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1.
Dynamical Behaviour of Linear Molecular Anions in the Hydrogensulfides of Sodium, Potassium and Rubidium: Differential Scanning Calorimetry, X-ray and Neutron Diffraction Hydrogensulfides of the alkali metals M ? Na, K, Rb were prepared in autoclaves by the reaction of the corresponding metals with H2S and D2S, respectively, in the temperature range from 50°C to 150°C. Differential scanning calorimetry, X-ray and neutron diffraction methods reveal that both, the HS?-and DS?-compounds occur in three crystalline modifications with HT ? high-, MT ? medium- and LT ? low-temperature form: The temperatures and enthalpies for the changes of modifications of the H- and D-compounds are given and the atomic arrangements revealed mainly by neutron diffraction data are discussed, in relation to, for example, size of cations. 相似文献
2.
3.
Nowaczyk S Alayrac C Metzner P Averbuch-Pouchot MT 《The Journal of organic chemistry》2002,67(19):6852-6855
The alkylation of the lithium enolate of enantiopure alpha-cyclohexylsulfinyl thioacetamide 1 with allyl bromides 5 possessing an electron-withdrawing group at the vinylic position does not occur at the sulfur center - as expected in the sulfur series - but at the carbon center through conjugate addition followed by bromide elimination. The modest to excellent 1,2-asymmetric induction achieved by the alkylsulfinyl group (dr up to 100:0) is explained by an electronic model. 相似文献
4.
A fast Blümlein circuit with a water strip line having an impedance of Z=0.078 is used to excite a TE high power nitrogen laser at =337 nm. A pseudospark switch works as a high power switch. The laser operates without any preionization and delivers an energy of 15 mJ per pulse (7.5 ns FWHM) at 10 kPa nitrogen pressure. The shot to shot reproducibility is better than 5%. 相似文献
5.
Patrick Metzner Jean-François Brière Hiroya Takada 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3-4):965-968
Abstract The reaction of novel chiral selenonium and telluronium ylides was investigated with aldehydes and compared to the sulfur analogues. (2R,5R)-2,5-Dimethylselenolane was prepared and reacted as a catalyst for the benzylidenation of aldehydes. Disubstituted epoxides were readily prepared with a (surprising) absence of diastereoselectivity, and with enantiomeric excesses higher than 90%. The reaction of a tellurium analogue, (2S,5S)-2,5-diethyltellurolane, afforded the oxirane in very moderate yield and e.e.'s in the range of 62–82%. Though this was less productive, it is the first report of a chiral telluronium ylide leading to an asymmetric epoxidation of aldehydes. 相似文献
6.
Virginie Blot Jean-François Brièr Marion Davoust Stéphanie Minière Vincent Reboul Patrick Metzner 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5-6):1171-1182
Abstract Our work on the thio-Claisen rearrangement mediated by an adjacent sulfinyl group is reviewed. The substrates could easily be prepared on a large scale from diacetone-D-glucose. The rearrangement was effected with a diastereoselectivity of 95:5, in favor of the (S,S) or the (R,R) isomer. An approach to natural bis(lactones) was investigated, using a halolactonization reaction and a second [3,3] sigmatropic shift, again mediated by the sulfinyl group. The second part deals with the catalytic enantioselective benzylidenation of aldehydes, mediated by chiral sulfur ylides. We have introduced simple C 2 symmetric thiolanes for that purpose. The procedure is very practical and enantiomeric excesses up to 96% have been reported for the model of stilbene oxide. A series of ferrocenyl sulfides with planar chirality has also been investigated, leading to unexpected diastereoselectivities and enantiomeric excesses up to 94%. 相似文献
7.
The 1,3-asymmetric iodolactonization reaction of enantiopure alpha-sulfurated gamma-unsaturated amides has been investigated. With sulfinyl and sulfonyl groups, a poorly stereoselective reaction was observed, whereas with a sulfanyl moiety, the diastereoselectivity can be high as 96:4. The role of the oxygen atom on the sulfur moiety is discussed. 相似文献
8.
Walter Metzner 《Foundations of Physics》2000,30(12):2101-2112
It is shown that the existence of d-wave superconductivity in the two-dimensional Hubbard model close to half-filling can be inferred from a renormalization group analysis at one-loop level. 相似文献
9.
Friedrich Schoder Ulrike Plaia Robert Metzner Wilfried Sperber Wolfgang Beck Wolf Peter Fehlhammer Prof. Dr. 《无机化学与普通化学杂志》2010,636(5):700-709
The reactions of [Re(CO)6]+, [FeCp(CO)2CS]+ and [FeCp(CNPh)3]+ with the metallo nitrile ylides [M–{C+=N–C–(H)CO2Et}(CO)5]– (M = Cr, W) and the chromio nitrile imine [Cr–{C+=N–N–H}(CO)5]– (generated by mono‐α‐deprotonation of the parent isocyanide complexes) to give neutral 5‐metallated 1,3‐oxazolin‐ ( 1 ), 1,3‐thiazolin‐ ( 2 ), imidazolin‐ ( 3 , 4 ), 1,3,4‐oxdiazolin‐ ( 5 ), 1,3,4‐thiadiazolin‐ ( 6 ) and 1,3,4‐triazolin‐2‐ylidene ( 8 ) chromium and tungsten complexes represent the first all‐organometallic versions of Huisgen’s 1,3‐dipolar cycloadditions. The formation of 6 and 8 is accompanied by partial decomposition to (OC)5Cr–C≡N–FeCpL2 {L = CO ( 7 ), CNPh ( 9 )}. The structures of 4a and 5 have been characterized by X‐ray diffraction. 相似文献
10.
Using metallic indium doped with radioactive111In as one of the starting materials samples of stoichiometric CuInS2, CuInS2 with excess of indium and sulphur, and stoichiometric CuIn5S8 were prepared. Perturbed angular correlations of γ rays emitted by111Cd are utilized to analyse the produced crystalline phases. 相似文献