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1.
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Yoshio Moriya Shinichi Nakata Hirotaka Morimoto Nobuaki Ogawa 《Analytical sciences》2004,20(11):1533-1536
Analysis by reflection spectrometry was performed to clarify the interfacial adsorption of protonated lipophilic tetraphenylporphyrin derivatives in a dodecane-aqueous sulfuric acid system, and to confirm the utility of partial reflection spectroscopy. Interfacial adsorption was not observed for porphyrins substituted at the 2,6 positions of meso-phenyl groups, suggesting that the substituents prevent porphyrins from forming aggregates by steric hindrance. Polymorphous J-aggregates of acid dications were produced by tetra-p-tolylporphyrin with a saturated interfacial molecular density of 1.0 x 10(-10) mol cm(-2), which could yield 48 degrees as a mean tilting angle of the pyrrole ring plane from the interface normal. Partial-reflection spectrometry can provide sensitive detection and molecular orientation analysis of interfacial adsorbates. 相似文献
3.
In this paper we consider the (t, n)-threshold visual secret sharing scheme (VSSS) in which black pixels in a secret black-white images is reproduced perfectly
as black pixels when we stack arbitrary t shares. This paper provides a new characterization of the (t, n)-threshold visual secret sharing scheme with such a property (hereafter, we call such a VSSS the (t, n)-PBVSSS for short). We use an algebraic method to characterize basis matrices of the (t, n)-PBVSSS in a certain class of matrices. We show that the set of all homogeneous polynomials each element of which yields
basis matrices of the (t, n)-PBVSSS becomes a set of lattice points in an (n−t+1)-dimensional linear space. In addition, we prove that the optimal basis matrices in the sense of maximizing the relative
difference among all the basis matrices in the class coincides with the basis matrices given by Blundo, Bonis and De Santis
[3] for all n≥ t ≥ 2. 相似文献
4.
Suchada Suntornchashwej Dr. Khanit Suwanborirux Dr. Kazushi Koga Minoru Isobe Prof. Dr. 《化学:亚洲杂志》2007,2(1):114-122
Malyngamide X ( 1 ), the first (7R)‐lyngbic acid connected to a new tripeptide backbone, was isolated from the Thai sea hare Bursatella leachii. The gross structure of 1 was established on the basis of 1D and 2D NMR and mass spectroscopic data. Combination of the NMR spectroscopic experiments with α‐methoxy‐α‐(trifluoromethyl)phenylacetic acid esters, 2,2,2‐trifluoro‐1‐(9‐anthryl)ethanol chiral solvating agent, and molecular mechanics of 1 and the synthetic molecular fragments allowed us to determine the absolute stereochemistry of all six stereogenic centers without hydrolytic degradation of the compound. Compound 1 displayed moderate cytotoxic, antitubercular, and antimalarial properties. 相似文献
5.
6.
Simulation of electron bunch generation by an ultrashort-pulse high-intensity laser-driven wakefield
M. Yamagiwa S. V. Bulanov T. Zh. Esirkepov J. Koga M. Kando Y. Ueshima K. Saito D. Wakabayashi 《Laser Physics》2006,16(2):252-258
Electron acceleration due to a wakefield excited by a ultrashort-pulse intense laser propagating through a finite-length underdense plasma layer is studied by two-dimensional particle-in-cell simulation. The electron energy distribution is analyzed for moderate to high intensity. For the electron density, where the pulse length is almost half of the plasma wavelength, dramatic changes of the density structure occur with cavity and bunch formation with an increase in the laser intensity, also leading to the appearance of a fast electron component well confined in phase space. The analytical form of the fast electron energy spectrum is also presented. 相似文献
7.
Junsaku Nitta Yiping Lin Takaaki Koga Tatsushi Akazaki 《Physica E: Low-dimensional Systems and Nanostructures》2004,20(3-4):429
We report on electron g-factor in an InAs-inserted In0.53Ga0.47As/In0.52Al0.48As heterostructure. The gate voltage dependence of g-factor is obtained from the coincidence method. The obtained g-factor values are surprisingly smaller than the g-factor value of bulk InAs, and it is close to the bare g-factor value of In0.53Ga0.47As. The large change in g-factor is observed by applying the gate voltage. The obtained gate voltage dependence is not simply explained by the energy dependence of g-factor. 相似文献
8.
Takuya Hasegawa Hirotaka Matsuura Kazumi Inagaki Hiroki Haraguchi 《Analytical sciences》2003,19(1):147-150
The major-to-ultratrace elements in human bone-marrow fluid were determined by ICP-AES (inductively coupled plasma atomic emission spectrometry), and ICP-MS (inductively coupled plasma mass spectrometry). The bone-marrow fluid sample was centrifuged prior to acid digestion to exclude the bone piece from bone marrow, and then digested with nitric acid. As a result, 20 elements could be determined over the concentration range from 1610 microg g(-1) for Na to 0.00043 microg g(-1) for W. It was found that Fe, Zn and Sb were enriched by ca. 264-, 7- and 15-fold, respectively, in bone-marrow fluid, compared to those in human blood serum. Alkali metals (K, Rb, Cs), except for Na, were also significantly enriched in bone-marrow fluid. Furthermore, the concentrations of various elements, such as Fe, P, Al, Zn, Cu, Se, Zr, Sn, Ag and W, were significantly higher than those in open seawater. 相似文献
9.
10.
Hirotaka Okamoto Tadashi Inoue Kunihiro Osaki 《Journal of Polymer Science.Polymer Physics》1995,33(3):417-424
The complex Young's modulus, E*(ω), and the complex strain-optical coefficient, O*(ω), which is the ratio of the birefringence to the strain, were measured for polyisoprene (PIP) over a frequency range of 1 ~ 130 Hz and a temperature range of 22 ~ ?100°C. The imaginary part of O*, O″, was positive at low frequencies and negative at high frequencies. The real part, O′, was always positive and showed a maximum. The complicated behavior of O* could be understood by the assumption that E* = ER* + EG* and O* = CRER* + CGEG*, where ER* and EG* were complex quantities and CR and CG were constants. The CR value, equal to the ordinary stress-optical coefficient measured in the rubbery plateau zone, was 2.0 × 10?9 Pa?1. The CG value, defined as the ratio O″/E″ in the glassy zone, was ?1.1 × 10?11 Pa?1. The EG*, which was the major component of E* in the glassy zone, showed almost the same frequency dependence as that of polystyrene and polycarbonate. The ER*, which was dominant in the rubbery zone, was described well by the bead-spring theory. The temperature dependence of the EG* was stronger than that of the ER*. This difference caused the breakdown of the thermorheological simplicity for E* and O* around the glass-to-rubber transition zone. © 1995 John Wiley & Sons, Inc. 相似文献