Standard

Features of the recurrent approximation of retention parameters of polyfunctional compounds in reversed-phase high performance liquid chromatography. / Зенкевич, Игорь Георгиевич; Никитина, Дарья Александровна.

в: Russian Journal of Physical Chemistry A, Том 95, № 2, 01.02.2021, стр. 395-402.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

APA

Vancouver

Author

BibTeX

@article{4cda3491c6814b4cb5c9ad42892f6261,
title = "Features of the recurrent approximation of retention parameters of polyfunctional compounds in reversed-phase high performance liquid chromatography",
abstract = "Abstract: Five antitumor drugs are selected as examples of polyfunctional organic compounds to test the possibilities of approximating their retention parameters in reversed-phase high-performance liquid chromatography using recurrent relationships of the form of t R(C + ΔС) = at R(C) + b, where C is the concentration of organic modifier in the composition of the eluent (acetonitrile), ΔC = const is a constant step of its change in concentration, and a and b are coefficients calculated using the least squares method. Examples of both ideally linear dependences in all ranges of acetonitrile concentrations and deviations from linearity in different ranges of its concentrations are revealed. Discussion of the possible reasons for such deviations (both structural factors and physicochemical properties) suggests that acid–base equilibria in the eluent are not the main ones, the positions of which depend on the concentration of the organic component. The reversible formation of hydrated forms typical of compounds whose molecules contain such polar fragments as amide ‒CO–NH– and sulfonamide –SO 2–NH groups, seems more likely. Recurrent approximation of the retention parameters can be considered the simplest and most obvious way to reveal the specific interactions of the test compounds with components of the eluent. ",
keywords = "Приведены в тексте статьи, HPLC, Formation of hydrates, reversed-phase high-performance liquid chromatography, polyfunctional organic compounds, deviations from linearity, formation of hydrated forms, recurrent approximation of retention parameters",
author = "Зенкевич, {Игорь Георгиевич} and Никитина, {Дарья Александровна}",
note = "Zenkevich I.G., Nikitina D.A. J. Phys. Chem. A. (Rus.). 2021. V. 95. № 2. P. 395-402.",
year = "2021",
month = feb,
day = "1",
doi = "10.1134/s003602442102028x",
language = "English",
volume = "95",
pages = "395--402",
journal = "Russian Journal of Physical Chemistry A",
issn = "0036-0244",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "2",

}

RIS

TY - JOUR

T1 - Features of the recurrent approximation of retention parameters of polyfunctional compounds in reversed-phase high performance liquid chromatography

AU - Зенкевич, Игорь Георгиевич

AU - Никитина, Дарья Александровна

N1 - Zenkevich I.G., Nikitina D.A. J. Phys. Chem. A. (Rus.). 2021. V. 95. № 2. P. 395-402.

PY - 2021/2/1

Y1 - 2021/2/1

N2 - Abstract: Five antitumor drugs are selected as examples of polyfunctional organic compounds to test the possibilities of approximating their retention parameters in reversed-phase high-performance liquid chromatography using recurrent relationships of the form of t R(C + ΔС) = at R(C) + b, where C is the concentration of organic modifier in the composition of the eluent (acetonitrile), ΔC = const is a constant step of its change in concentration, and a and b are coefficients calculated using the least squares method. Examples of both ideally linear dependences in all ranges of acetonitrile concentrations and deviations from linearity in different ranges of its concentrations are revealed. Discussion of the possible reasons for such deviations (both structural factors and physicochemical properties) suggests that acid–base equilibria in the eluent are not the main ones, the positions of which depend on the concentration of the organic component. The reversible formation of hydrated forms typical of compounds whose molecules contain such polar fragments as amide ‒CO–NH– and sulfonamide –SO 2–NH groups, seems more likely. Recurrent approximation of the retention parameters can be considered the simplest and most obvious way to reveal the specific interactions of the test compounds with components of the eluent.

AB - Abstract: Five antitumor drugs are selected as examples of polyfunctional organic compounds to test the possibilities of approximating their retention parameters in reversed-phase high-performance liquid chromatography using recurrent relationships of the form of t R(C + ΔС) = at R(C) + b, where C is the concentration of organic modifier in the composition of the eluent (acetonitrile), ΔC = const is a constant step of its change in concentration, and a and b are coefficients calculated using the least squares method. Examples of both ideally linear dependences in all ranges of acetonitrile concentrations and deviations from linearity in different ranges of its concentrations are revealed. Discussion of the possible reasons for such deviations (both structural factors and physicochemical properties) suggests that acid–base equilibria in the eluent are not the main ones, the positions of which depend on the concentration of the organic component. The reversible formation of hydrated forms typical of compounds whose molecules contain such polar fragments as amide ‒CO–NH– and sulfonamide –SO 2–NH groups, seems more likely. Recurrent approximation of the retention parameters can be considered the simplest and most obvious way to reveal the specific interactions of the test compounds with components of the eluent.

KW - Приведены в тексте статьи

KW - HPLC

KW - Formation of hydrates

KW - reversed-phase high-performance liquid chromatography

KW - polyfunctional organic compounds

KW - deviations from linearity

KW - formation of hydrated forms

KW - recurrent approximation of retention parameters

UR - http://www.scopus.com/inward/record.url?scp=85102387238&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/97a46b62-0c9f-3d1a-878b-b398ce72f301/

U2 - 10.1134/s003602442102028x

DO - 10.1134/s003602442102028x

M3 - Article

VL - 95

SP - 395

EP - 402

JO - Russian Journal of Physical Chemistry A

JF - Russian Journal of Physical Chemistry A

SN - 0036-0244

IS - 2

ER -

ID: 74451540