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|Type:||Artigo de periódico|
|Title:||Ketalization of gaseous acylium ions|
|Abstract:||A novel reaction of gaseous acylium ions: ketalization with diols and analogs, has been systematically studied via pentaquadrupole MS2 and MS3 experiments and ab initio calculations. A variety of alpha,beta -diols and their amino, thiol, ether, and thioether analogs have been tested for reactivity, mechanism evaluation, site selectivity, and for the effects of alpha- and beta -interfunctional separation. As for condensed-phase ketalization of neutral carbonyl compounds followed by hydrolysis, gaseous acylium ions are chemically deactivated in the form of cyclic ionic ketals by ketalization, and are efficiently released via on-line collision-induced dissociation. Ketalization of acylium ions is shown to identify and structurally characterize alpha,beta -diols and their analogs, and to distinguish regioisomers. Diastereomers can also be distinguished, as illustrated for cis and trans 1,2-diaminocyclohexane. The MS2 and MS3 data together with O-18-labeling and ab initio calculations establish for acylium ion ketalization a mechanism of anchimeric assistance with participation of the neighboring acyl group. (C) 2001 American Society for Mass Spectrometry.|
|Editor:||Elsevier Science Inc|
|Citation:||Journal Of The American Society For Mass Spectrometry. Elsevier Science Inc, v. 12, n. 2, n. 150, n. 162, 2001.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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