Regression-based model of skin diffuse reflectance for skin color analysis

A simple regression-based model of skin diffuse reflectance is developed based on reflectance samples calculated by Monte Carlo simulation of light transport in a two-layered skin model. This reflectance model includes the values of spectral reflectance in the visible spectra for Japanese women. The modified Lambert Beer law holds in the proposed model with a modified mean free path length in non-linear density space. The averaged RMS and maximum errors of the proposed model were 1.1 and 3.1%, respectively, in the above range.     

Observables and quark confinement in the covariant canonical formalism of Yang-Mills theory

A concise criterion for observables in Yang-Mills theory is presented in the framework of covariant canonical field theory. As an example, the symmetric energy-momentum tensor θ_øν is proved to be an observable and its physically meaningful form is clarified. The validity of the “Maxwell-type” equation of motion is established in the physical subspace $\text{V}$_phys defined by the subsidiary condition $\text{Q}{}_{\mathrm{<mtext>B</mtext>}}\text{?}\text{phys}\text{〉 = 0}$ (Q_B: BRS charge). Its meaning and consequences are discussed in connection with the notion of observables: especially, all (quasi-) local observables in QCD are shown to be colour singlets and this fact paves the way to quark confinement.     

The synthesis of 2-ethoxy-6,11-dimethyl-7,9-bisdehydroaza[14]annulene and its benzannelated derivatives

Title azaannulenes were synthesized starting from annulenones, and the ¹H-NMR spectra are discussed in connection with tropicity of these annulenes.     

Photoreduction behavior of cytochrome c by zinc porphyrin in lipid media

To elucidate the role of cardiolipin (CL) on redox behavior of cytochrome c (cyt c (III)), the photoreduction of cyt c using the photosensitization of zinc tetraphenylporphyrin in presence of triethanolamine (TEOA) as a sacrificial electron-donating reagent in various lipid media were studied. The initial rate of cyt c (III) photoreduction in various lipid, CL, l-alpha-phosphatidic acid (PA), dimethyldipalmitoylammonium bromide (DMPA) and Triton X-100 media were 1.0, 0.73, 0.80 and 0.67 micromol dm-3 min-1, respectively. The cyt c (III) photoreduction rate slightly increased by the addition of CL.     

Asymmetric synthesis of β-lactams. I. The reaction of dimethylketene silyl acetal with (S)-alkylidene(1-arylethyl)amines promoted by titanium tetrachloride

Asymmetric synthesis of β-lactams by means of the reaction of dimethylketene silyl acetal with (S)-alkylidene(1-arylethyl)amines in the presence of titanium tetrachloride was studied. The extent of the asymmetric induction was in the range of 44–78% (diastereomeric purity 72–89%) and the (S)-configuration was turned to be preferentially induced at the ⁴C position of the resulting β-lactams.     

Redox-Induced Modulation of Exchange Interaction in a High-Spin Ground-State Diradical/Triradical System

A triplet ground-state diradical molecule, bis(nitronyl nitroxide)-substituted diphenyldihydrophenazine ( 1 ^..), that can be converted into a one-electron oxidized species, 1 ^{… +} , in the quartet ground state has been developed. Surprisingly, these species, 1 ^.. and 1 ^{… +} , can be used under ambient conditions because they are reasonably stable under aerobic conditions, even in solution. The temperature-dependent magnetic susceptibilities reveal that 1 ^.. and 1 ^{… +} are in the triplet state, with a weak exchange interaction (J₁/k_B = +3.1 K) and quartet ground state with a strong exchange interaction (J₂/k_B = +160 K), respectively. The interconversion between the neutral and one-electron oxidized species can be realized through electrochemical reactions. Significantly different absorption bands in the near-IR region newly appeared in the electronic spectra acquired during electrochemical oxidation/reduction.     

Very strong hydrogen bonds in a bent chain structure of fluorohydrogenate anions in liquid Cs(FH)2.3F

The structure of liquid Cs(FH)(2.3)F was revealed using a combination of high-energy x-ray and neutron diffraction measurements. We found that the strongest intermolecular H-F hydrogen bonds at an average distance of 1.36 A are accompanied by the formation of a high degree of bending of the oligomer chain in the melt, with [angle]FHF=150 degrees . A reverse Monte Carlo simulation showed that the average number of atoms per chain is 4.4. A detailed chain analysis of the atomic configuration revealed that (FH)(2)F(-) oligomer chains are the major entities in the liquid, and asymmetrical FHF(-) are formed owing to the strong H-F hydrogen bonds. The results suggest that an average of one or two HF molecules bond to each of the 11 fluorine atoms surrounding a cesium ion.