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81.
The null result in the LHC may indicate that the standard model is not drastically modified up to very high scales, such as the GUT/string scale. Having this in the mind, we suggest a novel leptogenesis scenario realized in the false vacuum of the Higgs field. If the Higgs field develops a large vacuum expectation value in the early universe, a lepton number violating process is enhanced, which we use for baryogenesis. To demonstrate the scenario, several models are discussed. For example, we show that the observed baryon asymmetry is successfully generated in the standard model with higher-dimensional operators. 相似文献
82.
The secondary radiation after resonant excitation of F center and its linear polarization P correlated to the polarization of resonant light have been measured for five alkali halides at low temperatures. In KC1, the spectrum of P over the whole Stokes region is divided into three successive regions, the depolarization range at the one-phonon Raman scattering, the near plateau range, and the depolarization range down to vanishing. The former two have common relevance to resonant energy and symmetries of coupled phonons. These relevances are interpreted adopting a configuration coordinate model for 2s- and 2p-like excited states. 相似文献
83.
Tomoya Ito Koji Suda Takuya Kumamoto Waka Nakanishi Toshiko Watanabe Tsutomu Ishikawa Hiroko Seki Masatoshi Kawahata Kentaro Yamaguchi Yasumitsu Ogura Kazuo T. Suzuki 《Molecular diversity》2010,14(1):131-145
The role of o-bisguanidinobenzenes (BGBs) as new Brønsted base ligands for arsenic and phosphoric acids was examined. In solution state, complexation was evaluated by Job’s plot in 1H NMR experiment, indicating a 1:1 complex formation, whereas in solid state crystalline structures of complexes obtained were addressed by X-ray crystallographic analysis and/or solid state 13C NMR experiment, in which 1:2 complexes between the BGB and the acid components were normally formed. Based on these results, Merrifield and Hypogel® resin-anchored BGBs were designed and prepared as the corresponding polymer-supported host ligands. Evaluation of their coordination ability with metal salts (ZnCl2 and CoCl2) and arsenic acid in aqueous media by ICP-MS showed that the latter Hypogel® resin-anchored BGBs acted as effective immobilized base ligands. 相似文献
84.
Kinetic equations for the one-particle distribution function of dilute gases and plasmas and evolution equations for the variance of their fluctuations are obtained from the BBGKY hierarchy equations by using Mori's scaling method in an extended form. 相似文献
85.
Harry Adams Neil A. Bailey David E. Fenton Choki Fukuhara Masatoshi Kanesato 《Supramolecular chemistry》2013,25(4):325-330
Abstract The synthesis and crystal structure of the diprotonated cryptand derived from the reaction of tren and 2,6-diacetyl pyridine is reported. The imino nitrogens of the Schiff base linkages are directed so that the dicarbimine functions are in trans, trans geometry relative to the pyridine C-N bond. This configuration has not previously been reported in related pyridine-derived Schiff base macrocycles. 相似文献
86.
Tatsuya Mori ATLAS Liquid Argon Calorimeter Group 《Physics of Particles and Nuclei Letters》2016,13(5):541-546
This article gives an overview of the Phase-I Upgrade of the ATLAS LAr Calorimeter Trigger Readout. The design of custom developed hardware for fast real-time data processing and transfer are presented. Performance results from the prototype boards operated in the demonstrator system, first measurements of noise behavior and responses on the test pulses to the demonstrator system are shown. 相似文献
87.
Kunihiro Ichimura Masatoshi Kidowaki Haruhisa Akiyama Kazuaki Kudo Veronika Strehmel Bernd Strehmel 《Macromolecular rapid communications》1996,17(8):545-551
The surface-assisted alignment of a nematic liquid crystal yields a persistent ordered structure upon cationic photopolymerization of liquid-crystalline epoxides. Linearly polarized light irradiation of a photocrosslinkable polymer containing azobenzene moieties played a crucial role in this procedure since the photoinduced alignment is not deteriorated by heating for polymerization. 相似文献
88.
Tsuneo Imamoto Masatoshi Matsuo Taro Nonomura Kuniyuki Kishikawa Masao Yanagawa 《Heteroatom Chemistry》1993,4(5):475-486
Cyclohexyl(o-methoxyphenyl)menthyloxyphosphineborane and t-butyl(o-methoxyphenyl)menthyloxyphosphine-borane were prepared from dichlorocyclohexylphosphine and t-butyldichlorophosphine by successive treatments with (−)-menthol, o-methoxyphenylmagnesium bromide, and borane-THF complex. The separated pure diastereomers of each of the compounds underwent reaction with lithium naphthalenide to afford optically pure cyclohexyl(o-methoxyphenyl)phosphine-borane and t-butyl(o-methoxyphenyl)phosphine-borane, respectively. These secondary phosphine-boranes reacted readily with various electrophiles in the presence of bases with virtually net retention of configuration. A new chiral phosphine ligand, (S,S)-1,2-bis[cyclohexyl(o-methoxyphenyl)phosphino]ethane was synthesized via the optically pure phosphine-boranes. 相似文献
89.
Tooru Ooya Hideharu Mori Minoru Terano Nobuhiko Yui 《Macromolecular rapid communications》1995,16(4):259-263
A novel design of a biodegradable carrier for drug delivery was established by constructing a supramolecular assembly of drugs and polymer backbones without any covalent bonds. A biodegradable polyrotaxane was synthesized in which α-cyclodextrins (α-CDs) as drug carriers were threaded onto poly(ethylene glycol) chains which then were capped at each chain end by L -phenylalanine via peptide linkages. The release of α-CDs was observed only when the terminal peptide linkages were degraded. 相似文献
90.
Yoshio Okamoto Tamaki Nakano Yoshifumi Shikisai Masatoshi Mori 《Macromolecular Symposia》1995,89(1):479-488
Stereospecific and asymmetric (helix-sense-selective) polymerization of 1-phenyldibenzosuberyl methacrylate (PDBSMA) was performed with radical and anionic initiators. A highly isotactic polymer having triad isotacticity greater than 97% was obtained by radical polymerization with (i-PrOCOO)2 at 40°C. The radical polymerization of PDBSMA in (+)- and (-)-menthol gave (-)-and (+)-polymers, respectively, whose optical activity is ascribed to the prevailing one-handed helical conformation of a polymer chain. The radical copolymerization of PDBSMA with a small amount of an optically active monomer, (+)-phenyl-2-pyridyl-o-tolylmethyl methacrylate, afforded an optically active copolymer with the prevailing one-handed helical structure of PDBSMA sequences. Asymmetric anionic polymerization of PDBSMA was carried out with the complex of N, N′-diphenylethylenediamine monolithium amide and a chiral ligand, (+)-1-(2-pyrrolidinylmethyl)pyrrolidine in toluene at −78°C. The obtained polymer was highly isotactic and optically active due to nearly 100% one-handed helical structure. 相似文献