<p> In the first part, the preparation and properties of chalcogen-containing vitamin E analogues are described. The sulfur compound 3,3,4,6,7-pentamethyl-2,3-dihydrobenzo[<i>b</i>]thiophene-5-ol was prepared by two different routes using ionic and radical chemistry. Interesting rearrangements were observed in the two synthetic pathways. </p><p> A new methodology for the synthesis of dihydroselenophene and dihydrotellurophene derivatives is described. In the preparation of the vitamin E analogues 2,3-dihydrobenzo[<i>b</i>]selenophene-5-ol and 2,3-dihydrobenzo[<i>b</i>]tellurophene-5-ol a tellurium-mediated tandem S<sub>RN</sub>1/S<sub>H</sub>i sequence was suggested to be operative. 2,3-Dihydrobenzo[<i>b</i>]thiophene-5-ol and the vitamin E-like selenide 2-methyl-2-(4,8,12-trimethyl-tridecyl)-selenochroman-6-ol were prepared via intramolecular homolytic substitution at sulfur and selenium, respectively. The first rate constant for intramolecular homolytic substitution at tellurium is also reported (5x10<sup>8 </sup>s<sup>-1</sup> at 25 °C).</p><p> The antioxidant profile for 2,3-dihydrobenzo[<i>b</i>]furan-5-ol and its 1-thio, 1-seleno, and 1-telluro analogues is described. By means of pulse radiolysis, it was shown that the one-electron reduction potentials (ArO·/ArO<sup>-</sup>) were independent of the chalcogen (0.49-0.52 V vs NHE). The O-H bond dissociation enthalpies for the compounds were also estimated to be similar (336-340 kJ mol<sup>-1</sup>). The p<i>K</i><sub>a</sub> values and the oxidation potentials were also determined for these compounds. For some compounds the rate of hydrogen atom donation to <i>tert</i>-butoxyl radicals was determined by means of laser flash photolysis. Using a two-phase lipid peroxidation model, it was demonstrated that the selenium and tellurium analogues could be regenerated in the presence of a stoichiometric amount of a reducing agent. The organotellurium analogue also acted as a good glutathione-peroxidase mimic and as a potent inhibitor of lipid peroxidation in liver microsomes. </p><p> In the second part of the thesis the stabilizing capacity of bis[4-(dimethylamino)phenyl]telluride was investigated in the thermoplastic elastomer PACREL<sup>®</sup>. It was demonstrated that the addition of 0.17-0.50 % of the telluride significantly improved the tensile strength and elongation at break of the polymer. Chemiluminescence measurements showed that the organotellurium compound prolonged the induction period of thermo-oxidation and reduced the total luminescence intensity of the material.</p>
| Identifer | oai:union.ndltd.org:UPSALLA/oai:DiVA.org:uu-1085 |
| Date | January 2000 |
| Creators | Malmström, Jonas |
| Publisher | Uppsala University, Department of Chemistry, Uppsala : Acta Universitatis Upsaliensis |
| Source Sets | DiVA Archive at Upsalla University |
| Language | English |
| Detected Language | English |
| Type | Doctoral thesis, comprehensive summary, text |
| Relation | Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, 1104-232X ; 588 |
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