TY - JOUR
T1 - A field ionization and collisionally activated dissociation/charge stripping study of some [C9H10]+˙ ions
AU - Lay, J. O.
AU - Gross, M. L.
AU - Zwinselman, J. J.
AU - Nibbering, N. M.M.
PY - 1983/1
Y1 - 1983/1
N2 - The extent of isomerization of [C9H10]+˙ ions, with lifetimes of approximately 10−11 and 10−6 s has been investigated using field ionization, collisionally activated dissociation and charge stripping techniques. The [C9H10]+˙ ions which were investigated included the molecular ions of α‐methylstyrene, β‐methylstyrene, o‐methylstyrene, m‐methylstyrene, p‐methylstyrene, indan, cyclopropylbenzene, allylbenzene and the product of water loss from 3‐phenylpropanol. The field ionization spectra of all the C9H10 hydrocarbons were different indicating that isomerization to a common ion structure had not occurred to a measurable extent for ions with lifetimes of approximately 10−11 s. Collisionally activated dissociation and charge stripping results indicated that most of the [C9H10]+˙ ions continued to maintain unique ion structures (or mixtures of structures) at ion lifetimes of 10−6 s. Possible exceptions are the [C9H10]+˙ ions from allylbenzene and cyclopropylbenzene which gave indistinguishable collisionally activated dissociation and charge stripping spectra.
AB - The extent of isomerization of [C9H10]+˙ ions, with lifetimes of approximately 10−11 and 10−6 s has been investigated using field ionization, collisionally activated dissociation and charge stripping techniques. The [C9H10]+˙ ions which were investigated included the molecular ions of α‐methylstyrene, β‐methylstyrene, o‐methylstyrene, m‐methylstyrene, p‐methylstyrene, indan, cyclopropylbenzene, allylbenzene and the product of water loss from 3‐phenylpropanol. The field ionization spectra of all the C9H10 hydrocarbons were different indicating that isomerization to a common ion structure had not occurred to a measurable extent for ions with lifetimes of approximately 10−11 s. Collisionally activated dissociation and charge stripping results indicated that most of the [C9H10]+˙ ions continued to maintain unique ion structures (or mixtures of structures) at ion lifetimes of 10−6 s. Possible exceptions are the [C9H10]+˙ ions from allylbenzene and cyclopropylbenzene which gave indistinguishable collisionally activated dissociation and charge stripping spectra.
UR - http://www.scopus.com/inward/record.url?scp=0002783715&partnerID=8YFLogxK
U2 - 10.1002/oms.1210180105
DO - 10.1002/oms.1210180105
M3 - Article
AN - SCOPUS:0002783715
SN - 0030-493X
VL - 18
SP - 16
EP - 21
JO - Organic Mass Spectrometry
JF - Organic Mass Spectrometry
IS - 1
ER -