Azulenophanes V synthesis and physical properties of [2](5,7)azuleno[2]para- and metacyclophanes

The title compounds $\text{3}$ and $\text{4}$ were synthesized by the usual dithia[3.3]phane coupling and photodesulfurization route. Investigation of their physical properties established their molecular dimension and conformation. Transannular interaction disclosed by their electronic spectra was explained by MO calculations.     

An anomalous emission excited near the absorption edge of pyrene crystals

Emission spectra and decay times of the fluorescence excited at the absorption edge region in pyrene crystals were measured. At liquid nitrogen temperature, the fluorescence under the excitation at 390 nm is considered as the excimer emission and its band peak shifts a little to the short wavelength in comparison with that of the excimer emission under the excitation at 360 nm. The emission decay times under the excitation at the 390 nm and 360 nm are about 155 ns and 180 ns, respectively, at liquid nitrogen temperature. The former decay time changes its value abruptly near 127 K. This abrupt change of the decay time may be due to the phase transition in pyrene crystals.     

Green oxidation with aqueous hydrogen peroxide

Aqueous H2O2 is an ideal oxidant, when coupled with a tungstate complex and a quaternary ammonium hydrogensulfate as an acidic phase-transfer catalyst. It oxidizes alcohols, olefins, and sulfides under organic solvent- and halide-free conditions in an economically, technically, and environmentally satisfying manner.     

Studies on the constituents of Gardenia species. III. New iridoid glycosides from the leaves of Gardenia jasminoides cv. fortuneana Hara

Two new iridoid glycosides, 7 beta,8 beta-epoxy-8 alpha-dihydrogeniposide (1) and 8-epiapodantheroside (2), were isolated, together with six known (3-8) and three artifact (9-11) iridoids, from the leaves of Gardenia jasminoides cv. fortuneana Hara. Their structures were established based on chemical and spectral data.     

A new norsesquiterpenoid from Russula delica Fr

Russulanorol (1), a new norsesquiterpenoid with a novel carbon skeleton, was isolated from the fruiting bodies of Russula delica FR. (Russulaceae) together with three known sesquiterpenoids. The structure of 1 was elucidated on the basis of spectral data and chemical transformation. Compound 1 is an equilibrium mixture of two stereoisomers (1a, b) on the C-11 acetal carbon.     

First-principles study of the (0 0 1) surface of cubic SrZrO3

Density functional calculations have been used to investigate the (0 0 1) surface of cubic SrZrO₃ with both SrO and ZrO₂ termination. Surface structure and electronic structure have been obtained. The SrO surface is found to be similar to its counterpart in SrTiO₃, while there are marked differences between the ZrO₂ and TiO₂ terminations in SrZrO₃ and SrTiO₃, respectively, concerning surface relaxation and rumpling. For the ZrO₂-terminated surface of SrZrO₃, the covalency of the interaction between the outmost Zr and the O beneath is enhanced as a result of their bond contraction. The band gap reduction and the presence of the surface states are also discussed in relation with the behavior of the electrostatic potential.     

Review Article: Fructooligosaccharides Enzymatic Preparation and Biofunctions

I. INTRODUCTION

Recently the study of oligosaccharides has been extensively pursued in Japan after the findings of the remarkable biofunctions and usefulness of fructooligosac-charides for human health, improving the intestinal microflora and importance in livestock nutrition.     

Boundedness of Product Type Pseudodifferential Operators on Spaces of Besov Type

In this paper we consider pseudodifferential operators associated with symbols satisfying estimates of product type, and give some sufficient conditions for the operators to be bounded on BESOV spaces and on TRIEBEL —LIZORKIN spaces of product type corresponding to the above estimates. In the proof we use the characterization of these spaces by approximation by entire functions.