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The title 9-borabicyclo[3.3.1]nonane(9-BBN) ate complex (1) brings about selective removal of tertiary alkyl, benzyl and allyl halides to give the corresponding hydrocarbons in excellent yields without concomitant attack on secondary, primary and aryl derivatives. The reduction of cis- and trans - 4 - t - butyl - 1 - methylcyclohexyl chlorides (2) with 1 gives 4 - t - butyl - 1 - methylcyclohexanes (3) with partial inversion of configuration in cyclohexane, while that in benzene gives thermodynamically stable trans-3 predominantly. The reactions of 1,1 - dimethyl - 5 - hexenyl chloride (4) and 1,7,7 - trimethylbicyclo[2.2.1]hept - 2 - yl chloride (8) with 1 proceed with the rearrangements characteristic to a carbonium ion intermediate. The reduction of 1 - ethyl - 1 - methylpentyl chloride with 1 follows a second-order rate equation. 相似文献
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Hisanobu Ogoshi Kazurni Saita Ken-ichi Sakurai Takamichi Watanabe Hiroo Toi Yasuhiro Aoyama 《Tetrahedron letters》1986,27(52):6365-6368
Described is the preparation of chiral octaethylporphyrin derivatives having two 2-substituted naphthyl groups in a trans orientation at the 5- and 15-meso positions and formyl or hydroxymethyl or alkoxymethyl group derived therefrom at the 10-meso position. One of the derivatives has been successfully resolved into enantiomers by means of HPLC. 相似文献
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Ida K Funaba H Kado S Narihara K Tanaka K Takeiri Y Nakamura Y Ohyabu N Yamazaki K Yokoyama M Murakami S Ashikawa N deVries PC Emoto M Goto M Idei H Ikeda K Inagaki S Inoue N Isobe M Itoh K Kaneko O Kawahata K Khlopenkov K Komori A Kubo S Kumazawa R Liang Y Masuzaki S Minami T Miyazawa J Morisaki T Morita S Mutoh T Muto S Nagayama Y Nakanishi H Nishimura K Noda N Notake T Kobuchi T Ohdachi S Ohkubo K Oka Y Osakabe M Ozaki T Pavlichenko RO Peterson BJ Sagara A Saito K Sakakibara S Sakamoto R 《Physical review letters》2001,86(23):5297-5300
Recent large helical device experiments revealed that the transition from ion root to electron root occurred for the first time in neutral-beam-heated discharges, where no nonthermal electrons exist. The measured values of the radial electric field were found to be in qualitative agreement with those estimated by neoclassical theory. A clear reduction of ion thermal diffusivity was observed after the mode transition from ion root to electron root as predicted by neoclassical theory when the neoclassical ion loss is more dominant than the anomalous ion loss. 相似文献
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Narihara K Watanabe KY Yamada I Morisaki T Tanaka K Sakakibara S Ida K Sakamoto R Ohyabu N Ashikawa N Emoto M Funaba H Goto M Hayashi H Idei H Ikeda K Inagaki S Inoue N Kaneko O Kawahata K Kobuchi T Komori A Kubo S Kumazawa R Masuzaki S Miyazawa J Morita S Motojima O Murakami S Muto S Mutoh T Nagayama Y Nakamura Y Nakanishi H Nishimura K Noda N Notake T Ohdachi S Oka Y Ohkubo K Osakabe M Ozaki S Peterson BJ Sagara A Saito K Sasao H Sasao M Sato K Sato M Seki T Shimozuma T Shoji C Sudo S 《Physical review letters》2001,87(13):135002
It was observed that the vacuum magnetic island produced by an external error magnetic field in the large helical device shrank in the presence of plasma. This was evidenced by the disappearance of flat regions in the electron temperature profile obtained by Thomson scattering. This island behavior depended on the magnetic configuration in which the plasmas were produced. 相似文献
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K. Toi K. Oba Y. Maeda T. Ito T. Shirakawa I. Ikemoto T. Tokuda 《Journal of Polymer Science.Polymer Physics》1986,24(1):121-131
The precise pressure dependence of apparent diffusion and permeation coefficients was measured by using a microcomputer system for collecting and treating permeation data for CO2 in glassy poly(ethylene terephthalate) below 1 atm between 15 and 40°C. The partial immobilization model was used to determine the dual-mode sorption and mobility parameters. The curves calculated with these parameters were in excellent agreement with experimental data. These parameters were also compared with sorption parameters obtained from measurements at 30°C. There was a small difference between the values of the parameters obtained from these permeation data and those from sorption data which we had previously obtained. Relations between this difference and the method of determination of the parameters are discussed. 相似文献
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Density modulation experiments are successfully conducted on HT-7 ohmic discharge to investigate particle transport coefficients: diffusion coefficients D and convection velocity V. The particle transport is studied at low (1.5×1019m-3) and high (3×1019 m-3) density regimes. The clear differences are observed that D is 0.42m2/s and 0.17m2/s, V is 4.7m/s (outward) and 1.6 m/s (inward) for low and high density plasmas respectively, where spatially constant D and V(r) = (r/a)V0 were assumed for the analysis. 相似文献
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Keio Toi Tomoyasu Ito Isao Ikemoto Tetsuo Kasai 《Journal of Polymer Science.Polymer Physics》1992,30(5):497-503
Sorption rate curves of CO2, N2, and He gases below 1 atm were measured for polyimide films prepared from benzophenone tetracarboxylic dianhydride (BTDA) with 3,5-diaminotoluene trifluoride (DATF), 2,4-diaminotoluene (DAT), m-phenylenediamine (MPD), and diaminobenzoic acid (DABA). The molecular structures of these four polyimides differ only in the substituent groups of the diamine structure. These polyimides exhibit dualmode type sorption isotherms for carbon dioxide that are concave to the pressure axis, typical of glassy polymer/gas system. The apparent diffusion coefficients below 1 atm pressure of carbon dioxide for this series of compounds decrease in the order: BTDA-DATF > BTDA-DAT > BTDA-MPD > BTDA-DABA. A linear relation between the logarithm of the apparent diffusion coefficient and the reciprocal of free volume, calculated by the method of Bondi using density data, is found for these polyimides. However, this tendency is not observed for the other two gases. The activation energies of the apparent diffusion coefficients at 20 cmHg pressure of carbon dioxide increase with increasing cohesive energy density of the polyimides. The energy per mole of free volume elements in a liquidlike structure in each cohesive energy density may be equated to the activation energy and used to calculate the free volume. The values from the activation energy are almost the same as those from Bondi's method. 相似文献