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RESEARCH PRODUCT

Molecular topology and chromatographic retention parameters for benzodiazepines

F.pérez GiménezJ. Galvez AlvarezR. Garcia DomenechG.m. Antón FosF. Garcia MarchR. M. Soler Roca

subject

ChromatographyMolecular modelChemistrySilica gelOrganic ChemistryZero (complex analysis)Analytical chemistryGeneral MedicineFunction (mathematics)BiochemistryThin-layer chromatographyAnalytical Chemistrychemistry.chemical_compoundPolarMultiple correlationGas chromatography

description

Abstract The relationship between gas-liquid chromatographic (GLC) retention properties and R F values in thin-layer chromatography (TLC) with molecular connectivity indices, m X t , was investigated for a series of benzodiazepines using multiple correlation coefficients, standard errors of estimate, F -Snedecor function values and Student's t -test as the criteria for best equation selection. Regression analyses show that the molecular connectivity model predicts the retention properties in GLC with the polar stationary phase OV-17 at 280°C and the R F values in TLC with the stationary phase silica gel. However, zero- or second-order connectivity indices alone are not sufficient; higher-order indices are shown to be necessary. The effect of the polarity of the mobile phases in TLC was also investigated.

https://doi.org/10.1016/0021-9673(92)87057-f