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91.
Kobayashi M Matsuo T Fukunaga T Hashizume D Fueno H Tanaka K Tamao K 《Journal of the American Chemical Society》2010,132(43):15162-15163
π-Conjugated disilenes with 2-naphthyl or 2-fluorenyl groups on the silicon atoms have been synthesized as air-stable emissive red solids using the bulky 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl (Eind) groups. The strong π-π* absorptions and distinct emission at room temperature, both in solution and in the solid state, have been observed due to the substantial contribution of the 3p(π)*(Si-Si)-2p(π)*(carbon π-electron system) conjugation. 相似文献
92.
Ikuko Mori Miyuki Ukachi Kimiyo Nagano Hiroyasu Ito Jun Yoshinaga Masataka Nishikawa 《Analytical and bioanalytical chemistry》2010,397(2):463-470
A candidate environmental certified reference material (CRM) for the determination of multielements in tea leaves and materials
of similar matrix, NIES CRM No. 23 Tea Leaves II, has been developed and characterized by the National Institute for Environmental
Studies (NIES), Japan. The origin of the material was tea leaves, which were ground, sieved through a 106-μm mesh, homogenized,
and then subdivided into amber glass bottles. The results of homogeneity and stability tests indicated that the material was
sufficiently homogeneous and stable for use as a reference material. The property values of the material were statistically
determined based on chemical analyses by a network of laboratories using a wide range of methods. Sixteen laboratories participated
in the characterization, and nine certified values and five reference values were obtained. These property values of the candidate
CRM, which are expressed as mass fractions, were close to the median and/or mean values of the mass fractions of elements
in various tea products. The candidate CRM is appropriate for use in analytical quality control and in the evaluation of methods
used in the analysis of tea and materials of similar matrix. 相似文献
93.
Akiko Hori Kohei Naganuma 《Acta Crystallographica. Section C, Structural Chemistry》2010,66(5):o256-o259
In the crystal structures of the fully and partially fluorinated flavone derivatives 5,6,7,8‐tetrafluoro‐2‐(2,3,4,5,6‐pentafluorophenyl)‐4H‐1‐benzopyran‐4‐one, C15HF9O2, (I), and 5,6,7,8‐tetrafluoro‐2‐phenyl‐4H‐1‐benzopyran‐4‐one, C15H6F4O2, (II), the pentafluorophenyl group and the pyranone moiety in (I) are twisted due to repulsion of the F substituents, and a CO(δ−)...π(δ+) intermolecular interaction is observed between the carbonyl O atom and the pentafluorophenyl group. In (II), on the other hand, the phenyl group and the pyranone moiety are almost coplanar, and arene–perfluoroarene interactions are observed in the head‐to‐tail intermolecular columnar stacking between the phenyl group and the tetrafluorophenylene moiety. 相似文献
94.
Nishiyama K Kobayasi KI Riquimaroux H 《The Journal of the Acoustical Society of America》2011,130(6):4148-4157
The vocalization behavior of Mongolian gerbils, a model animal of auditory physiology, was examined. A pair of gerbils was placed in a chamber, and their species-specific vocalizations and locomotive behaviors were recorded and analyzed. Two types of calls were predominantly produced: high-frequency upward frequency-modulated (HU-FM) calls and low-frequency multi-harmonic frequency-modulated (LM-FM) calls. Emission rates of HU-FM calls significantly decreased as the distance between the two gerbils increased, and playback of simulated HU-FM calls increased the emission rates. Acoustic analysis of HU-FM calls showed that the calls exhibited a stereotypic spectro-temporal structure including a fixed inter-onset interval (100-175 ms) and that individual differences in the frequency could convey the body size of the callers. The timing of HU-FM calls was highly synchronized with jump movements when an animal vocalized while jumping, suggesting the existence of tight locomotor-vocal coupling. Conversely, LM-FM calls were observed only when the gerbils tactilely contacted with each other while fighting over a food. These results suggest that Mongolian gerbils change the rates of call emissions and call types (e.g., LM-FM or HU-FM calls) in response to changes in visual and possibly tactile and auditory information. The functions of both calls are discussed in terms of their acoustic structures. 相似文献
95.
