Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/95959
Type: Artigo de periódico
Title: The Ionized Methylene Transfer From The Distonic Radical Cation +ch 2-o-ch 2 To Heterocyclic Compounds. A Pentaquadrupole Mass Spectrometric Study
Author: Gozzo F.C.
Eberlin M.N.
Abstract: Ion-molecule reactions of the mass-selected distonic radical cation +CH 2-O-CH 2 · (1) with several heterocyclic compounds have been investigated by multiple stage mass spectro- metric experiments performed in a pentaquadrupole mass spectrometer. Reactions with pyridine, 2-, 3-, and 4-ethyl, 2-methoxy, and 2-n-propyl pyridine occur mainly by transfer of CH 2 +· to the nitrogen, which yields distonic N-methylene-pyridinium radical cations. The MS 3 spectra of these products display very characteristic collision-induced dissociation chemistry, which is greatly affected by the position of the substituent in the pyridine ring. Ortho isomers undergo a δ-cleavage cyclization process induced by the free-radical character of the N-methylene group that yields bicyclic pyridinium cations. On the other hand, extensive CH 2 +· transfer followed by rapid hydrogen atom loss, that is, a net CH + transfer, occurs not to the heteroatoms, but to the aromatic ring of furan, thiophene, pyrrole, and N-methyl pyrrole. The reaction proceeds through five- to six-membered ring expansion, which yields the pyrilium, thiapyrilium, N-protonated, and N-methylated pyridine cations, respectively, as indicated by MS 3 scans. Ion 1 fails to transfer CH 2 +· to tetrahydrofuran, whereas a new α-distonic sulfur ion is formed in reactions with tetrahydrothiophene. Unstable N-methylene distonic ions, likely formed by transfer of CH 2 +· to the nitrogen of piperidine and pyrrolidine, undergo rapid fragmentation by loss of the α-NH hydrogen to yield closed-shell immonium cations. The most thermodynamically favorable products are formed in these reactions, as estimated by ab initio calculations at the MP2/6-31G(d,p)//6-31G(d,p) + ZPE level of theory. © 1995 American Society for Mass Spectrometry.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/1044-0305(95)00246-A
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0000537874&partnerID=40&md5=f43867d627acd9c5137c91cf5574ab66
Date Issue: 1995
Appears in Collections:Unicamp - Artigos e Outros Documentos

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