Mn doping concentration dependent p–d hybridization in Ga1−xMnxN

The 3d electronic states of transition-metal Mn dopants in ${\mathrm{Ga}}_{1?x}{\mathrm{Mn}}_{x}N$ have been investigated by Mn $L$-edge X-ray absorption spectroscopy (XAS) measurements. Through the XAS analysis, the valence of the Mn ions is determined. With the increase of doping concentration, the integrated intensities of $L_{2,3}$ vary not monotonously, but increase first and then decrease. The relationship between the Mn doping concentration and the degree of p–d hybridization is discussed.     

Demonstration of diamond field effect transistors by AlN/diamond heterostructure

This is the first report on an AlN/diamond heterojunction field effect transistor (HFET). The AlN epilayer is grown on oxygen‐terminated (111) diamond substrates using metalorganic vapor phase epitaxy at a temperature as high as 1240 °C. The transistor and gate capacitance–voltage characteristics indicate that the HFET behaves as a p‐channel FET with a normally‐on depletion mode. The HFET channel is located at the AlN/diamond interface, and holes are accumulated in diamond close to the interface. The development of the AlN/diamond HFET creates a new possibility for diamond‐based power electronics. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Fluorogenic Probe Using a Mislow–Evans Rearrangement for Real‐Time Imaging of Hydrogen Peroxide

Hydrogen peroxide (H₂O₂) mediates the biology of wound healing, apoptosis, inflammation, etc. H₂O₂ has been fluorometrically imaged with protein‐ or small‐molecule‐based probes. However, only protein‐based probes have afforded temporal insights within seconds. Small‐molecule‐based electrophilic probes for H₂O₂ require many minutes for a sufficient response in biological systems. Here, we report a fluorogenic probe that selectively undergoes a [2,3]‐sigmatropic rearrangement (seleno‐Mislow‐Evans rearrangement) with H₂O₂, followed by acetal hydrolysis, to produce a green fluorescent molecule in seconds. Unlike other electrophilic probes, the current probe acts as a nucleophile. The fast kinetics enabled real‐time imaging of H₂O₂ produced in endothelial cells in 8 seconds (much earlier than previously shown) and H₂O₂ in a zebrafish wound healing model. This work may provide a platform for endogenous H₂O₂ detection in real time with chemical probes.     

In-situ RHEED study on the effect of light irradiation on Ge/Si heteroepitaxial growth by GeH4 source MBE

Effects of light irradiation on growth processes in the initial stage of growth of Ge films on (100)Si substrates by gas source molecular beam epitaxy using GeH₄ have been investigated by in-situ RHEED observations. It has been found that the growth rate is enhanced by an Ar⁺ ion laser and a D₂ lamp irradiation, and, moreover, that the growth process sequence of the Ge films irradiated by the Ar⁺ laser and D₂ lamp is the same as that without irradiation. The irradiation effect on the photolysis of GeH₄ gas has been examined by mass spectroscopy. The increase of the growth rate is due to the photolysis of GeH₄ and the excitation of substrate surfaces by vacuum-ultraviolet light in the D₂ lamp irradiation, and is due to only the excitation of substrate surfaces in the Ar⁺ laser irradiation.     

Surface‐Modifiable Free‐Floating Films Formed by Multiway Connection of Collagen‐Like Triple‐Helical Peptides

Square‐millimeter‐sized free‐floating translucent films are formed in physiological buffer by multiway connections between biotinylated collagen‐like triple‐helical peptides and avidin. Although the compositions of the films are almost constant, regardless of the ratios of the components loaded, their thicknesses can be controlled by the concentrations of the components. The film surfaces can be further modified by taking advantage of exposed biotin (or avidin) functionalities. The self‐assembled films could serve as novel materials in biomedical and biosensing applications.     

Synthesis and thermal properties of side chain-type liquid crystalline polyurethanes

Abstract

The synthesis of side chain-type polyurethanes is described. Their thermal properties were investigated by differential scanning calorimetry and polarizing microscopy and are discussed in terms of the dependence of the polymer backbone on temperature as shown by FT-infrared spectroscopy. The hydrogen bonding which arises from the rather flexible polymer backbone plays a more important role in determining the thermal stability than does the rigid polymer backbone.     

The structure of neocarzinostatin chromophore possessing a novel bicyclo-[7,3,0]dodecadiyne system

The structure of the chromophore of an antitumor antibiotic neocarzinostatin has been elucidated as a bicycro[7,3,0]dodecadiyne system having naphthalenecarboxylic acid, aminosugar and ethylene carbonate units.     

Synthesis and thermal properties of side chain-type liquid crystalline polyurethanes

The synthesis of side chain-type polyurethanes is described. Their thermal properties were investigated by differential scanning calorimetry and polarizing microscopy and are discussed in terms of the dependence of the polymer backbone on temperature as shown by FT-infrared spectroscopy. The hydrogen bonding which arises from the rather flexible polymer backbone plays a more important role in determining the thermal stability than does the rigid polymer backbone.