Electroprotic reactions

Reactions involving the coupled transfer of electrons and protons are called electroprotic reactions. In this article we briefly describe some of our experiences with electroprotic reaction as a tool for executing interesting chemical transformations.     

Pattern formation of zinc nanoparticles in silica film by electrodeposition

Zinc nanoparticles were grown within gel-derived silica films by applying a direct current voltage. Pattern formation of metallic Zn was studied as a function of applied voltage and metal-silica ratio. Average particle size varied from 5.2 to 20.2 nm by changing the applied voltage and silica concentration. It was found that the transition from fractal to dendritic morphology was possible due to crystalline anisotropy. From high-resolution transmission electron microscopy images and X-ray diffraction pattern a possible model is proposed to explain this observation.     

Dinuclear copper (II) and nickel (II) systems with planar M2N2O2 bridge

The tridentate ligand systemb (abbreviated as inkR₂) readily yield copper (II) and nickel (II) species of the formula M₂ (inkR₂)₂(CLO₄)₂. 2xH₂O (x=0–1). Dinuclear formulation is based on variable temperature magnetic susceptibility and conductivity data and on the known structure of some related systems. The Cu₂ (inkR₂) ₂ ²⁺ species are strongly antiferromagnetic (?2J=600–800 cm^?1) while the Ni₂(inkR₂) ₂ ²⁺ species are diamagnetic. The major coordination sphere is planar around each metal (II). The metal ions in a dimer are linked by planar M₂N₂O₂ bridge. The copper (II) and nickel (II) species freely form solid solutions. In these statistical scrambling of copper and nickel occur among the metal ion sites of the dimeric structure. Powder epr spectra of such mixed crystals are indicative of axial geometry around copper (II) ion.     

Synthesis and thermal behavior of chiral oligomers derived from cholesterol

Synthesis and thermal properties of a series of Schiff base oligomers derived from naturally occurring cholesterol are described. In particular, four of them show smectic A and/or chiral nematic phase/s or an unknown mesophase, while the other is non-mesomorphic. Molecular packing in the SmA phase has been determined by the HRXRD experiment.     

Solvable lattice gas models of random heteropolymers at finite density: II. Dynamics and transitions to compact states

The European Physical Journal E - In this paper we analyse both the dynamics and the high density physics of the infinite dimensional lattice gas model for random heteropolymers recently introduced...     

Reagent Selector: using Synthon Analysis to visualize reagent properties and assist in combinatorial library design

Reagent Selector is an intranet-based tool that aids in the selection of reagents for use in combinatorial library construction. The user selects an appropriate reagent group as a query, for example, primary amines, and further refines it on the basis of various physicochemical properties, resulting in a list of potential reagents. The results of this selection process are, in turn, converted into synthons: the fragments or R-groups that are to be incorporated into the combinatorial library. The Synthon Analysis interface graphically depicts the chemical properties for each synthon as a function of the topological bond distance from the scaffold attachment point. Displayed in this fashion, the user is able to visualize the property space for the universe of synthons as well as that of the synthons selected. Ultimately, the reagent list that embodies the selected synthons is made available to the user for reagent procurement. Application of the approach to a sample reagent list for a G-protein coupled receptor targeted library is described.     

Palladium-mediated reductive Mizoroki-Heck cyclization strategy for the regioselective formation of dibenzoazocinone framework

The synthesis of dibenzoazocine framework through palladium-mediated reductive Mizoroki-Heck cyclization has been described. The procedure is simple, straightforward, and regioselective.