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Article type: Research Article
Authors: Ioannou, P.V.
Affiliations: Department of Chemistry, University of Patras, Patras, Greece
Note: [] Corresponding author: Fax: +30 610 997118; E-mail: [email protected]
Abstract: The reaction of para-substituted thiophenols with Bi(NO3)3ċ5H2O and BiO(NO3)ċH2O was studied. The nitrate was more reactive than the subnitrate, and was a convenient bismuth compound for the preparation of trithiolates, Bi(SAr)3. Thiols having electron withdrawing groups seem to be more reactive than those with electron donating groups. The thiolato groups in Bi(SAr)3 can migrate to Bi(NO3)3ċ5H2O thus giving (ArS)2Bi(NO3), but the monothiolate product, ArS-Bi(NO3)2, decomposed evolving NO2. Bi(III) complexes with some aromatic thiols of probable biochemical interest are also described.
Keywords: Bismuth nitrate pentahydrate, bismuth subnitrate monohydrate, para-substituted thiophenols, 2-pyridinethiol, 2-pyridinethiol N-oxide
DOI: 10.3233/MGC-2011-0053
Journal: Main Group Chemistry, vol. 10, no. 3-4, pp. 255-264, 2011
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