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The Influence of the Aromaticity in the Gas Chromatography Retention: The Case of Polycyclic Aromatic Sulfur Heterocycles
Published
Author(s)
Jorge O. Ona-Ruales, Yosadara Ruiz-Morales, Fernando Alvarez-Ramirez, Walter Brent Wilson, Stephen A. Wise
Abstract
The aromaticity has been used as a criterion to explain the GC retention of cata-condensed polycyclic aromatic sulfur heterocycles (PASHs) C12H8S, C16H10S, C20H12S; and peri-condensed PASHs C18H10S, in a GC column with 50% phenyl / 50% methyl silphenylene polymer. To establish the aromaticity, Nucleus-Independent Chemical Shifts at the level of the molecular plane, NICS(0), and at 1 Å above the surface of the molecular plane, NICS(1), have been used. It has been found that the GC retention of cata-condensed PASHs C12H8S, C16H10S, and C20H12S is satisfactorily defined by the aromaticity of the entire molecule, and the GC retention of peri-condensed PASHs C18H10S is satisfactorily defined by the local aromaticity in the sulfur pentagonal ring. In addition, the positive slope between GC retention and NICS(0) of the entire molecule for cata-condensed PASHs, C12H8S and C16H10S, and by NICS(1) in the pentagonal ring for peri-condensed PASHs, C18H10S, is explained by the interaction between the electrons of the heterocycle molecule and the positive pole of the silicon atom in the GC column, as it was suggested with PAHs. In opposition to this, the negative slope between GC retention and aromaticity for cata-condensed C20H12S is explained because of the absence or presence of bay, cove, or fjord regions in the vicinity of the sulfur atom that generates lower aromaticity resulting in increased GC retention or higher aromaticity resulting in decreased GC retention.
Ona-Ruales, J.
, Ruiz-Morales, Y.
, Alvarez-Ramirez, F.
, Wilson, W.
and Wise, S.
(2017),
The Influence of the Aromaticity in the Gas Chromatography Retention: The Case of Polycyclic Aromatic Sulfur Heterocycles, Chromatographia, [online], https://doi.org/10.1007/s10337-017-3465-1
(Accessed October 10, 2024)