The radical cations of bicyclo[3.2.0]hepta-2,6-diene and bicyclo[3.2.0]hept-2-ene have been obtained by γ-irradiation of the parent compounds in Freon matrices and their structures investigated by EPR spectroscopy and MNDO and INDO calculations. In a CFCl3 matrix, ring opening to the isomeric cycloheptatriene and cycloheptadiene radical cations occurred, whereas in a CF2ClCFCl2 matrix the prevalent reaction was deprotonation to the neutral bicyclo[3.2.0]hepta-2,6-dien-4-yl and bicyclo[3.2.0]hept-2-en-4-yl radicals, respectively.

Matrix isolation EPR study of novel radical cations from bicyclic[3.2.0] and monocyclic C7H8 and C7H10 compounds

FAUCITANO, ANTONIO;BUTTAFAVA, ARMANDO;MARTINOTTI, FAUSTA;
1992-01-01

Abstract

The radical cations of bicyclo[3.2.0]hepta-2,6-diene and bicyclo[3.2.0]hept-2-ene have been obtained by γ-irradiation of the parent compounds in Freon matrices and their structures investigated by EPR spectroscopy and MNDO and INDO calculations. In a CFCl3 matrix, ring opening to the isomeric cycloheptatriene and cycloheptadiene radical cations occurred, whereas in a CF2ClCFCl2 matrix the prevalent reaction was deprotonation to the neutral bicyclo[3.2.0]hepta-2,6-dien-4-yl and bicyclo[3.2.0]hept-2-en-4-yl radicals, respectively.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/468836
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