We study the permutation complexity of finite-state stationary stochastic processes based on a duality between values and orderings between values. First, we establish a duality between the set of all words of a fixed length and the set of all permutations of the same length. Second, on this basis, we give an elementary alternative proof of the equality between the permutation entropy rate and the entropy rate for a finite-state stationary stochastic processes first proved in [J.M. Amigó, M.B. Kennel, L. Kocarev, The permutation entropy rate equals the metric entropy rate for ergodic information sources and ergodic dynamical systems, Physica D 210 (2005) 77-95]. Third, we show that further information on the relationship between the structure of values and the structure of orderings for finite-state stationary stochastic processes beyond the entropy rate can be obtained from the established duality. In particular, we prove that the permutation excess entropy is equal to the excess entropy, which is a measure of global correlation present in a stationary stochastic process, for finite-state stationary ergodic Markov processes. 相似文献
96.
97.
Yasuharu Yoshimi Kosuke Kobayashi Keisuke Nishikawa Kousuke Maeda Tatsuya Itou Minoru Hatanaka 《Tetrahedron letters》2010,51(17):2332-6179
Radical addition to a glyoxylic oxime ether was accomplished under mild conditions using an alkyl radical generated from a free carboxylic acid via photochemical decarboxylation. The photoreaction provided an efficient route to α-substituted α-aminoesters from carboxylic acids and oxime ether. 相似文献
98.
Daiki Fujise Kiyomi Tsuji Naoko Fukushima Kohei Kawai Ken-ichi Harada 《Journal of chromatography. A》2010,1217(39):6122-6125
In order to fully understand the role of volatile organic compounds (VOCs) under natural conditions, an adaptable analytical method was developed as the first step. β-Ionone, β-cyclocitral, 2-methyl-1-butanol and 3-methyl-1-butanol were simultaneously analyzed in addition to geosmin and 2-MIB using GC/MS with SPME. The slight modification of a known method allowed the simultaneous detection and quantification of these VOCs. The SIM of the 3-methyl-1-butanol was always accompanied by a shoulder peak, suggesting the presence of two compounds. In order to separate both compounds, the GC/MS conditions were optimized, and the additional peak was identified as 2-methyl-1-butanol by direct comparison of the authentic compound, indicating that the Microcystis strain always produces a mixture of 2-methyl-1-butanol and 3-methyl-1-butanol. Furthermore, it was found that 2-methyl-1-butanol and 3-methyl-1-butanol were predominant in the dissolved fractions. β-Cyclocitral was easily oxidized to provide the oxidation product, 2,6,6-trimethylcyclohexene-1-carboxylic acid, which causes the blue color formation of cyanobacteria as a consequence of acid stress. The intact acid could be satisfactorily analyzed using the usual GC/MS without derivatization. 相似文献
99.
Hidemi Nagao Masayoshi Nakano Kiyoshi Nishikawa Kizashi Yamaguchi 《International journal of quantum chemistry》2001,84(4):401-408
We investigate the quantum dynamics of two‐boson and two‐level systems interacting with a one‐mode photon field. The time evolution of the population for each state is calculated in terms of the Jaynes–Cummings model. We find the collapses and revivals of the order parameter for the Bose–Einstein condensation. © 2001 John Wiley & Sons, Inc. Int J Quantum Chem 84: 401–408, 2001 相似文献
100.
Polycatenar materials composed of a four-aromatic-ring core, with either a bulky or end-branched perfluorinated moiety attached at one end through a methylene spacer group, and three peripheral alkoxy chains of varying length (the carbon number n = 4, 6, 8, 10, 12, 14, 16) on the other end-ring, were synthesized to investigate the roles of the chemical structure of the compositional segments in relation to liquid crystalline phase formation. It was found that a homologous series of polycatenar materials exhibited a variety of liquid crystalline phases strongly dependent on the length of the peripheral alkyl chains. Moreover it was shown that changes in the spacer group and in the structure of the perfluorinated segment had a significant influence on mesophase formation. 相似文献