THE RELATIVE REACTIVITY OF THIOETHERS AND SULFOXIDES TOWARD OXYGEN-TRANSFER REAGENTS - THE OXIDATION OF THIANTHRENE 5-OXIDE AND RELATED-COMPOUNDS BY MOO(5)HMPT

Citation
M. Bonchio et al., THE RELATIVE REACTIVITY OF THIOETHERS AND SULFOXIDES TOWARD OXYGEN-TRANSFER REAGENTS - THE OXIDATION OF THIANTHRENE 5-OXIDE AND RELATED-COMPOUNDS BY MOO(5)HMPT, Journal of organic chemistry, 60(14), 1995, pp. 4475-4480
Citations number
35
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00223263
Volume
60
Issue
14
Year of publication
1995
Pages
4475 - 4480
Database
ISI
SICI code
0022-3263(1995)60:14<4475:TRROTA>2.0.ZU;2-0
Abstract
The oxidation of thianthrene 5-oxide (SSO) by MoO(5)HMPT has been stud ied in 1,2-dichloroethane at 40 degrees C. Under conditions of excess substrate over the oxidant, three products are formed, i.e., two isome ric cis and trans bissulfoxides (SOSO) and sulfide-sulfone (SSO2) whic h quantitatively account for the active oxygen of MoO(5)HMPT consumed. The rates of appearance of the products at different reactant concent rations have been measured. A second-order rate law has been establish ed. The ratios of the rate constants and of the final concentrations o f the three products, i.e., k(2)(cis-SOSO):k(2)(trans-SOSO):k(2)(SSO2) = 1.0:4.0:1.0; (infinity):[trans-SOSO](infinity):[SSO2](infinity) = 1 .0:4.5:1.2, are in good agreement. The trans-SOSO-forming reaction is only 4-fold faster than that leading to SSO2. cis-SOSO and SSO2 are pr oduced at almost the same rate. Evidence is presented that all the oxi dation reactions are electrophilic processes taking place via a simple bimolecular mechanism not involving the coordination of the substrate to the metal. The low selectivity is due to the scarce reactivity of the thioether center in thianthrene 5-oxide. The investigation of the oxidative behavior of structurally related compounds reveals that such a low reactivity results from a combination of stereoelectronic effec ts. These findings provide a rationale to some ambiguous results obtai ned when thianthrene 5-oxide is employed as a mechanistic probe of the electronic character of the oxidants.