Semi-empirical topological index: Development of QSPR/QSRR and optimization for alkylbenzenes
| Autor: | Vilma Edite Fonseca Heinzen, Berenice da Silva Junkes, Rosendo A. Yunes, Érica Silva Souza, Ledilege Cucco Porto |
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| Rok vydání: | 2008 |
| Předmět: |
Octanol
Chromatography Quantitative structure–activity relationship Correlation coefficient Analytical chemistry Quantitative Structure-Activity Relationship Analytical Chemistry Partition coefficient chemistry.chemical_compound chemistry Molar refractivity Squalane Topological index Benzene Derivatives Methods Alkylbenzenes |
| Zdroj: | Talanta. 76:407-412 |
| ISSN: | 0039-9140 |
| DOI: | 10.1016/j.talanta.2008.03.023 |
| Popis: | The semi-empirical topological index, IET, was developed and optimized to describe the chromatographic retention of alkylbenzenes on the squalane stationary phase. The simple linear regression between the chromatographic retention and the proposed index, for 122 alkylbenzenes studied, is of good quality (determination coefficient, r2 = 0.9996, standard deviation, S.D. = 5.5, and leave-one-out cross-validation correlation coefficient, r CV 2 = 0.9996 ). The predictive ability of IET was also verified for stationary phases with two different polarities (SE-30 and Carbowax 20 M), and good results were obtained, especially for the stationary phase with low polarity, showing that the specific molecular interactions occur on highly polar phases. The IET was applied to construct quantitative structure–property relationship (QSPR) models for representative properties such as boiling point, Bp(°C), octanol/water partition coefficient, log P, van der Waals volume (VW) and molar refractivity (RM). Satisfactory quality QSPR models were obtained with Bp, VW and RM showing that the molecular size and dispersive forces are dominating factors with respect to the chromatographic retention. |
| Databáze: | OpenAIRE |
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