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51.
We study rule induction from two decision tables as a basis of rough set analysis of more than one decision tables. We regard the rule induction process as enumerating minimal conditions satisfied with positive examples but unsatisfied with negative examples and/or with negative decision rules. From this point of view, we show that seven kinds of rule induction are conceivable for a single decision table. We point out that the set of all decision rules from two decision tables can be split in two levels: a first level decision rule is positively supported by a decision table and does not have any conflict with the other decision table and a second level decision rule is positively supported by both decision tables. To each level, we propose rule induction methods based on decision matrices. Through the discussions, we demonstrate that many kinds of rule induction are conceivable. 相似文献
52.
53.
A free-piston shock tunnel (FPST) is one of the most useful ground testing facilities for hypervelocity flow research of re-entry vehicles and scramjet engines. For an efficient operation with tuned piston motion, the design of facility and the comprehension of the physical phenomena in a FPST, a numerical simulation which can properly predicts the flow with actual losses is required. But there are few successful numerical methods which can simulate its overall performance. In the present study, numerical method was developed by using the KRC shock capturing scheme and by modeling the flow losses in suitable forms for a quasi-1D numerical computation. The present numerical results were compared with the data obtained in two different facilities, T4 and T5. The applicability of the present numerical method as a design tool is discussed briefly.This article was processed using Springer-Verlag TEX Shock Waves macro package 1.0 and the AMS fonts, developed by the American Mathematical Society. 相似文献
54.
55.
Li M Ishihara S Akada M Liao M Sang L Hill JP Krishnan V Ma Y Ariga K 《Journal of the American Chemical Society》2011,133(19):7348-7351
Electrochemical-coupling layer-by-layer (ECC-LbL) assembly is introduced as a novel fabrication methodology for preparing layered thin films. This method allows us to covalently immobilize functional units (e.g., porphyrin, fullerene, and fluorene) into thin films having desired thicknesses and designable sequences for both homo- and heteroassemblies while ensuring efficient layer-to-layer electronic interactions. Films were prepared using a conventional electrochemical setup by a simple and inexpensive process from which various layering sequences can be obtained, and the photovoltaic functions of a prototype p/n heterojunction device were demonstrated. 相似文献
56.
Ishihara S Hill JP Shundo A Richards GJ Labuta J Ohkubo K Fukuzumi S Sato A Elsegood MR Teat SJ Ariga K 《Journal of the American Chemical Society》2011,133(40):16119-16126
Porphyrin derivatives bearing 2,6-di-tert-butylphenol substituents at their 5,15-positions undergo reversible photoredox switching between porphyrin and porphodimethene states as revealed by UV-vis spectroscopy, fluorescence spectroscopy, and X-ray single-crystal analyses. Photoredox interconversion is accompanied by substantial variations in electronic absorption and fluorescence emission spectra and a change of conformation of the tetrapyrrole macrocycle from planar to roof-shaped. Oxidation proceeds only under photoillumination of a dianionic state prepared through deprotonation using fluoride anions. Conversely, photoreduction occurs in the presence of a sacrificial electron donor. Transient absorption spectroscopy and electron spin resonance spectroscopy were applied to investigate the processes in photochemical reaction, and radical intermediates were characterized. That is, photooxidation initially results in a phenol-substituent-centered radical, while the reduction process occurs via a delocalized radical state involving both the macrocycle and 5,15-substituents. Forward and reverse photochemical processes are governed by different chemical mechanisms, giving the important benefit that conversion reactions are completely isolated, leading to better separation of the end states. Furthermore, energy diagrams based on electrochemical analyses (cyclic voltammetry) were used to account for the processes occurring during the photochemical reactions. Our molecular design indicates a simple and versatile method for producing photoredox macrocyclic compounds, which should lead to a new class of advanced functional materials suitable for application in molecular devices and machines. 相似文献
57.
