## Abstract In this communication we present the first stable zwitterionic spirocyclic Meisenheimer compound based on an N→N rearrangement in the reaction between picric acid and diisopropylcarbodiimide. The structure was confirmed by single‐crystal X‐ray diffraction. Furthermore, this compound exh
Resonance Raman investigation of meisenheimer complexes derived from 1,3,5-trinitrobenzene
✍ Scribed by P. S. Santos; N. S. Gonçalves
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 307 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0377-0486
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✦ Synopsis
The Raman spectra of Meisenheimer complexes derived from 1,3,5trinitrobenzene and proline, tryptophan, albumin and pyrrolidine were obtained. The spectra excited in and out of resonance with the electronic transition at ca. 460 nm show an outstanding enhancement of modes involving mainly the symmetric stretching and deformation of the NO, groups. The results also indicate a marked reduction in the symmetric and asymmetric stretching frequencies, in addition to suggesting a decrease in symmetry on going from the parent nitro aromatic to the Meisenheimer complexes.
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## Abstract The kinetics and mechanism of cyclization of the anionic sigma complex obtained from the reaction of 1,3,5‐trinitrobenzene (TNB) and 1‐benzyl‐1‐(ethoxycarbonyl)‐2‐propanone (BEP) in the presence of triethylamine (NEt~3~) have been studied in CH~3~CN–CH~3~OH (50% v/v). The order of the r
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