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Gas phase charged aggregates of bis(2‐ethylhexyl)sulfosuccinate (AOT) and divalent metal ions: first evidence of AOT solvated aggregates
Author(s) -
Giorgi Gianluca,
Pini Ivana,
Ceraulo Leopoldo,
Liveri Vincenzo Turco
Publication year - 2011
Publication title -
journal of mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 1076-5174
DOI - 10.1002/jms.1971
Subject(s) - chemistry , divalent , divalent metal , inorganic chemistry , metal , ion , phase (matter) , organic chemistry
Assembling and chelating properties of sodium bis(2‐ethylhexyl)sulfosuccinate (AOTNa) towards divalent metal ions have been investigated in the gas phase by electrospray ionization mass spectrometry. A variety of positively charged monometallated and mixed metal aggregates are formed. Interestingly, several ions contain solvent (MeOH, H 2 O) molecules and constitute the most abundant AOT cationic aggregates not containing sodium. These species are the first example of solvated AOT‐metal ion aggregates in the gas phase. By increasing the surfactant aggregation number, the abundance of solvated species becomes lower than that of unsolvated ones. Decompositions of ionic species have been studied by tandem mass spectrometry, and their stability has been determined through energy resolved mass spectrometry. In contrast with positively charged AOT‐alkaline metal ion aggregates, whose decompositions are dominated by the loss of individual surfactant molecules, AOTNa‐divalent ion aggregates mainly dissociate through the cleavage of the AOT H 2 C‐O bond followed by further intramolecular fragmentations. This finding, that is consistent with an enhanced chelation of divalent ions with AOT ‐ head groups, has been taken as an indication that such aggregates are characterized by a reverse micelle‐like organization with a ionic core formed by the metal cations interacting with the negatively charged surfactant polar heads, whereas the surfactant alkyl chains point outside. Copyright © 2011 John Wiley & Sons, Ltd.