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Article type: Research Article
Authors: Ioannou, Panayiotis V. | Vachliotis, Dimitris G. | Kouli, Ourania
Affiliations: Department of Chemistry, University of Patras, Patras, Greece | Department of Chemical Engineering, University of Patras, Patras, Greece
Note: [] Corresponding author: Panayiotis V. Ioannou, Department of Chemistry, University of Patras, Patras, Greece. Fax: +30 2610 997118; E-mail: [email protected]
Abstract: The α,β-dithiol 2,3-dimercapto-1-propanol (dimercaprol or British Anti-Lewisite, BAL) reacts with AsCl3, in a 1:1 molar ratio, giving the expected cyclic adduct 1 but with As2O3 and with AsCl3, in 2:3 As/BAL molar ratios, gave gums composed of many compounds. BAL reacts with Sb2O3 in DMSO but the products could not be isolated. With SbCl3 two products 2 and 3 have been isolated in 1:1 and 2:3 Sb/BAL molar ratios. Bi2O3 in 1:1 and 2:3 molar ratios gave compounds 4 and 5. However, BiCl3 and Bi(NO3)3·5H2O in either 1:1 or 2:3 stoichiometries gave compounds 6 and 7, respectively, indicating that the >Bi-Cl and >Bi(NO3) bonds were not reactive towards excess BAL. The 1H and 13C NMR spectra of the Sb(III) and Bi(III) complexes in DMSO-d6 revealed broad signals attributed to the quadrupole relaxation of Sb and Bi nuclei. No relaxation was observed for the arsenic complex 1 in CD3OD. Other properties of the complexes are presented and discussed.
Keywords: 2,3-Dimercapto-1-propanol, dimercaprol, British Anti-Lewisite, complexes with As(III), Sb(III) and Bi(III), $^1$H NMR, $^{13}$C NMR
DOI: 10.3233/MGC-130103
Journal: Main Group Chemistry, vol. 12, no. 3, pp. 235-249, 2013
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