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Charge‐state distributuion and electric‐discharge suppression in negative‐ion electrospray mass spectrometry using/chlorinated solvents
Author(s) -
Cole Richard B.,
Harrata A. Kamel
Publication year - 1992
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.1290060811
Subject(s) - chemistry , solvation , solvent , electrospray , chlorine , mass spectrometry , ion , ion mobility spectrometry , analytical chemistry (journal) , electrospray ionization , valence (chemistry) , chlorine atom , solvent effects , organic chemistry , chromatography , medicinal chemistry
Solvent effects in electrospray mass spectrometry performed in the negaative‐ion mode have been examined, for a series of low‐nucleophilicity chlorinated solvents. The charge‐state distribution of a test analyte was observed to change radically with the nature of the solvent. Formation of anions of higher charge stae was favored in solvents of higher polarity. The shift in the charge‐state distribution has been largely attributed to improved solvation of chaarge sites by increasingly polar solvents. Evidence suggests that valence electrons of the chlorine atoms do not contribute significantly to solvation of acidic protons. Highly chlorinated solvents in teh electrospray bath gas serve to suppress electrical (corona) discharge phenomena. The latter effect was magnified with increasing percent weight of chlorine in the solvent. The observed discharge suppression has been attributed to electron‐capture preocesses. This solvent effect was muted when a highly efficient electron seavenger(i. e., SF 6 ) comprised the elctrospray high gas.