Azoxy compounds and oxadiaziridines. An ab initio study of the ring closure reactions and the cis-trans isomerizationsClick to copy article linkArticle link copied!
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This article is cited by 6 publications.
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- María V. Castillo, Jorgelina L. Pergomet, Gustavo A. Carnavale, Lilian Davies, Juan Zinczuk, Silvia Antonia Brandán. FTIR, FTRaman, UV–Visible and NMR spectroscopic studies on 3,3′,4,4′-tetrachloroazoxybenzene, an azoxybenzene derivative with toxic effects. Journal of Molecular Structure 2017, 1142 , 18-27. https://doi.org/10.1016/j.molstruc.2017.04.043
- Dina Aronzon, Eric P. Levy, Peter J. Collings, Andro Chanishvili, Guram Chilaya, Gia Petriashvili. Trans–cis isomerization of an azoxybenzene liquid crystal. Liquid Crystals 2007, 34
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- David W. Ball. New potential high-energy materials: Oxadiaziridine, N2H2O. High-level calculations. Journal of Molecular Structure: THEOCHEM 2005, 724
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- Minh‐Tho Nguyen, Jose Kaneti, Lienhard Hoesch, André S. Dreiding. Triaziridines. Part III. Triaziridine, azimine, and triazene: A SCF study of the energy and structure of N
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- Renzo Cimiraglia, Maurizio Persico, Jacopo Tomasi. Alternative paths in the ring opening of oxadiaziridine: The diimide N-oxide versus the oxodiimide rearrangement. Theoretica Chimica Acta 1978, 49
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