Electron capture ionization is the ionization of a gas phase atom or molecule by attachment of an electron to create an ion of the form A–•. The reaction is :

where the M over the arrow denotes that to conserve energy and momentum a third body is required (the molecularity of the reaction is three).

Electron capture can be used in conjunction with chemical ionization.[1]

Electron-capture mass spectrometry

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Electron-capture mass spectrometry is a type of mass spectrometry that uses electron capture ionization to form negative ions from chemical compounds with positive electron affinities. The approach is particularly effective for electrophiles. In contrast to electron ionization, EC-MS uses low energy electrons in a gas discharge. [2] EC-MS will cause less fragmentation of molecules compared to electron ionization. [3]

Negative ion formation

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  • Resonance electron capture[3]: This is also known as nondissociative EC. The compound attaches an electron to form a radical anion.[4] The energy of the electrons are about 0 eV. After the molecule captures the electron, the complex formed can stabilize during collisions and produce a stable anion that can be detected in a mass spectrometer. [3]
 
  • Dissociative resonance capture[3]: The compound fragments resulting in electron capture dissociation (ECD).[4] ECD forms an anion fragment and a radical fragment. The energy of the electrons are from 0-15 eV, but the optimum energy can vary depending on the compound.[3]
 


Fragmentation in ECI has been studied by tandem mass spectrometry.[5]

A chemical ionization source can be used in EC-MS at 1 torr.

Calibration of the mass spectrometer is important in electron capture ionization mode. A calibration compound is needed to to ensure reproducibility in EC-MS. It is used to ensure that the mass scale used is correct and that the groups of ions are constant on a regular basis.[3]

Gas chromatography electron capture MS

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Electron-capture fourier transform MS

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Particle beam electron-capture-MS

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Laser-induced electron-capture MS

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HPLC–atmospheric pressure chemical ionization MS

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Sample preparation

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  • Sample cleanup
  • Derivatization
  • Chemical transformation
  • Release tags

Instrumentation

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Electron capture detector

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Diagram of a gas chromatograph coupled to an electron capture detector [6]

An electron capture detector most often uses a radioactive source to generate electrons used for ionization. Some examples of radioactive isotopes used are 3H, 63Ni, 85Kr, and 90Sr. The gas in the detector chamber gets ionized by the radiation particles. Nitrogen, argon and helium are common carrier gases used in the ECD. Argon and helium need to be combined with another gas, such as methane, in order to prevent immediate conversion into metastable ions. The combination will extend the lifetime of the metastable ions (10-6 seconds). The methane will cool the electrons during the collisions. [7] The addition of methane will enhance the ability to form negative ions under high pressure because it will adjust the thermal energy to be similar to the energy distribution of the ions. Methane is the most common gas used because it can produce many positive ions when it collides with electrons. These positive ions will then form low energy electrons used for ionization:

 [3]

An ECD is used in some gas chromatography systems.[8]







Applications

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EC-MS has been used for identifying trace levels of chlorinated contaminants in the environment such as polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs), and other polychlorinated compounds. Pesticide derivatives, nitrogen containing herbicides, and phosphorus-containing insectides have also been detected in EC-MS. [3]

Bile acids can detected in various body fluids by using GC-EC-MS. Oxidative damage can also be monitored in trace amounts by analyzing oxidized phenylalanine using GC-EC-MS.[4]


Advantages

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EC-MS is a sensitive ionization method. Forming negative ions through electron capture ionization is more sensitive than forming positive ions through chemical ionization.[1]

It is a selective ionization technique that can prevent the formation of common matrices found in environmental contaminants during ionization. Electron capture ionization will have less interference from these matrices compared to electron ionization.

Electron capture mass spectra can distinguish between certain isomers that EI-MS cannot.[3]

Limitations

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Different energies in the ion source can cause a variation in mechanisms of negative ion formation and make the mass spectra hard to duplicate. Results shown in the mass spectrum can vary from instrument to instrument.

The temperature of the ion source needs to be monitored. An increase in fragment ions occurs at higher temperatures. Lower temperatures will lower the energy of electrons. Temperatures can vary, but it is important for electron energy to approach thermal levels for resonance electron capture to occur.

Pressure of the added enhancement gas needs to be determined. Increasing the pressure will help stabilize the anions and extend the lifetimes of the negative ions. If the pressure is too high, not as many ions can exit the ion source.

