Untersuchungen an funktionellen Mizellen. 1. Mitt. Darstellung von cyclischen Dipeptiden aus Phenylalanin-S-dodecylester

Ohne Zusammenfassung     

Carbon-carbon double bond cleavage with a hard lewis acid and ethanethiol

Double bonds activated by the electron withdrawing group(s) are cleaved with the reagent system consisting of a hard Lewis acid and ethanethiol to give dithioacetals.     

The structures and electronic states of zinc-water clusters Zn(n)(H2O)(m) (n = 1-32 and m = 1-3)

Ab initio and Density Functional Theory (DFT) calculations have been carried out for zinc-water clusters Zn(n)-(H2O)(m) (n = 1-32 and m = 1-3, where n and m are the numbers of zinc atoms and water molecules, respectively) to elucidate the structure and electronic states of the clusters and the interaction of zinc cluster with water molecules. The binding energies of H2O to zinc clusters were small at n = 2-3 (2.3-4.2 kcal mol(-1)), whereas the energy increased significantly in n = 4 (9.0 kcal mol(-1)). Also, the binding nature of H2O was changed at n = 4. The cluster size dependency of the binding energy of H2O accorded well with that of the natural population of electrons in the 4p orbital of the zinc atom. In the larger clusters (n > 20), it was found that the zinc atoms in surface regions of the zinc cluster have a positive charge, whereas those in the interior region have a negative charge with the large electron population in the 4p orbital. The interaction of H2O with the zinc clusters were discussed on the basis of the theoretical results.     

Calyciphylline D, a novel alkaloid with an unprecedented fused-pentacyclic skeleton from Daphniphyllum calycinum

[structure: see text]. Calyciphylline D (1), a novel Daphniphyllum alkaloid with an unprecedented fused-pentacyclic skeleton containing a 8-azatricyclo[4.2.1.0.4,8]nonane ring system, has been isolated from the leaves of Daphniphyllum calycinum (Daphniphyllaceae), and the structure and relative stereochemistry were elucidated on the basis of spectroscopic data.     

Effects of stacking fault energies on formation of irradiation-induced defects at various temperatures in face-centred cubic metals

ABSTRACT

By using the six sets of interatomic potentials for face-centred cubic metals that differ in the stacking fault energy (SFE) while most of the other material parameters are kept almost identical, we conducted molecular dynamics simulations to evaluate the effects of SFE on the defect formation process through collision cascades. The simulations were performed at 100, 300 and 600?K, with a primary knock-on atom energy of 50 keV. The number of residual defects is not dependent on the SFE at all the temperatures. For clusters of self-interstitial atoms (SIAs), their clustering behaviour does not depend on the SFE, either. However, the ratio of glissile SIA clusters tends to decrease with increasing SFE. This is because perfect loops, the edges of which split into two partial dislocations with stacking fault structures between them in most cases, prefer to form at lower SFEs. The enhanced formation of glissile SIA clusters at lower SFEs can also be observed even at increased temperature. Because most large vacancy clusters have stacking fault structures, they preferentially form at lower SFE; however, it is observed only at the lowest temperature, where the mean size increases with decreasing SFE. At higher temperatures, because of their extremely low number density, the vacancy clustering behaviour does not depend on the SFEs.     

Three-state molecular shuttles operated using acid/base stimuli with distinct outputs

This paper describes the acid/base-mediated three-state translational isomerization of two [2]rotaxanes, each containing N-alkylaniline and N,N-dialkylamine centers as binding sites for threaded dibenzo[24]crown-8 units. Under neutral conditions, the dialkylamine unit predominantly recognized the crown ether component through cooperative binding of a proton; when both amino units were protonated under acidic conditions, both translational isomers were generated; the addition of a strong base caused aniline-crown ether interactions to dominate. The three states of the [2]rotaxane featuring the 3,5-diphenylaniline terminus in its dumbbell-shaped component were accompanied by distinct absorptive outputs that were detectable using UV spectroscopy.     

Transition processes from the lamellar to the onion state with increasing temperature under shear flow in a nonionic surfactant/water system studied by Rheo-SAXS

In a previous paper, we reported for the first time the lamellar-to-onion transition with increasing temperature at around 67 °C under a constant shear rate (0.3-10 s(-1)) in a nonionic surfactant C(16)E(7)/water system. In this study, the first temperature-shear rate diagram has been constructed in a wider range of shear rate (0.05-30 s(-1)) than in our previous study based on the temperature dependence of the shear stress at constant shear rate. The results suggest that the critical temperature above which the transition begins does not depend on the shear rate very much, although it takes a very shallow minimum. Then we have performed simultaneous measurements of small-angle X-ray scattering/shear stress (rheo-SAXS) with a stepwise increase in temperature of 0.1 K per 15 min at a constant shear rate of 3 s(-1) near the transition temperature. When the temperature exceeds 67 °C, just before the increase in the shear stress, the intensity of the Bragg peak for the velocity gradient direction (approximately proportional to the number of lamellae with their normal along this direction) is suddenly increased. As the temperature increases by 0.2 K, the shear stress begins to increase. At the same time, the peak intensity in the velocity gradient direction rapidly decreases and instead the intensity in the neutral direction increases. As the temperature increases further, the intensities in both the neutral and gradient directions decrease whereas the intensity in the flow direction increases, corresponding to the formation of onions. We have also performed rheo-SAXS experiments with a stepwise increase in shear rate at 72 °C. The sequence of the change in the intensity in each direction is almost the same in the temperature scan experiments at constant shear rate, suggesting that the transition mechanisms along these two paths are similar. The abrupt enhancement of the lamellar orientation with the layer normal along the velocity gradient direction just before the transition is the first finding and strongly supports the coherent buckling mechanism in the lamellar-to-onion transition proposed by Zilman and Granek (Zilman, A. G.; Granek, R. Eur. Phys. J. B 1999, 11, 593).