Skip to content
2000
Volume 1, Issue 1
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

The photochemical isomerization of pyrazoles was studied using ab initio methods. The singlet excited singlet state can evolve to give the Dewar isomer and the corresponding triplet state. The latter shows a lower energy and probably can be obtained with higher efficiency. The triplet state can evolve to give the corresponding 1,2-biradical and, then, the isomerization product. The same behavior was obtained by using 1,5-dimethylpyrazole. However, 1-methyl-5-phenylpyrazole gave a different behavior. The triplet state cannot evolve to give the corresponding biradical. The isomerization product can be obtained only from the Dewar isomer.

Loading

Article metrics loading...

/content/journals/loc/10.2174/1570178043488806
2004-01-01
2025-10-05
Loading full text...

Full text loading...

/content/journals/loc/10.2174/1570178043488806
Loading

  • Article Type:
    Review Article
Keyword(s): heterocycles; isomerization; photochemistry; pyrazoles
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test