One-pot synthesis of 1-substituted-5-alkylselanyl-1H-tetrazoles from isoselenocyanates: unexpected formation of N-alkyl-N-arylcyanamides and (Z)-Se-alkyl-N-cyano-N,N′-diarylisoselenoureas

1-Substituted-5-alkylsulfanyl-1H-tetrazoles are well known class of organic substances with various applications in medicinal chemistry or photographic industry. Their selenium analogues, 1-substituted-5-alkylselanyl-1H-tetrazoles are, however, much less explored because of the lack of suitable methods for their preparation. In this work we investigated the synthesis of 1-alkyl/aryl-5-alkylselanyl-1H-tetrazoles from synthetically available alkyl/arylisoselenocyanates. One-pot reactions of arylisoselenocyanates with sodium azide and alkylating agent led to the target 5-alkylselanyl-1-aryl-1H-tetrazoles but also to interesting side products, namely N-alkyl-N-arylcyanamides and (Z)-Se-alkyl-N-cyano-N,N′-diarylisoselenoureas. Nevertheless, when alkylisoselenocyanates were utilized as the substrates, the reactions led exclusively to the formation of 1-alkyl-5-alkylselanyl-1H-tetrazoles in good yields. This simple one-pot procedure brings new possibilities for the preparation of variously substituted selenium compounds. It also opens the way to further investigations of selenium isosteres of the widely utilized 5-thiotetrazole moiety in biomedical applications.     

Physicochemical and adsorption properties of hypercross‐linked polystyrene with ultimate cross‐linking density

The paper describes unexpected properties of hypercross‐linked polystyrenes with ultimate cross‐linking degrees of 300, 400, and 500%, where three, four, or five methylene links, respectively, could bind each polystyrene phenyl ring to its spacious neighbors. The polymers exhibit a strong electron spin resonance signal, unusual spectra in IR, UV, and visible ranges, and they are not typical dielectrics. The nonfunctionalized hypercross‐linked polymers absorb significant amounts of inorganic acids, salts, and bases due to interactions of protons or other cations with electron‐donating fragments of the aromatic network with the high extent of mutual connectivity and also due to dispersion interactions of anions with the polymer matrix.     

Molecular mobility and transport in polymer membranes and polyelectrolyte multilayers

Polyelectrolyte multilayers prepared by the layer-by-layer technique provide an efficient way to generate planar structures of tailored surface charge and hydrophobicity, which are used as membranes for pervaporation. The use of polyelectrolyte multilayers to form the membrane permits tailoring the surface charge of the membrane and, thus, selectivity; at the same time, it reduces fouling of the membrane by adsorption of organic matter. Pulsed field gradient (PFG) nuclear magnetic resonance has been used to investigate the diffusion of probe molecules into polymer systems. Evaluation of the apparent diffusion coefficient in porous poly(amide) results in a pore size of 4 microm, as found in electron micrographs. For the pore size obtained for polyelectrolyte multilayers, no equivalent pores could be found in microscopy. Propagators for the diffusion of propanol and propanol-water mixture into multilayers reveal that there might be selective interaction of probe molecules with the polyelectrolyte system.     

The two-step exponential decay reaction network: analysis of the solutions and relation to epidemiological SIR models with logistic and Gompertz type infection contact patterns

Journal of Mathematical Chemistry - We mathematically analyze the solutions to the dynamical system induced by the two-step exponential (growth-)decay (2SED) reaction network involving three...     

Optical and electrical properties of GaN: Si-based microstructures with a wide range of doping levels

The optical and electrical properties of silicon-doped epitaxial gallium nitride layers grown on sapphire have been studied. The studies have been performed over a wide range of silicon concentrations on each side of the Mott transition. The critical concentrations of Si atoms corresponding to the formation of an impurity band in gallium nitride (～2.5 × 10¹⁸ cm^?3) and to the overlap of the impurity band with the conduction band (～2 × 10¹⁹ cm^?3) have been refined. The maximum of the photoluminescence spectrum shifts nonmonotonically with increasing doping level. This shift is determined by two factors: (1) an increase in the exchange interaction leading to a decrease in the energy gap width and (2) a change in the radiation mechanism as the donor concentration increases. The temperature dependence of the exciton luminescence with participating optical phonons has been studied. The energies of phonon-plasmon modes in GaN: Si layers with different silicon concentrations have been measured using Raman spectroscopy.     

Preparation and Crystal Structure of a New Uranyl Sulfate Templated by a Bis-isothiouronium Cation

Crystals of a new uranyl sulfate (C₂N₄H₈S₂)[UO₂(SO₄)₂] · 0.3H₂O ( 1 ) templated by a relatively rare bis-isothiouronium cation, were formed upon evaporation of aqueous solutions containing uranyl acetate, thiourea, and excess sulfuric acid. The new compound is orthorhombic, P2₁2₁2₁, a = 6.928(2) Å, b = 13.398(3) Å, c = 15.225(3) Å, Z = 2. Its crystal structure is comprised of [UO₂(SO₄)₂] moieties linked by hydrogen bonds formed between the template cations and terminal oxygen atoms of the sulfate tetrahedra. The C₂N₄H₈S₂²⁺ template is most likely formed in situ during a redox reaction between uranyl cation and thiourea in a strongly acidic medium, with UO₂²⁺ partially reduced to U⁴⁺.     

Leaching of Impurities from Poor Intermediate Products of Refining Production in Autoclave Conditions

Russian Journal of Applied Chemistry - At elevated temperatures (130 and 180°C) in hydrothermal autoclave conditions, the possibility of deep extraction of noble metals from poor intermediate...     

Effects of Dry-Jet Wet Spinning Parameters on Properties of Polysulfone Hollow Fiber Membranes

Russian Journal of Applied Chemistry - The influence of parameters of the dry-jet wet spinning process was studied on properties of porous polysulfone hollow fiber membranes. The air gap distance,...     

Polyelectrolyte brushes

The simple scaling theory of weakly-charged polyelectrolyte brush (the layer of polyelectrolyte chains grafted at one end onto an impermeable surface) immersed into a good solvent has been developed.The asymptotic scaling dependences of the free layer thickness on charge density and solvent strength are obtained. The behavior of polyelectrolyte brush subjected to normal and tangential external forces is considered. New “polyelectrolyte effect” is predicted: shear of a free polyelectrolyte brush leads to a decrease in brush thickness in contrast to the case of a free neutral brush. Such behavior is equivalent to that of a neutral brush subjected to external normal stretching force. This force in the case of polyelectrolyte brush is created by the osmotic pressure of mobile counterions neutralizing grafted chain charges.     

Investigation of the mechanism of reaction of S-ethyl-N,N′-tetraethyldiamidothio-phosphite with [C5H 5Mn(CO)2NO]+BF by fourier transform infrared spectroscopy

FT-IR spectroscopy and a special mathematical program were used for the real-time monitoring of the mechanistic path of the reaction of S-ethyl-N,N-tetraethyldiamidothiophosphite with [CpMn(CO)-₂NO]⁺BFequation/tex2gif-stack-3.gif. The formation of a few intermediates is described.