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The reaction of spiro[indoline-naphthopyrans] with nitrose oxides. Not a case of biradical double trapping. (Articolo in rivista)
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- The reaction of spiro[indoline-naphthopyrans] with nitrose oxides. Not a case of biradical double trapping. (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Alternative label
Angelo Alberti, Paola Astolfi, Mylène Campredon, Lucedio Greci, Maurizio Guerra, Dante Macciantelli, Elena Plescia (2010)
The reaction of spiro[indoline-naphthopyrans] with nitrose oxides. Not a case of biradical double trapping.
in Magnetic resonance in chemistry (Print)
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- Angelo Alberti, Paola Astolfi, Mylène Campredon, Lucedio Greci, Maurizio Guerra, Dante Macciantelli, Elena Plescia (literal)
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- ISI Web of Science (WOS) (literal)
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- ISOF-CNR, Bologna, Italy; Aix-Marseille Universisté, Marseille, France; Università Politecnica delle Marche, Ancona, Italy (literal)
- Titolo
- The reaction of spiro[indoline-naphthopyrans] with nitrose oxides. Not a case of biradical double trapping. (literal)
- Abstract
- The reactions of six differently substituted photochromic spiro[indoline-naphtopyrans] with NO or NO2 under normal daylight conditions have been investigated by means of EPR spectroscopy along with those of three structurally related spiro[indoline-benzopyrans]. The spectra due to cyclic oxynitroxides originating from double trapping of biradicals by NO were observed with the three latter derivatives, this finding being in agreement with previous results. Similar signals were also observed with the six former compounds, but in this case they were responsible for just a minor component of the spectra, the main spectral signals being due to hitherto unreported paramagnetic species that on the basis of their spectral parameters are identified as iminoxy radicals. DFT calculations at the B3LYP/6-31G* level carried out on a variety of radicals support this assignment. (literal)
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