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- Publisher
- Wiley
- Copyright
- Copyright © 2011 Wiley Subscription Services, Inc., A Wiley Company
- ISSN
- 1001-604X
- eISSN
- 1614-7065
- DOI
- 10.1002/cjoc.201180253
- Publisher site
- See Article on Publisher Site
Abstract
A DFT calculations are carried out at UB3LYP/6‐311++G (3df, 2p) levels of theory to study electrocyclic thermal cleavage of four (R) derivatives of unsaturated bicyclic diaziridines, 1X‐R, to produce corresponding (Z) and (E) azomethine imides (2X‐Z, 2X‐E, 3X‐Z and 3X‐E), where X=H, Me, t‐Bu and Ph. Cleavage of 1X‐R series to form the most stable 3X‐Z product, (path 2) is found the favored procedure because of delocalized negative charge on five atoms and lower steric effect in related transition state. According to IRC calculations in paths 1 and 2, C6N1 bond is cleaved before the rate determinating step (transition state). The stability of unsaturated bicyclic diaziridines and their corresponding (Z) and (E) azomethine imides is in the following order in gas phase and chloroform, tetrahydrofuran, and acetone solvents: 3X‐Z<3X‐E<2X‐Z<2X‐E<1X‐R<1X‐S.
Journal
Chinese Journal of Chemistry – Wiley
Published: Jul 1, 2011
Keywords: ; ; ; ; ;