DFT Study on the Cycloreversion of Thietane Radical Cations

LUIS R. DOMINGO; RAÚL PÉREZ-RUIZ; JUAN E. ARGÜELLO; MIGUEL A. MIRANDA

JOURNAL OF PHYSICAL CHEMISTRY A

AMER CHEMICAL SOC

Lugar: Washington; Año: 2011 vol. 115 p. 5443 - 5443

1089-5639

he molecular mechanism of the cycloreversion (CR) of thietane radical cations has been analyzed in detail at the UB3LYP/6-31G* level of theory. Results have shown that the process takes place via a stepwise mechanism leading to alkenes and thiobenzophenone; alternatively, formal [4 + 2] cycloadducts are obtained. Thus, the CR of radical cations 1a,b.+ is initiated by C2-C3 bond breaking, giving common intermediates INa,b. At this stage, two reaction pathways are feasible involving ion molecule complexes IMCa,b (i) or radical cations 4a,b.+ (ii). Calculations support that 1a.+ follows reaction pathway ii (leading to the formal [4 + 2] cycloadducts 5a). By contrast, 1b.+ follows pathway i, leading to trans-stilbene radical cation (2b.+) and thiobenzophenone.