Discrete Dynamical Systems with W(A (1) m−1 × A (1) n−1) Symmetry

We give a birational realization of affine Weyl group of type A ⁽¹⁾ _m–1 × A ⁽¹⁾ _n–1. We apply this representation to construct some discrete integrable systems and discrete Painlevé equations. Our construction has a combinatorial counterpart through the ultra-discretization procedure.     

Development of micromarkers with various photoluminescence colors as tracers for shadowing pursuits.

Micromarkers with five photoluminescence colors were developed as tracers for shadowing pursuits. The markers are colorless powders with particle diameters of several tens to several hundreds of micrometers, prepared using a cryogenic sample crusher. They were visualized using red, green, yellow, magenta or cyan photoluminescence under ultraviolet light at approximately 365 nm. The markers were composed of photoluminescent compounds dispersed in polyvinyl butyral. The photoluminescent compounds in the polyvinyl butyral were stable under ambient conditions for more than one year after application. The compounds with the red, green, yellow, magenta and cyan photoluminescence contained a europium (Eu(3+)) complex, a terbium (Tb(3+)) complex, a mixture of Tb(3+) and Eu(3+) complexes, a mixture of Eu(3+) complex and o-coumaric acid, and a mixture of Tb(3+) complex and 7-hydroxycoumarin along with a few drops of a sodium bicarbonate aqueous solution, respectively. Neodymium (Nd(3+)) and ytterbium (Yb(3+)) complexes with photoluminescence in the near-IR wavelength region can also be added to these visible photoluminescent compounds as secret markers for discrimination. The markers were non-destructively identified using a microscopic FT-IR spectrometer and a microscopic spectrometer equipped with a fluorescence detector.     

A three carbon homologation by the ring-opening of β-propiolactones with diorganocuprates

Various organocuprates react with β-propiolactones to give β-substituted propionic acids in high yields.     

Mechanism of infrared stimulation and quenching in ZnS: Cu,Al Phosphors

To investigate the mechanism of the stimulation and quenching of the green luminescence in ZnS: Cu, Al phosphors by infrared (IR) light of 0.7–1.5 μm, stimulation and quenching spectra, IR effects on time-resolved emission spectra, and IR-induced photoconductivity are measured at 4.2 K, 77 K, and room temperature. Both the stimulation and quenching are caused by the IR transitions ascribed to excited copper acceptors. It is concluded that the stimulation is induced by the process in which holes produced by IR light migrate among copper acceptors, so that the statistical distribution of the intrapair separations of excited copper-aluminum pairs are changed to shorter distances. It is found that at low temperatures the holes migrate from one copper acceptor to another without being thermally released to the valence band. It is confirmed that the quenching is caused by the recombination of holes released to the valence band with electrons in the conduction band via some kind of nonradiative recombination centers.     

Fluorescent products of the reaction of mono-substituted guanidino compounds with benzoin-dimethylformamide

The fluorescent products formed from methylguanidine or phenylguanidine and benzoin in the presence of dimethylformamide are shown to be the corresponding 2-substituted amino-4, 5-diphenylimidazoles. They fluoresce most intensely at pH 9–10 and the fluorescence is stabilized by β-mercaptoethanol.     

Efficient synthesis of optically active atropisomeric anilides through catalytic asymmetric N-arylation reaction

In the presence of (R)-DTBM-SEGPHOS-Pd(OAc)2 catalyst, N-arylation of ortho-tert-butyl-NH-anilides with 4-nitroiodobenzene proceeds with high enantioselectivity (89-95% ee) to give optically active atropisomeric anilides possessing N-C chiral axis. Furthermore, the intramolecular version of the present catalytic asymmetric N-arylation gave atropisomeric lactams with high optical purity (94-96% ee).