Abstract
Since 1912 benzofuroxans have been believed to exhibit a molecular structure characterised by the presence of two fused rings, i. e. a benzene ring and a pentatomic heterocycle containing a N−O−N fragment wherein one of the two N atoms is involved in a further N (Formula presented.) O bond, namely benzo[1,2-c]1,2,5-oxadiazole N-oxide. In this work, quantum chemical calculation results along with vibrational spectroscopic data raise fundamental questions about the electronic structure and the molecular topology of some 4,6-dinitro-derivatives of this class of compounds. An alternative interpretation is offered corroborated by the experimental vibrational and electronic spectra.
| Original language | English |
|---|---|
| Journal | ChemPhysChem |
| DOIs | |
| Publication status | Accepted/In press - 2024 |
Keywords
- 4,6-Dinitro-Benzofuroxans
- Boulton-Katritzky
- Electronic Structure
- Molecular Topology
- Rearrangement
- Tautomerism
ASJC Scopus subject areas
- Atomic and Molecular Physics, and Optics
- Physical and Theoretical Chemistry