Primary reactions in crystalline salts of tartaric acids studied by ESR spectroscopy
β Scribed by P.-O. Samskog; A. Lund; G. Nilsson; M.C.R. Symons
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 322 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Irradiated Rochellc salt and di-K-tartrate were examined by ESR spectroscopy in order to identify the primary products present at 71 I(. For the deuterated RocheL!~ nit we have suggested a deny scheme for a primary species thought to be the oxidation product (~3-O~CCHODCHODCO,(NtfZ On the basis of the 13C, 'Ii and 23BIa hyperfine couplings, the extra proton coupling seen in protonated Rochelle salt and data from di-K-tartrate we have reinterpreted our edier asr&urent of the 77 Ii spectrum. The new results indicate that the primary product seen at 77 R is the reduction product (K")-O~CCHODCHO~02D-(Na*) v.hich decomposes by water elimination to -02CCHO&HCO~.
There is no detectable coupIing to I? in di-tC-tartnte-
π SIMILAR VOLUMES
Molecular order and dynamics of chlorophyll a triplets in liquid crystals are studied by transient ESR following pulsed laser excitation. The time evolution of the transverse magnetization is monitored at various static and microwave magnetic fields. Analysis ofthc ESR transients isachicved by emplo