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Study of methyl- and phenyl-substituted thermostable polysiloxane–silarylene motionless phases for capillary gas chromatography. / Komarova, A. O.; Shashkov, M. V.; Sidel’nikov, V. N.

In: Russian Journal of Physical Chemistry A, Vol. 91, No. 11, 01.11.2017, p. 2252-2259.

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Komarova AO, Shashkov MV, Sidel’nikov VN. Study of methyl- and phenyl-substituted thermostable polysiloxane–silarylene motionless phases for capillary gas chromatography. Russian Journal of Physical Chemistry A. 2017 Nov 1;91(11):2252-2259. doi: 10.1134/S0036024417110103

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@article{98dbc93d97df47498814362b2d11e7f4,
title = "Study of methyl- and phenyl-substituted thermostable polysiloxane–silarylene motionless phases for capillary gas chromatography",
abstract = "Capillary columns based on a number of thermostable polysiloxane–silarylene motionless phases are prepared and their properties are studied. Three polymers with different contents of methyl and phenyl groups are synthesized: dimethylsiloxanesilarylene (DMS), methylphenylsiloxanesilarylene (MPhS), and diphenylsiloxanesilarylene (DPhS). Studies of their thermostability show that the level of the background current of these columns upon heating to 350°С is several times lower than that of a column based on polydimethylsiloxane. Based on McReynolds{\textquoteright} studies of polarity and Abraham{\textquoteright}s studies of the selectivity of prepared columns according to the parameters of intermolecular interactions, it is found that silarylene MLPs are more affected by the contributions from specific interactions (especially for dipole-dipole, -, and n–π-interactions) than MLPs with no phenylеne inserts. The effect on the selectivity of a phenyl group inside a chain differs from the one produced by the phenyl groups in side MLP chains. The effect on the selectivity of a phenyl group inside a chain differs from the one produced by the phenyl groups in side MLP chains. Examples of the separation of test mixtures of aromatic and oxygen-containing compounds are obtained, along with an extract of thistle oil containing tocopherols and phytosterols at a final temperature of analysis of 350°С.",
keywords = "gas chromatography, motionless liquid phases, polysiloxane polymers, thermostability, POLYMERS, POLYMETHYLHYDROSILOXANES, STATIONARY PHASES, COPOLYMERS, THERMAL-DEGRADATION, POLY(TETRAMETHYL-PARA-SILPHENYLENE SILOXANE), COLUMNS, DIMETHYLSILOXANE, SEPARATION CHARACTERISTICS, DEACTIVATION",
author = "Komarova, {A. O.} and Shashkov, {M. V.} and Sidel{\textquoteright}nikov, {V. N.}",
year = "2017",
month = nov,
day = "1",
doi = "10.1134/S0036024417110103",
language = "English",
volume = "91",
pages = "2252--2259",
journal = "Russian Journal of Physical Chemistry A",
issn = "0036-0244",
publisher = "PLEIADES PUBLISHING INC",
number = "11",

}

RIS

TY - JOUR

T1 - Study of methyl- and phenyl-substituted thermostable polysiloxane–silarylene motionless phases for capillary gas chromatography

AU - Komarova, A. O.

AU - Shashkov, M. V.

AU - Sidel’nikov, V. N.

PY - 2017/11/1

Y1 - 2017/11/1

N2 - Capillary columns based on a number of thermostable polysiloxane–silarylene motionless phases are prepared and their properties are studied. Three polymers with different contents of methyl and phenyl groups are synthesized: dimethylsiloxanesilarylene (DMS), methylphenylsiloxanesilarylene (MPhS), and diphenylsiloxanesilarylene (DPhS). Studies of their thermostability show that the level of the background current of these columns upon heating to 350°С is several times lower than that of a column based on polydimethylsiloxane. Based on McReynolds’ studies of polarity and Abraham’s studies of the selectivity of prepared columns according to the parameters of intermolecular interactions, it is found that silarylene MLPs are more affected by the contributions from specific interactions (especially for dipole-dipole, -, and n–π-interactions) than MLPs with no phenylеne inserts. The effect on the selectivity of a phenyl group inside a chain differs from the one produced by the phenyl groups in side MLP chains. The effect on the selectivity of a phenyl group inside a chain differs from the one produced by the phenyl groups in side MLP chains. Examples of the separation of test mixtures of aromatic and oxygen-containing compounds are obtained, along with an extract of thistle oil containing tocopherols and phytosterols at a final temperature of analysis of 350°С.

AB - Capillary columns based on a number of thermostable polysiloxane–silarylene motionless phases are prepared and their properties are studied. Three polymers with different contents of methyl and phenyl groups are synthesized: dimethylsiloxanesilarylene (DMS), methylphenylsiloxanesilarylene (MPhS), and diphenylsiloxanesilarylene (DPhS). Studies of their thermostability show that the level of the background current of these columns upon heating to 350°С is several times lower than that of a column based on polydimethylsiloxane. Based on McReynolds’ studies of polarity and Abraham’s studies of the selectivity of prepared columns according to the parameters of intermolecular interactions, it is found that silarylene MLPs are more affected by the contributions from specific interactions (especially for dipole-dipole, -, and n–π-interactions) than MLPs with no phenylеne inserts. The effect on the selectivity of a phenyl group inside a chain differs from the one produced by the phenyl groups in side MLP chains. The effect on the selectivity of a phenyl group inside a chain differs from the one produced by the phenyl groups in side MLP chains. Examples of the separation of test mixtures of aromatic and oxygen-containing compounds are obtained, along with an extract of thistle oil containing tocopherols and phytosterols at a final temperature of analysis of 350°С.

KW - gas chromatography

KW - motionless liquid phases

KW - polysiloxane polymers

KW - thermostability

KW - POLYMERS

KW - POLYMETHYLHYDROSILOXANES

KW - STATIONARY PHASES

KW - COPOLYMERS

KW - THERMAL-DEGRADATION

KW - POLY(TETRAMETHYL-PARA-SILPHENYLENE SILOXANE)

KW - COLUMNS

KW - DIMETHYLSILOXANE

KW - SEPARATION CHARACTERISTICS

KW - DEACTIVATION

UR - http://www.scopus.com/inward/record.url?scp=85030149206&partnerID=8YFLogxK

U2 - 10.1134/S0036024417110103

DO - 10.1134/S0036024417110103

M3 - Article

AN - SCOPUS:85030149206

VL - 91

SP - 2252

EP - 2259

JO - Russian Journal of Physical Chemistry A

JF - Russian Journal of Physical Chemistry A

SN - 0036-0244

IS - 11

ER -

ID: 9033246