Tin-catalyzed conversion of trioses to alkyl lactates in alcohol solution

Tin chlorides, SnCl2 and SnCl4.5H2O are excellent catalysts for the reactions of trioses, dihydroxyacetone and glyceraldehyde with alcohols (MeOH, EtOH and nBuOH) to give alkyl lactates, whose reaction mechanism involves the intermediary formation of pyruvic aldehyde followed by its esterification, which is distinctively promoted by tin halides.     

The N—H stretching vibrations and conformations of trialkylthioureas

The ν(N-H) vibrations of trialkylthioureas observed in the dilute solutions are interpreted in relation to the trans—out isomerism. Occurrence of the out form is discussed from the point of view of steric hindrance. The two forms are characterized by the behavior of ν(N—H) vibrations at several concentrations. Solid DiPTUtB and DcHTUtB exhibited one sharp band at the same position as the ν(N—H) band in solution. This indicates that they are in the out form in the solid state as well as in solution.     

A remark on the transformation formula of theta functions associated to positive definite quadratic forms

Let L be a positive Z-lattice with level N = cd, (c, d) = 1. Then the Fourier expansion at cusp $\text{1}\text{d}$ of the theta function associated to L is a theta function associated to L₁, where a lattice L₁ is defined by Z_pL₁ = Z_pL for $\text{p?c}$, Z_pL₁ = the dual of Z_pL for p | c.     

Microwave l-type resonance transitions of the v6 = 1 state in CHF3 and CDF3: Accidental degeneracy and molecular structure

Observations of the direct l-type resonance transitions in the microwave spectrum of the v₆ = 1 state of CHF₃ and CDF₃ have been extended to J = 37. Accidental degeneracies were found between J = 34, $\text{K}\text{= 3}\text{and}\text{0}$ in both molecules enabling the C rotational constants of CHF₃ and CDF₃ to be determined, using 118 observed frequencies for CHF₃ and 104 for CDF₃. After suitable correction the B and C rotational constants were used to determine the r₀, r₂, and r_e structures for CHF₃ and CDF₃.The equilibrium structure was determined to be $\text{CH}\text{= 1.091 ± 0.014}\text{A}\text{?}$, $\text{CF}\text{= 1.3284 ± 0.0031}\text{A}\text{?}$ and ∠FCF = 108.58 ± 0.34°.     

Bioorganic studies on plant movement, from natural products to its receptor

The chemical aspects of the circadian leaf movement known as "nyctinasty" are discussed in this paper. Each of the nyctinastic plants of five different genera so far examined contained a pair of factors, one of which induced leaf closure and another induced leaf opening. The relative contents of the closing and opening factors changed correlating with the nyctinastic leaf movement. The use of fluorescence-labeled and photoaffinity-labeled factors revealed that the factors bind to specific cells, the motor cells, present in the pulvini, and that the membrane fraction of the motor cells contained two proteins of 210 and 180 kDa, which can bind to the factors.     

Cell adhesion molecules nectins and associating proteins: Implications for physiology and pathology

Nectins have recently been identified as new cell adhesion molecules (CAMs) consisting of four members. They show immunoglobulin-like structures and exclusively localize at adherens junctions (AJs) between two neighboring cells. During the formation of cell–cell junctions, nectins function in cooperation with or independently of cadherins, major CAMs at AJs. Similar to cadherins, which are linked to the actin cytoskeleton by binding to catenins, nectins also bind to afadin through their C-terminal region and are linked to the actin cytoskeleton. In addition to nectins, there are nectin-like molecules (Necls), which resemble nectins in their structures and consist of five members. Nectins and Necls are involved in the formation of various kinds of cell–cell adhesion, and also play key roles in diverse cellular functions including cell movement, proliferation, survival, and differentiation. Thus, nectins and Necls are crucial for physiology and pathology of multicellular organisms.     

A Bayesian approach to pricing longevity risk based on risk-neutral predictive distributions

We present a Bayesian approach to pricing longevity risk under the framework of the Lee-Carter methodology. Specifically, we propose a Bayesian method for pricing the survivor bond and the related survivor swap designed by Denuit et al. (2007). Our method is based on the risk neutralization of the predictive distribution of future survival rates using the entropy maximization principle discussed by Stutzer (1996). The method is illustrated by applying it to Japanese mortality rates.     

Sorption of water vapor into polyelectrolyte complex of poly(styrenesulfonic acid)/poly(4-vinyl-N-ethylpyridinium bromide)

Successive differential and integral sorptions of water vapor into the polyelectrolyte complex of poly (sty renesulfonic acid) / poly(4-vinyl-N-ethylpyridinum bromide) have been measured; films of stoichiometric (1/1 molar ratio) and nonstoichiometric (2/1 molar ratio) complex were employed in the experiments. Sorption isotherms have been also determined by using the values obtained from integral sorption experiments. The sorption data have suggested the following. (i) The rearrangement of polymer chains plays a relatively unimportant role in sorption of water. (ii) The relaxation motion of network chains is suppressed. (iii) The change of morphological structure caused by vapor sorption is obscure. (iv) The ionic character of the 1/1 complex is higher than that of 2/1 complex. (v) A small amount of water can be dispersed on specific polymer sites, but the sorption of a large amount of water is accompanied by an expansion of network structure. Points (i)-(v) have been consistently interpreted on the basis of the network structure and ionic character of this complex.     

Microstructure of Milled Mesophase Pitch-Based Carbon Fibers as an Anode Material for Li-ion Batteries

Abstract

The microstructure of milled mesophase pitch-based carbon fibers (mMPCFs) that have been developed as an anode material for Li ion batteries have been studied as a function of heat treatment temperature (HTT), by SEM, X-ray diffraction, and Raman spectroscopy. And the results obtained are compared with those by X-ray diffraction (XRD) and SEM observations, for the characterization of specific structural features of mMPCFs as a promising anode material.