Isomer-Specific Heavy-Atom Tunneling in the Ring Expansion of Fluorenylazirines

• Published in: Journal of organic chemistry Vol. 88; no. 13; pp. 7893 - 7900
• Main Authors: Rowen, Julien F., Beyer, Frederike, Schleif, Tim, Sander, Wolfram
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 07-07-2023
• Subjects: Imines; Isomerism; Photolysis
• ISSN: 0022-3263; 1520-6904
• DOI: 10.1021/acs.joc.3c00484

The photolysis of 2-azidofluorene in solid argon at 3 K results in the formation of 2-fluorenylnitrene. The nitrene undergoes subsequent rearrangements to two isomeric didehydroazepines (ketenimines) which differ in the position of the N atom in the seven-membered ring. The rearrangement of the nitrene to the didehydroazepines proceeds in a two-step process. The first step is a photochemical rearrangement to form the corresponding isomeric benzazirines A and B. The second step is the opening of the three-membered rings of A and B to form the isomeric didehydroazepines. While benzazirine A could easily be detected, isomer B was not observed, despite the corresponding didehydroazepine being formed in the matrix. Further experiments revealed that A rearranges to the didehydroazepine via heavy-atom tunneling. Semiquantitative estimations based on DFT calculations confirm that A should undergo a tunneling rearrangement with tunneling rates on the order of the experimentally observed rates. In contrast, estimations for B suggest that for this isomer the tunneling rates should be much larger, resulting in lifetimes too short to be observable under the conditions of matrix isolation. These experiments demonstrate the influence of position isomerism on quantum tunneling rates.