Analysis of the3 He(K−,K +)n reaction by the potential quark model

We analyze the production of H dihyperson (J ^π=0⁺,S=?2) via the (K ^?, K⁺) reaction by means of the non-relativistic quark model. First, the H mass and mass spectrum of single baryons are calculated. When the single baryon spectrum is well reproduced, the H dihyperson has the binding energies about 20 MeV or 60 MeV corresponding to the choice of the strength of the confinement potential. Using this model and parameters, cross sections for H production are estimated. A new effect, contributions from color-octetQ ³?Q ³ components of H dihyperson, is taken into account. The cross sections for H production are enhanced about ten times by these contributions. TheK ⁺-neutron coincidence cross section for H production is found to be 99–115 nb/sr² at theK ⁺ forward direction forM _H=2212 MeV and theK ^? beam momentum 1.8 GeV/c.     

Super-effective-field theory and coherent-anomaly method in cooperative phenomena

Conceptual arguments on the coherent-anomaly method (CAM) and on the super-effective-field theory are presented to explain the basic ideas of these theories. Some possible applications are also suggested.     

Biospecific thermal analyzer coupled with a flowthrough immobilized enzyme column

A thermal analyzer consisting of a pair of glass thermistors was coupled with a flowthrough immobilized enzyme reactor for the determination of ATP concentration. Hexokinase was covalently bound to poly(chloromethyl-styrene-divinyl benzene) beads and packed in the reactor. The thermal analyzer was designed so as to respond to heat generation in the reactor. A maximum temperature change was exhibited within 1.5 min after the injection of a sample solution containing ATP together with glucose. Thermal decay occurred within 1 min. The thermal analyzer responded reproducibly to ATP at a constant concentration. Assays could be repeated at 3-min intervals. The effects of sample volume and flow rate on the response were examined with regard to an empirical equation. Concentration of ATP was determined with the thermal analyzer in the range of 0-10 mM. The thermal analyzer may be a simple device for the rapid determination of ATP concentration.     

On the convergence of exponential operators—the Zassenhaus formula,BCH formula and systematic approximants

The convergence of the Zassenhaus formula is proven under an appropriate condition as well as for other exponential operators such as the Baker-Campbell-Hausdorff formula.On leave of absence from Department of Physics, Faculty of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan     

Mechanism of stigmasterol dealkylation in insect

Deuterated stigmasterols (10, 11 and 12) were chemically synthesized and fed to silk-worm larvae. GC-MS analysis of the metabolites, cholesterol (4) and desmosterol (6), indicates the migration of 25-hydrogen to C-24 position during stigmasterol dealkylation. 22,24(28)-Dienes(8a and 8b) were shown to be converted to 22,24-diene (5), desmosterol and cholesterol.     

1-vinylbenzene 1,2- and 3,4-oxides

Synthesis of highly unstable vinyl-substituted benzene oxides has been established.     

121Sb Mössbauer spectroscopic study on electronic states of pentavalent organoantimony compounds

A systematic study of pentavalent organoantimony compounds, (RC₆H₄)₃SbX₂ (R=H,p-CH₃,p-F,p-Cl,p-CF₃,o-CH₃; X=Cl, Br), was carried out to examine the effect on Mössbauer parameters of the substituent on the aromatic ring. The Mössbauer parameters obtained in polycrystalline form reflected the steric effect caused by the position of the substituent on the aromatic ring. On the other hand, measurements in frozen organic solutions revealed that the electron density and electric field gradient at and around the antimony nucleus became smaller when the more electron-attractive group was introduced into thepara position.     

Biferrocene-M(mnt)2 charge-transfer complexes (M = Ni, Co; mnt = maleonitriledithiolate). structure, valence states, and magnetic properties

Charge-transfer salts of branched-alkyl biferrocenes, (1',1' '-R2-1,1' '-biferrocene)[Ni(mnt)2] (1a, R = isopropyl; 2a, R = dineopentyl) and (1',1' '-R2-1,1' '-biferrocene)2[Co(mnt)2]2 (1b, R = isopropyl; 2b, R = dineopentyl), were prepared. Their valence states were investigated using X-ray crystallography and M?ssbauer spectroscopy. Complexes 1a and 1b show segregated-stack crystal structures that contain columns of acceptors, whereas structures of 2a and 2b, which contain bulky donors, are rather discrete. All of the complexes contain mixed-valent biferrocenium monocations. A two-step valence transition was found in complex 1a. The crystal contains two crystallographically independent cations: one undergoes valence localization below room temperature; the other undergoes valence localization below ca. 130 K. The former transition is derived from asymmetry of the crystal environment around the cation, whereas the latter one is caused by symmetry lowering coupled with a spin-Peierls transition (T(C) = 133.2 K) associated with the dimerization of the acceptors. This compound was found to exhibit a dielectric response based on valence tautomerization. Other complexes (1b, 2a, and 2b) show a valence-trapped state. In all complexes, charge localization was found to occur through local electrostatic interactions between the donor's cationic moiety and the acceptor's electronegative moieties.     

Temperature dependence of local density augmentation for acetophenone N,N,N',N'-tetramethylbenzidine exciplex in supercritical water

Local density augmentation around exciplex between acetophenone and N,N,N',N'-tetramethylbenzidine in supercritical water was measured by observing the peak shift of transient absorption spectrum at temperatures from 380 to 410 degrees C and at pressures from 6 to 37 MPa. Large local density augmentation was observed at lower solvent densities. Local density augmentation was evaluated by the excess density, which was defined as the difference between local density and bulk density, and the density enhancement factor, which was defined by the ratio of the local density to the bulk density. The number of solvating molecules was estimated with a Langmuir adsorption model. The excess density was found to exhibit a maximum at approximately 0.15 g cm(-3), which decreased with increasing temperature. The density enhancement factor was found to decrease with increasing temperature; however, its value was much greater than unity at 410 degrees C, which provides evidence that exciplex-water interactions still exist at these conditions. The temperature dependence of local density augmentation around the exciplex in supercritical water was comparable with that in supercritical carbon dioxide, which suggests that the ratios of the solute-solvent and solvent-solvent interactions are comparable between these two systems.