Charge screening in a plasma with an external ionization source

An asymptotic theory for the screening of the electric field of a dust particle or a spherical probe in a plasma with an external steady and/or internal (proportional to the electron density) gas ionization source has been developed for the first time. It has been established that the screening of the charge of a spherical body adsorbing the charge of the incident plasma particles is described by a superposition of two exponentials with different screening constants. The two exponentials are retained even in the absence of nonequilibrium fluxes on the macroparticle and only in the special case of an isothermal plasma does the screening become Debye one. The screening length is determined by the ratio of the electron-ion, β_ei, and Langevin, β_L = 4πeμ_i (where μ_i is the ion mobility), recombination coefficients. If β_L ? β_ei, then it is much larger than the electron Debye length. The ions in an isothermal plasma have been found to give the same contribution to the screening as the electrons if the electron-ion recombination coefficient exceeds the Langevin ion recombination coefficient by a factor of 2 or more, β_ei ≥ 2β_L. The Vlasov equation is used to analyze the asymptotic behavior of the macroparticle potential in a collisionless plasma.     

Synthesis and Biological Studies of O3-Aryl Galactosides as Galectin Inhibitors

β-Galactose derivatives have recently been reported to selectively inhibit galectin-3, and a library of O3-arylated galactosides with varying substitution patterns was designed to study such inhibitions further. The O3-arylated galactosides were synthesized using diaryliodonium salts under mild and transition metal free conditions, providing the target products in moderate to good yields. An O3-trifluoroethylated galactoside was also synthesized using iodonium salt chemistry. Azido-substituted products were subsequently transformed into the corresponding triazoles. After deprotection, a selection of galactoside derivatives were evaluated for inhibitory potencies against galectins-1, 3, 4 N (N-terminal domain), 4 C (C-terminal domain), 7, 8 N, 8 C, 9 N, and 9 C and one compound with promising affinity and selectivity for both the N- and C-terminal domain of galectin-9 was discovered.     

The rate of chloroacetic acid alkaline hydrolysis: Medium effect

Rate constant of chloroacetic acid alkaline hydrolysis in the mixed aqueous-organic solvents depends on the organic co-solvent nucleophilic solvation; however, the effect of the medium polarity on the rate constant is not clear. The rate constant can be reasonably estimated with a multi-parameter equation accounting for the organic co-solvent basicity as well as its density of cohesion energy and molar volume.     

Thermal studies of furosemide–caffeine binary system that forms a cocrystal

Thermal techniques, differential scanning calorimetry (DSC), and hot stage microscopy (HSM) have been used to study the interactions between furosemide and caffeine that are known to form a 1:1 cocrystal. This system has been used as an example to study the probable mechanism of cocrystal formation when the individual components, which are polymorphic, are heated. The study indicates that the phase transition of the low temperature stable polymorph of furosemide initiates cocrystal formation. This result suggests increased mass transfer rate can trigger cocrystal formation. The binary phase diagram (composition–temperature plots) of furosemide–cocrystal–caffeine system was determined from the DSC curves. The results imply that the cocrystal forms eutectic with caffeine but not with furosemide. This study has thus exemplified the use of DSC in understanding binary phase system where the two components form a cocrystal.     

Theoretical modeling of Cu(II), Sr(II), Gd(III), U(VI) sorption from nuclear effluent on PHA resin with experimental validation

Journal of Radioanalytical and Nuclear Chemistry - The sorption capacity of an in–house synthesized novel resin Polyhydraxamic acid(PHA) towards Cu(II), Sr(II), Gd(III), U(VI) ions was...     

α-Amidoaldehydes as Substrates in Rhodium-Catalyzed Intermolecular Alkyne Hydroacylation: The Synthesis of α-Amidoketones

We show that readily available α-amidoaldehydes are effective substrates for intermolecular Rh-catalyzed alkyne hydroacylation reactions. The catalyst [Rh(dppe)(C₆H₅F)][BAr^F₄] provides good reactivity, and allows a broad range of aldehydes and alkynes to be used as substrates, delivering α-amidoketone products. High yields and high levels of regioselectivity are achieved. The use of α-amidoaldehydes as substrates establishes that 1,4-dicarbonyl motifs can be used as controlling groups in Rh-catalyzed hydroacylation reactions.