Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/73690
Type: Artigo de periódico
Title: The generation, stability, dissociation and ion molecule chemistry of sulfinyl cations in the gas phase
Author: Gozzo, FC
Sorrilha, AEPM
Eberlin, MN
Abstract: Sulfinyl cations [R-S+-O (R = CH3, Ph, Cl, CH3O and C2H5O)] have been demonstrated by MO calculations in conjunction with pentaquadrupole multidimensional (2D and 3D) MS(2) and MS(3) mass spectrometric experiments to be stable and easily accessible gas phase species, and their dissociation and ion/molecule chemistry have been studied. Potential energy surface diagrams indicate that the sulfoxides (CH3)(2)S=O, Ph(2)S=O, Cl2S=O, (CH3O)(2)S=O and (C2H5O)(2)S=O do not undergo rearrangement upon dissociative ionization, yielding the corresponding sulfinyl cations as primary fragments, Ph(CH3)S=O-+., on the other hand, is predicted to isomerize to CH3-S-O-Ph(+.) via a four-membered ring transition state, yielding upon further CH3. loss the isomeric ion S=O+-Ph. The sulfinyl cations were found by ab initio calculations to be much more stable than their S=O+-R isomers, hence isomerization via [1,2-R] shifts is not expected, Direct cleavage of the R-SO+ bonds and/or processes that are preceded by isomerization dominate the low-energy collision dissociation chemistry of the sulfinyl cations, thus providing limited structural information. On the other hand, a general and structurally diagnostic ion/molecule reaction with 2-methyl-1,3-dioxolane occurs for all the sulfinyl cations yielding abundant net oxirane (C2H4O) addition products. The reaction probably occurs via a transketalization-like mechanism that leads to cyclic 2-thia-1,3-dioxolanylium ions. This reactivity parallels that of several acylium (R-C+=O) and thioacylium ions (R-C+=S), and is not shared by the isomeric ions SO+-Ph and CH2=S+-OH. While the corresponding acylium ions react extensively with isoprene by [4 + 2(+)] cycloaddition, only the phenylsulfinyl cation Ph-S+=O yields an abundant cycloadduct.
Country: Inglaterra
Editor: Royal Soc Chemistry
Rights: aberto
Identifier DOI: 10.1039/p29960000587
Date Issue: 1996
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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