Synthesis of 5-Thio-D- Galactopyranose

5-Thio-D-galactopyranose has been synthesized from diacetone galactofuranose in nine steps and 13.4% overall yield. The key step involved a successful conversion of furanosyl 5,6-epoxide with an L-altrose configuration into the corresponding 5,6-thiirane D-galactose derivative, which was hydrolyzed to the target compound.     

Effect of pH, temperature and solvent mole ratio on solubility of disodium 5′-guanylate in water + ethanol system

Solubility of disodium 5′-guanylate in water + ethanol binary solvent mixtures was determined by a gravimetric method in the temperature range from 283.15 K to 323.15 K, pH range from 8 to 10 and at different water/ethanol mole ratios. The effects of pH, temperature and water/ethanol mole ratio on the solubility were investigated in detail. The modified Apelblat model and the combined nearly ideal binary solvent (CNIBS)/Redlich-Kister model were selected to correlate the experimental data. The results showed that the experimental data was satisfactorily correlated by the (CNIBS)/Redlich-Kister model, but for the modified Apelblat model, the correlation was not so satisfactory in some cases.     

Poly(p‐phenylene methylene)‐based block copolymers by mechanistic transformation

The synthesis of poly(p‐phenylene methylene) (PPM)‐based block copolymers such as poly(p‐phenylene methylene)‐b‐poly(ε‐caprolactone) and poly(p‐phenylene methylene)‐b‐polytetrahydrofuran by mechanistic transformation was described. First, precursor PPM was synthesized by acid‐catalyzed polymerization of tribenzylborate at 16 °C. Then, this polymer was used as macroinitiators in either ring‐opening polymerization of ε‐caprolactone or cationic ring‐opening polymerization of tetrahydrofuran to yield respective block copolymers. The structures of the prepolymer and block copolymers were characterized by GPC and ¹H NMR investigations. The composition of block copolymers as determined by ¹H NMR and TGA analysis was found to be in very good agreement. The thermal behavior and surface morphology of the copolymers were also investigated, respectively, by differential scanning calorimetry and atomic force microscopy measurements, and the contribution of the major soft segment has been observed. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

New and efficient high Stokes shift fluorescent compounds: unsymmetrically substituted 1,2-bis-(5-phenyloxazol-2-yl)benzenes via microwave-assisted nucleophilic substitution of fluorine

Two new unsymmetric derivatives of 1,2-bis-(5-phenyloxazol-2-yl)benzene (ortho-POPOP) were synthesized via microwave-assisted nucleophilic substitution of fluorine which appears to be significantly more efficient compared with conventional thermal activation. The compounds synthesized are characterized by high fluorescence Stokes shifts (6000-11,000 cm⁻¹) in solvents of various polarity, intermediate-to-high fluorescence quantum yields and lifetimes in the range of several nanoseconds.     

Triphenyl Phosphonium Perchlorate–Catalyzed Imino Diels–Alder Synthesis of Azabicyclo[2.2.2]octan‐5‐ones

Abstract

A facile synthesis of azabicyclo[2.2.2]octan‐5‐ones by triphenyl phosphonium perchlorate–catalyzed imino Diels–Alder reaction of Schiff bases with cyclohex‐2‐enone.     

Global Geometry of 3-Body Motions with Vanishing Angular Momentum Ⅰ

Following Jacobi＇s geometrization of Lagrange＇s least action principle, trajectories of classical mechanics can be characterized as geodesics on the configuration space M with respect to a suitable metric which is the conformal modification of the kinematic metric by the factor （U ＋ h）, where U and h are the potential function and the total energy, respectively. In the special case of 3-body motions with zero angular momentum, the global geometry of such trajectories can be reduced to that of their moduli curves, which record the change of size and shape, in the moduli space of oriented m-triangles, whose kinematic metric is, in fact, a Riemannian cone over the shape space M^＊≌S^2 （1/2）.
In this paper, it is shown that the moduli curve of such a motion is uniquely determined by its shape curve （which only records the change of shape） in the case of h≠0, while in the special case of h = 0 it is uniquely determined up to scaling. Thus, the study of the global geometry of such motions can be further reduced to that of the shape curves, which are time-parametrized curves on the 2-sphere characterized by a third order ODE. Moreover, these curves have two remarkable properties, namely the uniqueness of parametrization and the monotonieity, that constitute a solid foundation for a systematic study of their global geometry and naturally lead to the formulation of some pertinent problems.     

Geometry of 2×2 Hermitian matrices over any division ring

Let D be a division ring with an involution-,H2(D) be the set of 2 × 2 Hermitian matrices over D. Let ad(A,B) = rank(A-B) be the arithmetic distance between A,B ∈ H2(D) . In this paper,the fundamental theorem of the geometry of 2 × 2 Hermitian matrices over D(char(D) = 2) is proved:if  :H2(D) → H2(D) is the adjacency preserving bijective map,then  is of the form (X) = tP XσP +(0) ,where P ∈ GL2(D) ,σ is a quasi-automorphism of D. The quasi-automorphism of D is studied,and further results are obtained.     

Iron Species Present in Fe/ZSM-5 Catalysts – Influence of the Preparation Method

The Fe species present in Fe/ZSM-5 catalysts prepared by ionic exchange in aqueous solution or in the solid state are investigated. The samples were characterized by XRD, EPR, Mössbauer Spectroscopy (MOS-S) and chemical analysis. XRD showed that the peak intensity decreased with the increase in Fe content in the samples. EPR and MOS-S showed that the Fe atoms in all the activated samples appear as Fe⁺³, independently of the method used in the catalyst preparation. The MOS-S data also showed that Fe/ZSM-5, prepared by ion exchange in the solid state presented lower hematite content and more Fe species in charge-compensation sites, the responsible for the catalytic activity, as confirmed by the behavior in the propane oxidation.