文摘
Guest-host inclusion complexation formation between polycyclic aromatic hydrocarbons anthracene and anthracene chiral derivatives (1-(9-anthryl)-2,2,2-triflouroethanol (TFE)) and methyl-β-cyclodextrin (Me-β-CD) was examined using fluorescence spectroscopy Me-β-CD shows enantiomeric and chiral discrimination of TFE enantiomers. Emission spectra data of anthracene-Me-β-CD and enantiomers of TFE-Me-β-CD-guest-host inclusion complexes was used subjected to chemometric partial-least-square (PLS) regression analysis The values of calculated binding constants and negative ΔG suggest the thermodynamic favorability of anthracene-Me-β-CD and enantiomeric of TFE-Me-β-CD inclusion complexation reactions. The PLS regression analysis resulted in square-correlation-coefficients of ≥ 0.997530 and a low LOD of 3.48 × 10− 8M and accurately determined the anthracene and TFE enantiomer concentrations with low error of ≤ 4.5%.