Chromophores with quinoxaline core in π-bridge and aniline or carbazole donor moiety: synthesis and comparison of their linear and nonlinear optical properties

Russian Chemical Bulletin - Two new D—π—A chromophores with the tricyanofuranyl acceptor (A), an amphi-divinyl quinoxaline π-electron conjugated bridge, and the carbazole or...     

Regioselective heterocyclization of mixed phosphonium-iodonium ylides with acetylenes involving dimethyl acetylenedicarboxylate

Russian Chemical Bulletin - A new approach to the synthesis of λ5-phosphinolines was developed consisting in the reaction of mixed phosphonium-iodonium ylides with acetylenes in the presence...     

Preparation and characterization of microcapsules loaded with polyphenols-enriched Uncaria tomentosa extract using spray-dryer technique

Journal of Thermal Analysis and Calorimetry - This work prepared and characterized microcapsule of Uncaria tomentosa (UT) in order to standardize a spray-dryer Uncaria tomentosa extract. The UT...     

Shear modulus of single wood pulp fibers from torsion tests

Cellulose - The shear modulus of pulp fibers is difficult to measure and only very little literature is available on this topic. In this work we are introducing a method to measure this fiber...     

The Chemical Bond: When Atom Size Instead of Electronegativity Difference Determines Trend in Bond Strength

We have quantum chemically analyzed element−element bonds of archetypal H_nX−YH_n molecules (X, Y=C, N, O, F, Si, P, S, Cl, Br, I), using density functional theory. One purpose is to obtain a set of consistent homolytic bond dissociation energies (BDE) for establishing accurate trends across the periodic table. The main objective is to elucidate the underlying physical factors behind these chemical bonding trends. On one hand, we confirm that, along a period (e. g., from C−C to C−F), bonds strengthen because the electronegativity difference across the bond increases. But, down a period, our findings constitute a paradigm shift. From C−F to C−I, for example, bonds do become weaker, however, not because of the decreasing electronegativity difference. Instead, we show that the effective atom size (via steric Pauli repulsion) is the causal factor behind bond weakening in this series, and behind the weakening in orbital interactions at the equilibrium distance. We discuss the actual bonding mechanism and the importance of analyzing this mechanism as a function of the bond distance.     

Synthesis and Conductivity of Bismuth Molybdates Doped with Antimony and Tin

Russian Journal of Electrochemistry - The possibility of synthesizing oxygen-ion conductors based on bismuth molybdate with antimony and tin substituted to the molybdenum sublattice is studied and...     

Synthesis,structure, and properties of 2-[(4,6-di-tert-butyl-2,3-dihydroxyphenyl)thio]acetic acid amides

Russian Chemical Bulletin - New potential biologically active derivatives, in which the sterically hindered pyrocatechol moiety is linked through a 2-thioacetyl covalent bridge to a number of...     

Synthesis and biological properties of novel structural analogs of isothiobarbamine

Russian Chemical Bulletin - Novel structural analogs of isothiobarbamine, which differ from the prototype scaffold by the substituent at position 2 of the pyrimidine heterocycle, were for the first...     

Kinetic regularities of thermal decomposition of polycarbonate films containing Pt,Au, Ag,and Ni nanoparticles

Russian Chemical Bulletin - The kinetic regularities of thermal destruction of polycarbonate films containing Pt, Au, Ag, and Ni nanoparticles were studied. Scanning and transmission electron...     

Specific features of coupling reactions of polystyrene in the presence α-dinitrones based on glyoxal

Russian Chemical Bulletin - Bromine-containing polystyrene synthesized by atom transfer radical polymerization was used as a model to study coupling reactions in the presence of such free radical...