| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1232609 | Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy | 2012 | 4 Pages |
Interaction between thiazolidine-2-thione (T2T) as an electron donor and 2,3,5,6-tetrabromo-1,4-benzoquinone (p-bromanil, BRL) as a π-electron acceptor has been studied by using several spectral techniques, viz. UV/visible, IR, 1H NMR and Mass spectra. A substitution reaction has been occurred after an initial formation of a CT complex, meanwhile a redox reaction has been occurred, in situ, too in which the interacting donor (T2T) has been oxidized to the corresponding thiazole. Thus, the stoichiometric ratio of this interaction has been found to be 2:1, T2T:BRL. However, the most interesting finding is that unexpectedly neither the SH group of the thiol form nor the NH group of the thione form of the T2T has shared in the substitution reaction with BRL. This finding has been confirmed by the different applied spectral tools, whereas a plausible reaction pathway has been illustrated and discussed.
Graphical abstractThe interaction between thiazolidine-2-thione (T2T) as an electron donor and 2,3,5,6-tetrabromo-1,4-benzoquinone (p-bromanil, BRL) involves redox and substitution reactions after an initial formation of a CT complex. Unexpectedly, and interestingly too, neither the SH group of the thiol form nor the NH group of the thione form of the T2T has shared in the substitution reaction with BRL.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Thiazoline-2-thiol/BRL system gives sequential and multiple interactions. ► A CT complexation has been initially occurred. ► Both the thione and thiol forms have been oxidized to the corresponding thiazoles. ► The product of the substitution reaction has two tautomeric forms too.
