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81.
Ryu Sasaki 《Czechoslovak Journal of Physics》2003,53(11):1111-1117
The relationship (resemblance and/or contrast) between quantum and classical integrability in Ruijsenaars-Schneider (R-S) and Calogero-Moser systems is addressed. The classical Calogero and Sutherland systems (based on any root system) at equilibrium have many remarkable properties; for example, the minimum energies, frequencies of small oscillations and the eigenvalues of Lax pair matrices at equilibrium are all integer valued. These are related to the energy eigenvalues of the quantum Calogero and Sutherland systems. Similar features and results hold for the R-S type of integrable systems based on the classical root systems. 相似文献
82.
Photoelectrochemical decomposition of water on nanocrystalline BiVO4 film electrodes under visible light 总被引:1,自引:0,他引:1
Sayama K Nomura A Zou Z Abe R Abe Y Arakawa H 《Chemical communications (Cambridge, England)》2003,(23):2908-2909
The nanocrystalline BiVO4 film electrode on conducting glass showed an excellent efficiency (IPCE = 29% at 420 nm) for the decomposition of water under visible light. 相似文献
83.
Studer A Amrein S Matsubara H Schiesser CH Doi T Kawamura T Fukuyama T Ryu I 《Chemical communications (Cambridge, England)》2003,(10):1190-1191
4-[(Trimethylstannyl)diphenylsilyl]butanoyl radical, arising from the corresponding 3-(stannylsilyl)propyl radical and CO, undergoes an SHi reaction at Si with extrusion of trimethyltin radical to give silacyclopentanone. The parent 3-(stannylsilyl)propyl radical was also found to isomerize to (3-stannylpropyl)silyl radical via a 1,4-Sn shift from Si to C with a rate constant of 9.3 x 10(4) s-1 at 80 degrees C. Ab initio and DFT MO calculations support a front-side attack mechanism. 相似文献
84.
Koike R Motoyoshiya J Takaguchi Y Aoyama H 《Chemical communications (Cambridge, England)》2003,(6):794-795
A kinetic study of peroxyoxalate chemiluminescence reactions employing 2,4,6-trichlorophenyl N-aryl-N-tosyloxamates supports the 1,2-dioxetanones still bearing the eliminating group as the key intermediates that interact with the fluorophores rather than 1,2-dioxetanedione. 相似文献
85.
Yamasaki R Tanatani A Azumaya I Saito S Yamaguchi K Kagechika H 《Organic letters》2003,5(8):1265-1267
[reaction: see text] Introduction of an electron-withdrawing group on the aromatic ring of N-methylacetanilide decreased the ratio of the cis conformer, and the ratio correlates well with the Hammett sigma values of the substituents. These steric properties can be applied to achieve amide conformational switching by protonation at the aromatic substituent of 4-[bis(dimethylamino)]-N-methylacetanilide or N-[p-(dimethylamino)phenyl]-N-phenylacetamide. 相似文献
86.
Ahn YH Park EJ Cho K Kim JY Ha SH Ryu SH Yoo JS 《Rapid communications in mass spectrometry : RCM》2004,18(20):2495-2501
The enrichment of phosphopeptides using immobilized metal ion affinity chromatography (IMAC) and subsequent mass spectrometric analysis is a powerful protocol for detecting phosphopeptides and analyzing their phosphorylation state. However, nonspecific binding peptides, such as acidic, nonphosphorylated peptides, often coelute and make analyses of mass spectra difficult. This study used a partial chemical tagging reaction of a phosphopeptide mixture, enriched by IMAC and contaminated with nonspecific binding peptides, following a modified beta-elimination/Michael addition method, and dynamic mass analysis of the resulting peptide pool. Mercaptoethanol was used as a chemical tag and nitrilotriacetic acid (NTA) immobilized on Sepharose beads was used for IMAC enrichment. The time-dependent dynamic mass analysis of the partially tagged reaction mixture detected intact phosphopeptides and their mercaptoethanol-tagged derivatives simultaneously by their mass difference (-20 Da for each phosphorylation site). The number of new peaks appearing with the mass shift gave the number of multiply phosphorylated sites in a phosphopeptide. Therefore, this partial chemical tagging/dynamic mass analysis method can be a powerful tool for rapid and efficient phosphopeptide identification and analysis of the phosphorylation state concurrently using only MS analysis data. 相似文献
87.
Ki-Young Choi Seung-Man Yang Kyu-Chul Lee Haiil Ryu Chan Hee Lee Jungho Seo Mancheol Suh 《Transition Metal Chemistry》2008,33(1):99-105
The tridentate ligand 2-Oximino-3-thiosemicarbazone-2,3-butanedione (Hotsb) reacts with MCl2 (M = Ni2+ or Cu2+) to give rise to the mononuclear complexes [Ni(Hotsb)2]Cl2 · H2O (1) and [Cu(Hotsb)Cl2] · H2O (2). These complexes have been characterized by X-ray crystallography, spectroscopy, and cyclic voltammetry. The nickel(II) ion
in (1) is in a six-coordinate octahedral environment being bonded to the two protonated tridentate ligands which occupy mer positions. The copper(II) ion in (2) is in a five-coordinate square-pyramidal geometry, in which the basal plane is made up the two nitrogens, sulfur, and chloride
atom, while the other chloride atom is coordinated at the axial position. The cyclic voltammogram of the complexes displays
two one-electron waves corresponding to MII/MIII and MII/MI processes. The electronic as well as infrared spectral properties of the title complexes are reported and discussed. 相似文献
88.
Kyukwan Zong Seung Il Shin Dong Ju Jeon Jung No Lee Eung K. Ryu 《Journal of heterocyclic chemistry》2000,37(1):75-78
3‐Aryl‐4‐methoxycarbonylisoxazoles were prepared from the reaction of a variety of substituted benzonitrile oxides with methyl 3‐(p‐nitrobenzoyloxy)acrylate in moderate to good yields. 相似文献
89.
Yanghyun?ByunEmail author Dosang?Joe Jeong?Seog Ryu Seunghun?Yi 《Mathematische Zeitschrift》2003,245(3):435-453
We investigate the possibility of a Lagrangian Whitney trick, a process to remove a pair of intersection points of a self-transverse Lagrangian immersion by a homotopy through Lagrangian immersions. There is a model for which a Lagrangian Whitney trick with compact support works assuming the model satisfies an area-capacity condition. Reduction of more general cases to the model, not necessarily fulfilling the area-capacity requirement, is possible if the given pair of double points admits a suitable symplectic disc and a certain Maslov-Viterbo index is 1. We look into an example to see the actualities of the Maslov-Viterbo index and the area-capacity conditions.
The authors would like to thank the anonymous referee whose suggestions improved remarkably the exposition of the paper. This work was supported by the grant no.R01-2000-000-00004-0 from Korea Science & Engineering Foundation. 相似文献
90.
Hwang S Lee KH Ryu GH Jang YH Lee SB Lee WY Hong JI Chung DS 《The Journal of organic chemistry》2000,65(2):536-542
The binding affinity and selectivity of a new ionophore, [1(8)]starand (1), toward alkali metal cations in methanol were examined through NMR titration experiments and free energy perturbation (FEP) and molecular dynamics simulations. The preference was determined to be K(+) > Rb(+) > Cs(+) > Na(+) > Li(+) in both FEP simulations and NMR experiments. The FEP simulation results were able to predict the relative binding free energies with errors less than 0.13 kcal/mol, except for the case between Li(+) and Na(+). The cation selectivity was rationalized by analyzing the radial distribution functions of the M-O and M-C distances of free metal cations in methanol and those of metal-ionophore complexes in methanol. 相似文献