Ervasti, H.K., Jobst, K.J., Burgers, P.C., Ruttink, P.J.A., Terlouw, J.K.
Large energy barriers prohibit the rearrangement of solitary acrylonitrile ions, CH₂=CHC≡N•+, into their more stable hydrogen-shift isomers CH₂=C=C=NH•+ or CH=CH–C=NH•+. This prompted...
Ervasti, H.K., Lee, R., Burgers, P.C., Ruttink, P.J.A., Terlouw, J.K.
The predominant dissociation process observed for metastable protonated oxalic acid ions HOOC-C(OH)2+ (generated by self-protonation) leads to H3O++CO+CO2. We have traced the mechanism of this...
Jobst, K.J., Burgers, P.C., Ruttink, P.J.A., Terlouw, J.K.
A previous study [Ch. Lifshitz, P.J.A. Ruttink, G. Schaftenaar, J.K. Terlouw, Rapid Commun. Mass Spectrom. 1 (1987) 61] shows that metastable N-hydroxyacetamide ions CH3C(=O)NHOH+ (HA-1) do not...
Lee, R., Ruttink, P.J.A., Burgers, P.C., Terlouw, J.K.
Previous studies have shown that the solitary ketene-water ion CH2=C(=O)OH2+ (1) does not isomerize into CH2=C(OH)2+ (2), its more stable hydrogen shift isomer. Tandem mass spectrometry based...
Burgers, P.C., Ruttink, P.J.A.
The barrier for the radical isomerization CH3Oo --> oCH2OH is calculated by CBS-QB3 to be 29.7 kcal mol-1 and lies higher (by 5.7 kcal mol-1) than the dissociation limit CH2O+Ho. Hence, CH3Oo does...