Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/81294
Type: Artigo de periódico
Title: Locating the charge site in heteroaromatic cations
Author: Carvalho, M
Gozzo, FC
Mendes, MA
Sparrapan, R
Kascheres, C
Eberlin, MN
Abstract: Low-energy collision-induced dissociation (CID) and ion-molecule reactions with 2-methyl-1,3-dioxolane (MD) performed by pentaquadrupole (QqQqQ) mass spectrometry were applied to locate the charge site in isomeric heteroaromatic cations. The 2-, 3-, and 4-pyridyl cations are indistinguishable by CID. However, as suggest ed by MS3 experiments and ab initio calculations, the 2-pyridyl cation reacts extensively with MD by a transacetalization-like mechanism to afford a bicyclic dihydrooxazolopyridyl cation. The 3- and 4-pyridyl cations, on the contrary react predominantly with MD by proton transfer, as does the analogous phenyl cation. The 2-. 4-, and 5-pyrimidyl cations display characteristic CID behavior. In addition, the 2-pyrimidyl cation reacts extensively with MD by the transacetalization-like mechanism, whereas proton transfer occurs predominantly for the 4- and 5-pyrimidyl cations. The ions thought to be the 2- and 3-furanyl and 2- and 3-thiophenyl cations show indistinguishable CID and ion-molecule behavior. This is most likely the result of their inherent instability in the gas phase and their spontaneous isomerization to the corresponding butynoyl and butynethioyl cations HC=CHCH2C=O+ and HC=CHCH2C=S+. These isomerizations, which are considerably exothermic according to G2(MP2) ab initio calculations, are indicated by a series of experimental results. The ions dissociate upon CID by loss of CO or CS and undergo transacetalization with MD. Most informative is the participation of HC=CHCH2C=S+ in a transacetalization/dissociation sequence with replacement of sulfur by oxygen, which is structurally diagnostic for thioacylium ions. It is therefore possible to locate the charge site of the 2-pyridyl and the three 2-, 4-, and 5-pyrimidyl cations and to identify the isomeric precursors from which they are derived. However, rapid isomerization to the common HC=CHCH2-C=O(S)(+) ion eliminates characteristic chemical behavior that could result from different charge locations in the heteroaromatic 2- and 3-furanyl and 2- and 3-thiophenyl cations.
Subject: ab initio calculations
collision-induced dissociation
in-molecule reactions
mass spectrometry
Country: Alemanha
Editor: Wiley-v C H Verlag Gmbh
Rights: fechado
Identifier DOI: 10.1002/(SICI)1521-3765(19980710)4:7<1161
Date Issue: 1998
Appears in Collections:Unicamp - Artigos e Outros Documentos

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