Unexpected reaction of a dimethylzinc-generated THF radical with aldehydes

A dimethylzinc-air-generated THF radical reacted with aldehydes at the β-position of an α-oxygenated THF.     

Additives for the separation of cesium from a strongly nitric acid medium by insoluble ferrocyanide sorbents

In the presence of trace amounts of hydrazinium or amidosulfate ion, sufficiently high values were observed for the distribution coefficients of cesium on several insoluble ferrocyanide sorbents in a concentrated solution of nitric acid, in contrast to considerably lower values in their absence. The results indicate an inhibitory action of the above agents on the oxidation of ferrocyanide to ferricyanide with nitric acid.     

Spontaneous two-photon emission from a single quantum dot

Spontaneous two-photon emission from a solid-state single quantum emitter is observed. We investigated photoluminescence from the neutral biexciton in a single semiconductor quantum dot coupled with a high Q photonic crystal nanocavity. When the cavity is resonant to the half energy of the biexciton, the strong vacuum field in the cavity inspires the biexciton to simultaneously emit two photons into the mode, resulting in clear emission enhancement of the mode. Meanwhile, the suppression of other single photon emission from the biexciton was observed, as the two-photon emission process becomes faster than the others at the resonance.     

Basic sites on periodic mesoporous organosilicas investigated by XPS and in situ FTIR of adsorbed pyrrole

Oxygen sites in ethane-bridged and phenylene-bridged PMOs prepared using neutral templates in acidic conditions are characterized by means of XPS and FTIR spectroscopy of adsorbed pyrrole. Their electron donor ability is observed to be stronger than that of oxygens in pure amorphous silica of MCM-41 type and comparable to that reported for oxygen atoms in some alkali metal exchange zeolites. For pyrrole adsorbed on PMOs double interactions most probably occur, involving both silanols and electron donor sites at the surface. In the case of phenylene-bridged PMO preferential electron donor sites for interaction with pyrrole N-H group are aromatic rings rather than oxygens, as previously observed for adsorbed iodine.     

PERFORMANCE OF SHORTER PERIODICAL DOMAIN OF NEMATIC LIQUID CRYSTAL INDUCED BY ELASTIC WAVE PROPAGATION

Abstract

The light diffraction properties of a shorter periodical domain, which is caused by an elastic wave propagating along one of two glass plates composing a liquid crystal cell, are described. The shorter periodical domain is controllable for the application of an electric field to the liquid crystal cell. The response time of the disappearance of the shorter periodical domain decreases with increasing the applied voltage. On the other hand, the response time of the domain formation is independent of the applied voltage. These response times agree quantitatively with those of the birefringence electrooptic effect. The domain disappearance by applying the voltage to the liquid crystal indicates the Freedericksz transition.     

Porphyrin derivatives act as vinylene monomers in TEMPO‐mediated radical copolymerization with styrene

In this article, we offer clear evidence for the radical copolymerizability of porphyrin rings in 2,2,6,6‐tetramethyl‐1‐piperidinyloxy (TEMPO)‐mediated radical copolymerizations with styrene. The radical copolymerizations of styrene with 5,10,15,20‐tetrakis(pentafluorophenyl)porphyrin (H₂TFPP) was conducted using 1‐phenyl‐1‐(2,2,6,6‐tetramethyl‐1‐piperidinyloxy)ethane as an initiator. The refractive index (RI) traces for the size‐exclusion chromatography of the resulting copolymers were unimodal with narrow molecular weight distributions. The RI traces shifted toward higher molecular weight regions as the polymerization progressed, and the number‐average molecular weights were close to those calculated on the basis of the feed compositions and monomer conversions. These features were in good agreement with a TEMPO‐mediated mechanism. The traces recorded by the ultraviolet‐visible (UV‐vis) detector (430 nm) were identical to those obtained by the RI detector, indicating a statistical copolymerization of styrene with H₂TFPP. This also indicated that H₂TFPP acted as a monomer and not as a terminator or a chain‐transfer agent under the conditions used. A benzyl radical addition to H₂TFPP was conducted as a model reaction for the copolymerization using tributyltin hydride as a chain‐transfer agent, affording a reduced porphyrin, 2‐benzyl‐5,10,15,20‐tetrakis(pentafluorophenyl)chlorin 1 , via radical addition to the β‐pyrrole position. The UV‐vis spectrum of 1 was fairly similar to that of poly(styrene‐co‐H₂TFPP), indicating that H₂TFPP polymerized at its β‐pyrrole position in the TEMPO‐mediated radical polymerization. TEMPO‐mediated radical copolymerizations of styrene with several porphyrin derivatives were also demonstrated. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Red Yeast Rice Fermentation by Selected Monascus sp. with Deep-Red Color, Lovastatin Production but No Citrinin, and Effect of Temperature-Shift Cultivation on Lovastatin Production

Monascus pilosus NBRC4520 was selected for functional fermented food inoculation for its high lovastatin and low citrinin production with a deep-red color. For koji (mold rice) with high lovastatin production, separation of the growth phase and lovastatin production phase by shifting the temperature from 30 to 23 °C increased lovastatin production by nearly 20 times compared to temperature-constant cultivation. In addition, citrinin was not produced even in the lovastatin production phase, although the pigment was increased. With temperature-shift cultivation, 225 μg lovastatin/g dry koji was produced in 14 days without citrinin.     

Characterization of frequency-tripled nanosecond pulsed Ti:sapphire laser injection seeded by a frequency-scanning cw Ti:sapphire laser by use of optogalvanic spectroscopy of silicon atoms

The performance of a narrow-linewidth nanosecond pulsed deep-UV coherent light source consisting of a frequency-tripled nanosecond pulsed Ti:sapphire laser injection seeded by a frequency-scanning cw Ti:sapphire laser has been characterized by using optogalvanic spectroscopy of silicon atoms as a diagnostic. The envelope of the optogalvanic spectrum indicates the pure Doppler broadening of silicon atoms, which was estimated to be as broad as 4 GHz, without the broadening effect from the laser linewidth itself.     

Structure-driven nonlinear instability of double tearing modes and the abrupt growth after long-time-scale evolution

The new nonlinear destabilization process is found in the nonlinear phase of the double tearing mode (DTM). This process causes the abrupt growth of DTM and subsequent collapse after long-time-scale evolution in the Rutherford-type regime. The nonlinear growth of the DTM is triggered when the triangular deformation of magnetic islands with sharp current point at the X point exceeds a certain value. Hence, the mode can be called the structure-driven one. Decreasing the resistivity increases the sharpness of the triangularity and the spontaneous growth rate in the abrupt-growth phase is almost independent of the resistivity.