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|Title:||Spectrophotometric Studies of the Complexation of 2-Aryl-Imino-N-(2-Aryl)-Thiazoline Substrates with Hydroxypropyl Cyclodextrin||Authors:||Hassan, Inas EL
Zeine, Abdel Razzak El
Abou Dalle, Adib
Nakat, Hanna El
Omar, Fawaz El
|Affiliations:||Department of Chemistry||Keywords:||2-aryl-imino-N-(2-aryl)-thiazoline
|Issue Date:||2012||Part of:||International journal of chemical sciences||Volume:||10||Issue:||1||Start page:||463||End page:||471||Abstract:||
Cyclodextrins molecules can form inclusion complexes with a wide variety of substrates. The relatively hydrophobic cavity of native cyclodextrins and their derivatives induces the ability to complex substrates of appropriate size and shape. Complexation of substrates with cyclodextrins can modify the solubility of the substrate and increase its stability. The most common application of CD in pharmaceutical industry is to enhance drug solubility in aqueous solutions. Inclusion complexes of 2 (2-aryl-imino-N-(2- aryl)-thiazoline) substrates: N-[(2Z)-4-methyl-3-(2-methylphenyl)-1,3-thiazol-2(3H)-ylidene]-N-(2-chlorophenyl) amine (1) and N-[(2Z)-4-methyl-3-(2-methylphenyl)-1,3-thiazol-2(3H)-ylidene]-N-(2-chloro-4 nitrophenyl) amine (2) with hydroxypropyl-γ-cyclodextrin (HPγCD) were investigated by applying a simple and rapid spectrophotometric methods. The 1 : 1 stoichiometry of substrate-CD complexes were determined by continuous variation (Job's plot) method and the overall association constants were determined by using Scott's method. The association constants were determined to be 30866 M-1 and 5765 M-1 respectively.
|URI:||https://scholarhub.balamand.edu.lb/handle/uob/2561||Open URL:||Link to full text||Type:||Journal Article|
|Appears in Collections:||Department of Chemistry|
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