Kikura-Hanajiri R Kawamura M Miyajima A Sunouchi M Goda Y 《Analytical and bioanalytical chemistry》2011,400(1):165-174
In order to develop an analytical method for the discrimination of dextromethorphan (an antitussive medicine) from its enantiomer,
levomethorphan (a narcotic) in biological samples, chiral analyses of these drugs and their O-demethyl and/or N-demethyl metabolites in rat plasma, urine, and hair were carried out using LC-MS/MS. After the i.p. administration of dextromethorphan
or levomethorphan to pigmented hairy male DA rats (5 mg/kg/day, 10 days), the parent compounds and their three metabolites
in plasma, urine and hair were determined using LC-MS/MS. Complete chiral separation was achieved in 12 min on a Chiral CD-Ph
column in 0.1% formic acid–acetonitrile by a linear gradient program. Most of the metabolites were detected as being the corresponding
O-demethyl and N, O-didemethyl metabolites in the rat plasma and urine after the hydrolysis of O-glucuronides, although obvious differences in the amounts of these metabolites were found between the dextro and levo forms.
No racemation was observed through O- and/or N-demethylation. In the rat hair samples collected 4 weeks after the first administration, those differences were more clearly
detected and the concentrations of the parent compounds, their O-demethyl, N-demethyl, and N, O-didemethyl metabolites were 63.4, 2.7, 25.1, and 0.7 ng/mg for the dextro forms and 24.5, 24.6, 2.6, and 0.5 ng/mg for the
levo forms, respectively. In order to fully investigate the differences of their metabolic properties between dextromethorphan
and levomethorphan, DA rat and human liver microsomes were studied. The results suggested that there might be an enantioselective
metabolism of levomethorphan, especially with regard to the O-demethylation, not only in DA rat but human liver microsomes as well. The proposed chiral analyses might be applied to human
samples and could be useful for discriminating dextromethorphan use from levomethorphan use in the field of forensic toxicology,
although further studies should be carried out using authentic human samples. 相似文献
58.
Ishida Y Shimada T Masui D Tachibana H Inoue H Takagi S 《Journal of the American Chemical Society》2011,133(36):14280-14286
The quantitative excited energy transfer reaction between cationic porphyrins on an anionic clay surface was successfully achieved. The efficiency reached up to ca. 100% owing to the "Size-Matching Rule" as described in the text. It was revealed that the important factors for the efficient energy transfer reaction are (i) suppression of the self-quenching between adjacent dyes, and (ii) suppression of the segregated adsorption structure of two kinds of dyes on the clay surface. By examining many different kinds of porphyrins, we found that tetrakis(1-methylpyridinium-3-yl) porphyrin (m-TMPyP) and tetrakis(1-methylpyridinium-4-yl) porphyrin (p-TMPyP) are the suitable porphyrins to accomplish a quantitative energy transfer reaction. These findings indicate that the clay/porphyrin complexes are promising and prospective candidates to be used for construction of an efficient artificial light-harvesting system. 相似文献
59.
Yamaguchi K Ueki R Nonaka H Sugihara F Matsuda T Sando S 《Journal of the American Chemical Society》2011,133(36):14208-14211
Monoamine oxidase (MAO) A is a flavoenzyme that catalyzes the oxidation of biologically important monoamines and is thought to be associated with psychiatric disorders. Here, we report a strategy for rationally designing a (19)F magnetic resonance imaging probe for the specific detection of human MAO-A (hMAO-A) activity. Our designed (19)F probe was oxidized expeditiously by hMAO-A to produce 2-fluoro-4-nitrophenol via a spontaneous β-elimination mechanism. Concomitant with the structural change of the probe to the product, the (19)F chemical shift changed by 4.2 ppm, which was enough to visualize the probe and enzymatic product separately. Importantly, our probe achieved excellent discrimination of hMAO-A from its isoform hMAO-B. 相似文献
60.
Enantioselective total synthesis of the biologically important indole alkaloids (+)-lysergol, (+)-isolysergol, and (+)-lysergic acid is described. Key features of these total synthesis include (1) a facile synthesis of a chiral 1,3-amino alcohol via the Pd(0)- and In(I)-mediated reductive coupling reaction between L-serine-derived 2-ethynylaziridine and formaldehyde; (2) the Cr(II)/Ni(0)-mediated Nozaki-Hiyama-Kishi (NHK) reaction of an indole-3-acetaldehyde with iodoalkyne; and (3) Pd(0)-catalyzed domino cyclization of an allene bearing amino and bromoindolyl groups. This domino cyclization enabled direct construction of the C/D ring system of the ergot alkaloids skeleton, as well as the creation of the C5 stereogenic center with transfer of the allenic axial chirality to the central chirality. 相似文献