Copolymerization of N-vinylpyrrole-2-carbaldehydes with styrene, N-vinylpyrrolidone, and ethylene glycol vinyl glycidyl ether

Polyfunctional reactive copolymers of N-vinylpyrrole-2-carbaldehydes with styrene, N-vinylpyrrolidone, and ethylene glycol vinyl glycidyl ether are synthesized in the presence of AIBN (2 wt %, 80°C, 50 h) with a yield of up to 98% and a molecular mass of up to 4800. The copolymers show paramagnetic behavior (N = 2.0 × 10¹⁵?2.0 × 10¹⁷ g^?1) and possess the properties of organic semiconductors (σ = 0.9 × 10^?11–2.8 × 10^?7 S/cm after doping with I₂).     

Polymerization of 1,4-bis[2-(N-vinyl)pyrrolyl]benzene

Polymers of 1,4-bis[2-(N-vinyl)pyrrolyl]benzene with free N-vinyl groups in side chains are synthesized in the presence of AIBN (2–5 wt %, 70°C) with a yield of up to 34% and a molecular mass of up to 11.5 × 10³. In the presence of cationic catalysts (Me₃SiCl, the LiBF₄-dimethoxyethane system, and BF₃ · OEt₂), 1,4-bis[2-(N-vinyl)pyrrolyl]benzene gives macromolecules with alternating 1,2-pyrrolene and ethylidene units in the backbone with yields of 80, 44, and 33%, respectively. The polymers demonstrate paramagnetic and luminescent properties.     

Synthesis of 3- and 5-amino-5-(3)-(pyrrol-2-yl)isoxazoles

5-Amino-3-(pyrrol-2-yl)isoxazoles were selectively prepared by the reaction of 2-(2,2-dicyano-1-ethylthioethenyl)pyrroles with hydroxylamine in methanol. Under analogous conditions, 2-(2-carbamoyl-2-cyano-1-ethylthioethenyl) pyrroles with hydroxylamine gave 5-aminoisoxazoles and their structural isomers, 3-aminoisoxazoles (3-5% yield). The latter were selectively prepared by reacting 2-(2-carbamoyl-2-cyano-1-ethylthioethenyl)pyrroles with hydroxylamine in the presence of aqueous NaOH and from the products of intramolecular cyclization of 2-(2-carbamoyl-2-cyano-1-ethylthioethenyl)pyrroles, 1-ethylthio-3-iminopyrrolizines and hydroxylamine.     

Base‐Catalyzed Stereoselective Vinylation of Ketones with Arylacetylenes: A New C(sp3)?C(sp2) Bond‐Forming Reaction

Alkylaryl‐ and alkylheteroarylketones, including those with condensed aromatic moieties, are readily vinylated with arylacetylenes (KOH/DMSO, 100 °C, 1 h) to give regio‐ and stereoselectively the (E)‐β‐γ‐ethylenic ketones ((E)‐3‐buten‐1‐ones) in 61–84 % yields and with approximately 100 % stereoselectivity. This vinylation represents a new C(sp³)? C(sp²) bond‐forming reaction of high synthetic potential.     

Algebraic multilevel method AMG: Comparison with the method BICGSTAB + ILU and its use in the method CPR

The algebraic multilevel method AMG is compared with the method BICGSTAB+ILU on a model problem with a strong anisotropy. The method AMG was used as a part of the method CPR for solution of the filtration problems of a viscous compressible fluid flow in porous media. The algorithm CPR+AMG is compared with CPR+ILU on the base of this problem. The work of the CPR+AMG is analyzed by solving the problem for a model oil field.     

Chemical physics of cellulose nitration

The physical mechanisms responsible for the kinetics of nitration of cellulose raw materials of different origin have been studied. It has been shown that the main nitration rate-limiting factor is the speed of untwisting of supercoiled cellulose fibers. This process limits the penetration of nitrating agents into microcrystalline regions and, thus, the total reaction rate. The constructed physical model provides an adequate explanation of all the experimentally observed features of the cellulose nitration process, particularly as a function of cellulose origin (cotton, flax, wood) and preparation/treatment methods (sulfite, sulfate, bleached, refined with sulfurous or boric acids or acetone). The theoretical results have been tested in practice.