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Substituent effects on the binding constants of arsenical-dithiol adducts
K Dill1, L H Huang, E L McGown
1Department of Chemistry, Clemson University, SC 29634-1905.
Abstract:
Proton nuclear magnetic resonance spectroscopy (1H NMR) was used to determine the relative binding constants for several arsenical-dithiol adducts. The compounds investigated were 2,3-dimercaptopropanol (British anti-lewisite; BAL), 1,2-ethane dithiol (ET), and 1,2-propane dithiol (PDT). It was found that PDT has a significantly higher affinity than ET or BAL for phenyldichloroarsine (PDA) in methanol.
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