Non-adiabatic interactions in the symmetric ring opening process of dioxirane
- 30 April 1982
- journal article
- Published by Elsevier in Chemical Physics
- Vol. 66 (1-2) , 209-215
- https://doi.org/10.1016/0301-0104(82)88020-8
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- A multiconfigurational scf study of the transformation of methylene peroxide to dioxirane Intermediates in the ozonolysis of ethyleneChemical Physics Letters, 1981
- Ab initio UHF and UHF NO CI approaches for quasi-degenerate systems: methylene peroxide (CH2OO)Chemical Physics Letters, 1980
- Multiconfigurational SCF and Cl calculations on CH2O2. An intermediate in the ozonolysis ethyleneChemical Physics Letters, 1979
- Dioxirane. Its synthesis, microwave spectrum, structure, and dipole momentJournal of the American Chemical Society, 1978
- Mass spectrometric detection of dioxirane, H2COO, and its decomposition products, H2 and CO, from the reaction of ozone with ethyleneChemical Physics Letters, 1977
- Identification of dioxirane (H2Chemical Physics Letters, 1977
- Mechanism of ozonolysis. Ab initio study of the primary ozonide and its cleavage to the Criegee intermediateJournal of the American Chemical Society, 1976
- Infrared-matrix and microwave spectroscopy of the ethylene-ozone gas-phase reactionChemical Physics Letters, 1976
- Electronic structure of the Criegee intermediate. Ramifications for the mechanism of ozonolysisJournal of the American Chemical Society, 1975
- A theoretical study of the stability and the molecular electronic structure of methylene peroxide (CH2O2)Chemical Physics Letters, 1974