of plasma eaters in mixtures of argon with molecular components is shown. We were able to measuren
e
andT
e
in argon-hydrogen mixture behind the reflected shock wave and find a strong reduction of both parameters caused by the molecular species. Similarly, the delay of the onset of ionization in argon-hydrogen and argon-nitrogen mixtures is substantially reduced. On the other hand, the molecular component reduces the velocity of thermodynamic equilibration, as has been shown by means of time resolved optical interferometry. 相似文献
94.
F. zu Bentheim P. David J. Debrus F. Hinterberger R. Jahn F. Lübke H. Mommsen R. Schoenmackers B. Schüller 《Zeitschrift für Physik A Hadrons and Nuclei》1976,40(3):163-168
Experimental data of the elastic scattering of-particles on10B forE
= 30–50.6 MeV are presented. They are analysed together with the data of a previous measurement forE
= 5–30 MeV in the frame of the optical model including spin-orbit coupling. The interaction radii of the-10B-systems are determined with the Inopin-Ericson model forE
= 5–50 MeV. The mean free path of-particles in10B is calculated. 相似文献
95.
Marine Rémy Dr. Iwona Nierengarten Boram Park Dr. Michel Holler Dr. Uwe Hahn Dr. Jean-François Nierengarten 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(33):8492-8499
Stable pillar[5]arene-containing [2]rotaxane building blocks with pentafluorophenyl ester stoppers have been efficiently prepared on a multi-gram scale. Reaction of these building blocks with various nucleophiles gave access to a wide range of [2]rotaxanes with amide, ester or thioester stoppers in good to excellent yields. The rotaxane structure is fully preserved during these chemical transformations. Actually, the addition-elimination mechanism at work during these transformations totally prevents the unthreading of the axle moiety of the mechanically interlocked system. The stopper exchange reactions were optimized both in solution and under mechanochemical solvent-free conditions. While amide formation is more efficient in solution, the solvent-free conditions are more powerful for the transesterification reactions. Starting from a fullerene-functionalized pillar[5]arene derivative, this new strategy gave easy access to a photoactive [2]rotaxane incorporating a C60 moiety and two Bodipy stoppers. Despite the absence of covalent connectivity between the Bodipy and the fullerene moieties in this photoactive molecular device, efficient through-space excited state interactions have been evidenced in this rotaxane. 相似文献
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100.
Andreas Uwe Meyer Karolína Straková Dr. Tomáš Slanina Prof. Dr. Burkhard König 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(25):8694-8699
Alkyl‐ and aryl vinyl sulfones were obtained by eosin Y (EY)‐mediated visible‐light photooxidation of sulfinate salts and the reaction of the resulting S‐centered radicals with alkenes. Optimized reaction conditions, the sulfinate and alkene scope, and X‐ray structural analyses of several reaction products are provided. A detailed spectroscopic study explains the reaction mechanism, which proceeds through the EY radical cation as key intermediate oxidizing the sulfinate salts. 相似文献