The study of the loss of HCN โฌrom the molecular ions of [1-13C]-, [2-"C]-and [3-13C]-indolizine shows that, if the C-3 atom is eliminated predominantly, as may be expected, the C-2 atom, and (a) carbon atom(s) of the hexagonal ring are also involved. The losses of "CCH,' and GH,' from the [M-H"CN]"
An electron impact study of HCN elimination from indole by use of 13C labelling
โ Scribed by Madeleine Corval
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 550 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
The study of the loss of HCN from the molecular ions of [2โ^13^C]indole and [3โ^13^C]indole shows that, to a good approximation, only the two carbon atoms of the pentagonal ring are involved in this fragmentation process, contrary to the behaviour of the H atoms; the Cโ2 atom is eliminated predominantly, chiefly in the ion source (85โ90%) and a little less in the metastable energy range (75โ80%). The losses of ^13^CCH~3~^ห^ and C~2~H~3~^ห^ from the [M๏ฃฟH^12^CN]^+ห^ ions of the two compounds suggest the occurrence of different structures, providing evidence for several mechanisms of HCN elimination.
๐ SIMILAR VOLUMES
## Abstract Extensive ^13^C and ^15^N labelling has shown that the molecular ions of 2โ, 3โ and 4โcyanopyridine with lifetimes up to 10^โ6^ s eliminate hydrogen cyanide originating predominantly from the ring (ห65%). Moreover, this hydrogen cyanide loss occurs after an equilibrated positional inter