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991.
992.
Experiments on the reaction:3He+3He→4He+2He using a single four detector telescope have shown evidence for the production of deuteron pulses, consistent with the2He→2H+e++v fusion reaction in the final state. New measurements on the same reaction using improved techniques viz.A) a windowless3He gas target andB) α- d correlation detection with 5 ns resolving time and antipileup circuitry have been performed. Calibrations were obtained from the7Li+3He→2H+4He+4He reaction spectra. The correlation angles were 30° and 97° for the alphas and deuterons respectively. Deuteron pulses have been observed, correlated with alpha particles. A cross section of (1.7 ±0.5)nbsr?1MeV?1 was obtained consistent with previous measurements using a single telescope.  相似文献   
993.
An innovative and facile synthesis of the title compound has been developed starting from (R)-cyclohexylidene glyceraldehyde. The key step in the synthesis is a chiral template-driven Grignard addition with absolute diastereocontrol. The other attractive features are the operational simplicity and the use of inexpensive compounds/reagents.  相似文献   
994.
Sen N  Roy NK  Das AK 《Talanta》1989,36(6):697-699
Separation by solvent extraction followed by X-ray fluorescence spectrometry has been used for determination of molybdenum and tungsten in rocks and minerals. Samples are decomposed either by heating with a mixture of hydrofluoric acid and perchloric acid or by fusion with potassium pyrosulphate, followed by extraction of molybdenum and tungsten with N-benzoylphenylhydroxylamine in toluene from 4-5M sulphuric acid medium. The extract is collected on a mass of cellulose powder, which is dried in vacuum, mixed thoroughly and pressed into a disc for XRF measurements. The method is free from all matrix effects and needs no mathematical corrections for interelement effects. The method is suitable for determination of molybdenum and tungsten in geological materials down to ppm levels, with reasonable precision and accuracy.  相似文献   
995.
The first example of a pair of interconvertible diastereomeric epimers 2α/2β-hydroxy-2-p-hydroxybenzyl-3(2H)-benzofuranone-7-C-β-d-glucopyranoside isolated from the heartwood of Pterocarpus marsupium is reported. The predominance of 1a over 1b was supported by dynamic exchange rates and activation parameters obtained from NMR studies. The mechanism of this unique phenomenon is thought to be operative by the formation of diketone as suggested by deuterium exchange.  相似文献   
996.
The interaction of a cyanonitrosyl–manganate complex with DNA has been studied by u.v.–vis spectroscopy, circular dichroism, fluorescence and gel electrophoresis techniques. As the DNA 260 nm band remained insensitive to interaction, the interaction ratio was determined by monitoring the CN→ Mn LMCT band observed at 222 nm, and the interaction ratio was found to be in the complex (D): DNA (P)=1:0.30 from the spectrophotometric titration. The above-mentioned physical measurements indicate that the binding mode is not intercalative and the cyanonitrosyl system is a groove binder.  相似文献   
997.
The superheated emulsion, a radiation detector consisting of superheated droplets dispersed in a gel or a solid matrix, has been in use for some time now. It was initially designed to detect neutrons but also has been modified to detect energetic photons and heavy ions. It has been primarily used as a neutron dosimeter, but has also been used to obtain the energy spectrum for neutrons from Am–Be. The general features of the superheated emulsion detector along with newer analytic methods to obtain more precise results using it as an active device will be presented.  相似文献   
998.
2,2,2-Trifluorodiazoethane reacts with trifluoroacetonitrile in the dark at room temperature to give a 2-(2,2,2-trifluoroethyl)-4, 5-bis(trifluoromethyl)triazole, the 1,2,3-triazole structure being preferred to the 1,2,4-isomer on the basis of the 19F n.m.r. spectrum. The diazoethane reacts more slowly with trichloroacetonitrile, again forming the N-alkylated triazole even in the presence of an excess of the nitrile. No identifiable adduct resulted with acetonitrile. Hexafluoroisopropyl-ideneimine is first N-alkylated and then undergoes addition to form 1-(2,2,2-trifluoro-1-trifluoromethyl)ethyl-4,5-bis(trifluoromethyl)-?-1,2,3-triazoline, but N-methylhexafluoroisopropylideneimine failed to react. Trifluoroacetaldehyde and trichloroacetaldehyde give mixtures of the ketone (formed by insertion of the CF3CH group into the aldehyde CH bond) and the cis- and trans-oxirans, apparently via a β-hydroxydiazoalkane.  相似文献   
999.
The possible topological structures of elementary particles have been investigated to explore the possibility of the existence of magnetic monopoles. It is pointed out that when an elementary charged particle is depicted as an extended body such that the orientation of the internal space (internal helicity) defines the fermion number, the global conservation of this does not allow the existence of a magnetic monopole. Again it is argued that when anisotropy is introduced in the microlocal space-time depicting the internal space of hadrons, this gives rise to the internal symmetry algebra and no non-Abelian gauge fields and Higgs scalars are necessary to have a grand unified scheme of interactions. This avoids theSU 2 and GUT monopoles. Besides, in this formalism, baryon number corresponds to the orientation or internal helicity of the composite system and the global conservation of this quantum number is found to be a consequence of Lorentz invariance. This forbids the existence of any sort of cosmological monopole in this Lorentz invariant Universe.  相似文献   
1000.
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