A THEORETICAL-STUDY OF A MODEL OF N-TERT-BUTYL-ALPHA-PHENYLNITRONE (PBN) AS ACTIVE OXYGEN SPECIES SCAVENGER

The reactions of nitrone-A, H2CN(O)H, as a simple model of N-tert-buty l-alpha-phenylnitrone (PEN), with O-1(2) and with acetylene were inves tigated from a quantum chemical point of view. The reactions have been found to give the corresponding 5-membered 1,3-dipolar cycloadditions by means of the ab initio calculations for the equilibrium states and for the transition states. The reaction ergodographies along the intr insic reaction coordinates (IRC) were studied, The virial theorem for a molecule on the IRC is investigated, A nitrone having phenyl group ( nitrone-B), like PEN, underwent 1,3-dipolar cycloaddition with superox ide (O-2(-)), while nitrone-A with O-2(-) did not make it.