Stereospecific photochemistry of Δ2-1,2,3-triazolines in solution and in the solid state: scope and mechanistic studiesElectronic supplementary information (ESI) available: Synthetic and photochemical procedures, as well as IR, 1H and 13C NMR. See DOI: 10.1039/c7pp00187h

• Main Authors: Chung, Tim S, Xue, Yang, Carranza, Alberto, Garcia-Garibay, Miguel A
• Format: Journal Article
• Language: English
• Published: 13.09.2017
• ISSN: 1474-905X; 1474-9092
• DOI: 10.1039/c7pp00187h

The stereospecific photochemistry of ten N -aryl-substituted cis - or trans -Δ 2 -1,2,3-triazolines to form the corresponding cis - or trans -aziridines was investigated both in solution and in the solid-state. We found that photochemical reactions in the solid state are more stereospecific than in solution for the 8 crystalline Δ 2 -1,2,3-triazolines. Additionally, triplet sensitization for some triazolines results in triplet biradicals, which provide the more thermodynamically favored trans -aziridine regardless of the starting triazoline stereochemistry. Product analyses as a function of temperature and solvent polarity suggest that the electronic excitation of the Δ 2 -1,2,3-triazolines results in the formation of a 1,3-biradical intermediate. A simple two-step process for the synthesis of aziridines relies on the crystallization and stereospecific solid state photoreaction of triazolines obtained by dipolar cycloaddition between azides and activated alkenes.