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Retention behavior of alkyl-substituted polycyclic aromatic sulfur heterocycles in reversed-phase liquid chromatography

机译:烷基取代的多环芳族硫杂环在反相液相色谱中的保留行为

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摘要

Retention indices for 79 alkyl-substituted polycyclic aromatic sulfur heterocycles (PASHs) were determined by using reversed-phase liquid chromatography (LC) on a monomeric and polymeric octadecylsilane (C18) stationary phase. Molecular shape parameters [length, breadth, thickness (T), and length-to-breadth ratio (L/B)] were calculated for all the compounds studied. Based on separations of isomeric methylated polycyclic aromatic hydrocarbons on polymeric C18 phases, alkyl-substituted PASHs are expected to elute based on increasing L/B ratios. However, the correlation coefficients had a wide range of values from r = 0.43 to r = 0.93. Several structural features besides L/B ratios were identified to play an important role in the separation mechanism of PASHs on polymeric C18 phases. First, the location of the sulfur atom in a bay-like-region results in alkylated-PASHs being more retentive than non-bay-like-region alkylated-PASHs, and they elute later than expected based on L/B value. Second, the placement of the alkyl group in the k region of the structure resulted in a later elution than predicted by L/B. Third, highly nonplanar methyl-PASHs (i.e., 1-Me and 11-MeBbN12T) elute prior to the parent PASH (BbN12T).
机译:通过在单体和聚合十八烷基硅烷(C18)固定相上使用反相液相色谱(LC),确定79个烷基取代的多环芳族硫杂环(PASH)的保留指数。计算了所有研究化合物的分子形状参数[长度,宽度,厚度(T)和长宽比(L / B)]。基于在聚合的C18相上分离出的异构甲基化多环芳烃,随着L / B比的增加,烷基取代的PASH有望被洗脱。但是,相关系数的取值范围从r = 0.43到r = 0.93。可以确定L / B比率以外的几种结构特征在聚合物C18相上PASH的分离机理中也起着重要作用。首先,硫原子在海湾状区域中的位置导致烷基化的PASH比非海湾状区域的烷基化PASH更具保留性,并且洗脱时间比基于L / B值的预期要晚。其次,烷基在结构的k区的放置导致洗脱时间比L / B预测的时间晚。第三,高度非平面的甲基-PASH(即1-Me和11-MeBbN12T)在母体PASH(BbN12T)之前洗脱。

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