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Investigation of the photo-rearrangement of o-nitrobenzylesters by time-resolved resonance Raman spectroscopy

✍ Scribed by S. Schneider; M. Fink; R. Bug; H. Schupp


Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
637 KB
Volume
55
Category
Article
ISSN
1010-6030

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✦ Synopsis


The formation of the primary photoproduct (the nitronic acid) in the photo-rearrangement of o-nitrobenzylesters was investigated by time-resolved resonance Raman (lR3) spectroscopy in a polar, aprotic and polar, protic solvent. In acetonitrile, only nitronic acid is formed with a lifetime of 80 ps, whereas in methanol the nitronic acid occurs in thermal equilibrium with the nitronate anion, which has a lifetime of 100 us,


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