Linear Correlations of the Gas Chromatographic Retention Indices of Compounds from Various Taxonomic Groups
Despite the constant improvement of complex computer algorithms for the calculation of gas chromatographic retention indices (RIs), the simplest methods for their evaluation based on linear correlations between the indices of structural analogs from different taxonomic groups, RI 1 ≈ a RI 2 + b , re...
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Published in | Journal of analytical chemistry (New York, N.Y.) Vol. 78; no. 6; pp. 766 - 775 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Moscow
Pleiades Publishing
01.06.2023
Springer Springer Nature B.V |
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Abstract | Despite the constant improvement of complex computer algorithms for the calculation of gas chromatographic retention indices (RIs), the simplest methods for their evaluation based on linear correlations between the indices of structural analogs from different taxonomic groups, RI
1
≈
a
RI
2
+
b
, remain important. It is shown that symbatic variations of the first numerical differences of retention indices,
= RI
n
+ 1
– RI
n
(equivalent to the first derivatives of the retention indices with respect to the structural parameter varied in the group), are the conditions of correctness for such correlations in the simplest groups (substituted methanes). A monotonic variation of
in one of the groups with the presence of extrema in the other group is an unequivocal sign of the absence of a linear correlation between retention indices. If the values of
in one of the groups increase and decrease in the other, the ranking order of compounds in any one of them should be reversed. It is shown that the simplest relationship RI
1
≈
a
RI
2
+
b
is also applicable to more complex taxonomic groups (substituted ethanes, benzenes, and naphthalenes), and it allows one not only to estimate the RIs of compounds not yet characterized but also to refine known reference data. |
---|---|
AbstractList | Despite the constant improvement of complex computer algorithms for the calculation of gas chromatographic retention indices (RIs), the simplest methods for their evaluation based on linear correlations between the indices of structural analogs from different taxonomic groups, RI
1
≈
a
RI
2
+
b
, remain important. It is shown that symbatic variations of the first numerical differences of retention indices,
= RI
n
+ 1
– RI
n
(equivalent to the first derivatives of the retention indices with respect to the structural parameter varied in the group), are the conditions of correctness for such correlations in the simplest groups (substituted methanes). A monotonic variation of
in one of the groups with the presence of extrema in the other group is an unequivocal sign of the absence of a linear correlation between retention indices. If the values of
in one of the groups increase and decrease in the other, the ranking order of compounds in any one of them should be reversed. It is shown that the simplest relationship RI
1
≈
a
RI
2
+
b
is also applicable to more complex taxonomic groups (substituted ethanes, benzenes, and naphthalenes), and it allows one not only to estimate the RIs of compounds not yet characterized but also to refine known reference data. Despite the constant improvement of complex computer algorithms for the calculation of gas chromatographic retention indices (RIs), the simplest methods for their evaluation based on linear correlations between the indices of structural analogs from different taxonomic groups, RI1 ≈ aRI2 + b, remain important. It is shown that symbatic variations of the first numerical differences of retention indices, = RIn+ 1 – RIn (equivalent to the first derivatives of the retention indices with respect to the structural parameter varied in the group), are the conditions of correctness for such correlations in the simplest groups (substituted methanes). A monotonic variation of in one of the groups with the presence of extrema in the other group is an unequivocal sign of the absence of a linear correlation between retention indices. If the values of in one of the groups increase and decrease in the other, the ranking order of compounds in any one of them should be reversed. It is shown that the simplest relationship RI1 ≈ aRI2 + b is also applicable to more complex taxonomic groups (substituted ethanes, benzenes, and naphthalenes), and it allows one not only to estimate the RIs of compounds not yet characterized but also to refine known reference data. Despite the constant improvement of complex computer algorithms for the calculation of gas chromatographic retention indices (RIs), the simplest methods for their evaluation based on linear correlations between the indices of structural analogs from different taxonomic groups, RI.sup.1 [almost equal to] aRI.sup.2 + b, remain important. It is shown that symbatic variations of the first numerical differences of retention indices, [Formula omitted] = RI.sub.n.sub.+ 1 - RI.sub.n (equivalent to the first derivatives of the retention indices with respect to the structural parameter varied in the group), are the conditions of correctness for such correlations in the simplest groups (substituted methanes). A monotonic variation of [Formula omitted] in one of the groups with the presence of extrema in the other group is an unequivocal sign of the absence of a linear correlation between retention indices. If the values of [Formula omitted] in one of the groups increase and decrease in the other, the ranking order of compounds in any one of them should be reversed. It is shown that the simplest relationship RI.sup.1 [almost equal to] aRI.sup.2 + b is also applicable to more complex taxonomic groups (substituted ethanes, benzenes, and naphthalenes), and it allows one not only to estimate the RIs of compounds not yet characterized but also to refine known reference data. |
Audience | Academic |
Author | Zenkevich, I. G. |
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Cites_doi | 10.1007/BF02578124 10.1016/S0021-9673(01)87374-X 10.3390/ijms22179194 10.1109/ACCESS.2020.3045047 10.1016/j.chroma.2021.462100 10.1134/S1061934823010148 10.1016/chroma.2007.03.108 10.15866/iremos.v14i2.20460 10.1002/(SICI)1521-4168(19981001)21:10<565::AID-JHRC565>3.0.CO;2-6 10.1134/S0036024421040294 10.1016/j.chemolab.2004.01.012 10.1021/ci980036z 10.4172/2157-7064.1000306 10.1021/ci600548y 10.1134/S0022476613030050 10.1007/BF02437183 10.1134/S003602442107030X |
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Copyright | Pleiades Publishing, Ltd. 2023. ISSN 1061-9348, Journal of Analytical Chemistry, 2023, Vol. 78, No. 6, pp. 766–775. © Pleiades Publishing, Ltd., 2023. Russian Text © The Author(s), 2023, published in Zhurnal Analiticheskoi Khimii, 2023, Vol. 78, No. 6, pp. 528–537. COPYRIGHT 2023 Springer |
Copyright_xml | – notice: Pleiades Publishing, Ltd. 2023. ISSN 1061-9348, Journal of Analytical Chemistry, 2023, Vol. 78, No. 6, pp. 766–775. © Pleiades Publishing, Ltd., 2023. Russian Text © The Author(s), 2023, published in Zhurnal Analiticheskoi Khimii, 2023, Vol. 78, No. 6, pp. 528–537. – notice: COPYRIGHT 2023 Springer |
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Keywords | taxonomic groups of structural analogs linear correlation gas chromatographic retention indices index correctness control estimation of unknown values |
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SubjectTerms | Algorithms Analysis Analytical Chemistry Chemistry Chemistry and Materials Science Chromatography Correlation Correlation (Statistics) Gas chromatography Methods Retention Substitutes Taxonomy Zoological specimens |
Title | Linear Correlations of the Gas Chromatographic Retention Indices of Compounds from Various Taxonomic Groups |
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