Analysis should be done using low sample loads for GC-EC-MS. The amount of sample will affect the ion abundance and cause variations in data. [3]

See also

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Electron capture dissociation

References

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  1. ^ a b Donald F. Hunt; Frank W. Crow (1978), "Electron capture negative ion chemical ionization mass spectrometry", Analytical Chemistry, 50 (13): 1781, doi:10.1021/ac50035a017{{citation}}: CS1 maint: multiple names: authors list (link)
  2. ^ Leis HJ, Fauler G, Rechberger GN, Windischhofer W (June 2004). "Electron-capture mass spectrometry: a powerful tool in biomedical trace level analysis". Curr. Med. Chem. 11 (12): 1585–94. doi:10.2174/0929867043365035. PMID 15180565.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ a b c d e f g h i j Ong, Voon S.; Hites, Ronald A. (1994). "Electron capture mass spectrometry of organic environmental contaminants". Mass Spectrometry Reviews. 13 (3): 259–283. doi:10.1002/mas.1280130305. ISSN 0277-7037.
  4. ^ a b c Giese, RW (2000). "Electron–capture mass spectrometry: recent advances". Journal of Chromatography. 892 (1–2): 329–346. doi:10.1016/S0021-9673(00)00364-2. PMID 11045497.
  5. ^ Wei J, Liu S, Fedoreyev SA, Voinov VG (2000). "A study of resonance electron capture ionization on a quadrupole tandem mass spectrometer". Rapid Commun. Mass Spectrom. 14 (18): 1689–94. doi:10.1002/1097-0231(20000930)14:18<1689::AID-RCM75>3.0.CO;2-G. PMID 10962492.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ http://www.esrl.noaa.gov/gmd/hats/insitu/insitu.html
  7. ^ Pellizzari, E. D. (1974). "Electron capture detection in gas chromatography". Journal of Chromatography A. 98 (2): 323. doi:10.1016/S0021-9673(00)92077-6.
  8. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "electron capture detector (in gas chromatography)". doi:10.1351/goldbook.E01981

Possible References

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[1] [2] [3] [4] [5] [6] [7] [8]

References

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  1. ^ Ma, Yuning; Hites, Ronald A. (2013). "Electron impact, electron capture negative ionization and positive chemical ionization mass spectra of organophosphorus flame retardants and plasticizers". Journal of Mass Spectrometry. 48 (8): 931–936. doi:10.1002/jms.3235. ISSN 1076-5174.
  2. ^ Reth, Margot; Oehme, Michael (2004). "Limitations of low resolution mass spectrometry in the electron capture negative ionization mode for the analysis of short- and medium-chain chlorinated paraffins". Analytical and Bioanalytical Chemistry. 378 (7): 1741–1747. doi:10.1007/s00216-004-2546-9. ISSN 1618-2642.
  3. ^ Compton, R. N. (1966). "Nondissociative Electron Capture in Complex Molecules and Negative-Ion Lifetimes". The Journal of Chemical Physics. 45 (12): 4634. doi:10.1063/1.1727547. ISSN 0021-9606.
  4. ^ Zubarev, Roman A (2004). "Electron-capture dissociation tandem mass spectrometry". Current Opinion in Biotechnology. 15 (1): 12–16. doi:10.1016/j.copbio.2003.12.002. ISSN 0958-1669.
  5. ^ Rosenfelder, Natalie; Vetter, Walter (2009). "Gas chromatography coupled to electron capture negative ion mass spectrometry with nitrogen as the reagent gas - an alternative method for the determination of polybrominated compounds". Rapid Communications in Mass Spectrometry. 23 (23): 3807–3812. doi:10.1002/rcm.4327. ISSN 0951-4198.
  6. ^ A. Zlatkis; C.F. Poole (1 January 1981). Electron Capture: Theory and Practice in Chromatography. Elsevier. pp. 359–. ISBN 978-0-08-085821-0.
  7. ^ Chhabil Dass (11 May 2007). Fundamentals of Contemporary Mass Spectrometry. John Wiley & Sons. ISBN 978-0-470-11848-1.
  8. ^ Ong, Voon S.; Hites, Ronald A. (1994). "Electron capture mass spectrometry of organic environmental contaminants". Mass Spectrometry Reviews. 13 (3): 259–283. doi:10.1002/mas.1280130305. ISSN 0277-7037.

Possible Revisions

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  • Contents: Section for resonance electron capture and dissociative electron capture
  • Overview how this is a Negative-Ion Chemical Ionization
  • Expand on electron capture ionization coupled to Gas Chromatography
  • Expand on electron capture detectors
  • Expand on electron capture mass spectrometry