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Ewa Kaczmarczyk

Researcher at University of Gdańsk

Publications -  10
Citations -  82

Ewa Kaczmarczyk is an academic researcher from University of Gdańsk. The author has contributed to research in topics: Cationic polymerization & Pyridine. The author has an hindex of 7, co-authored 10 publications receiving 82 citations.

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A study of cationic heteroconjugation equilibria of substituted pyridine N-oxides in acetonitrile

TL;DR: In this paper, the formation of the [OH…O]+ hydrogen-bonded bridges of proton-Noxide systems in acetonitrile (a polar aprotic protophobic solvent) was studied using the potentiometric titration method.
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A potentiometric study of cationic heteroconjugation equilibria in systems with substituted pyridine N-oxides in nitrobenzene

TL;DR: In this article, a comparison of the cationic heteroconjugation constants in nitrobenzene with those measured in other non-aqueous solvents was made.
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A potentiometric study of cationic heteroconjugation equilibria in nitromethane andN,N- dimethylformamide

TL;DR: In this article, Cationic standard homoconjugation constants were determined in systems containing heterocyclic and aliphatic amine N -oxides, and pyridine, in two polar aprotic solvents: weakly basic protophobic nitromethane (NM); and strongly basic protophilic N, N -dimethylformamide (DMF).
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Potentiometric determination of standard acidity and cationic standard homoconjugation constants of substituted pyridine N-oxide systems in (acetonitrile + methanol)

TL;DR: In this article, an attempt has been made to determine potentiometrically standard acidityKao (BH + ) constants of protonated substituted pyridine N-oxides and cationic standard homoconjugation constantsKfo (BHB + ) of these acids conjugated with the Noxides in a binary solvent system.
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Studies on acid–base equilibria of 4-R-2,6-dimethylpyridine N-oxide systems in non-aqueous solvents

TL;DR: In this article, the acidity constant values of protonated N-oxides in polar nonaqueous solvents were determined, and it was found that the cationic homo-and heteroconjugation constant values increased with decreasing solvent basicity and with increasing basicity of the N-oxide.