Ambient mass spectrometric detection of organometallic compounds using direct analysis in real time

From National Research Council Canada

Download
  1. (PDF, 1 MB)
DOIResolve DOI: https://doi.org/10.1021/ac901778n
AuthorSearch for: 1; Search for: 1; Search for: ; Search for: ; Search for: 1ORCID identifier: https://orcid.org/0000-0002-2377-2615
Name affiliation
  1. National Research Council Canada. NRC Institute for National Measurement Standards
FormatText
TypeArticle
Journal titleAnalytical Chemistry
ISSN0003-2700
1520-6882
Volume81
Issue23
Pages9834–9839
Abstract
The present work describes the mass spectrometric detection of organometallic compounds following their atmospheric pressure ionization using a commercial direct analysis in real time (DART) ion source. Several organometallic compounds of As, Fe, Hg, Pb, Se, and Sn were examined, and their corresponding mass spectra as well as induced fragmentation patterns were recorded. Gas phase sampling of the pure organometallic compounds or their solutions prepared in toluene generated temporally stable signals. For the majority of the compounds, the molecular ion or protonated molecule was detected; noticeable exceptions are the tetra-substituted compounds for which their less-substituted species dominated. The organometallic species were used as model compounds for a systematic investigation of the impact of operating parameters of the DART source, including gas temperature and electrode voltages. In general, results have shown that powering the electrodes designed to remove ions from the DART gas stream results in a reduction in signal intensity for most of the compounds investigated, suggesting that charged species from the plasma play an important role in the ionization process of the test analytes.
Publication date
LanguageEnglish
Peer reviewedYes
NPARC number21277192
Export citationExport as RIS
Report a correctionReport a correction
Record identifierd3ffbfaa-b0b0-4654-af69-25679cb602df
Record created2016-01-05
Record modified2020-02-07
Report a problem on this page
Date modified: