Calibration of linked scan spectra for tandem double-focussing mass spectrometers
β Scribed by R.K. Boyd; P.A. Bott; D.J. Harvan; J.R. Hass
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 848 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0168-1176
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A protocol for establishing standard instrument conditions for the measurement of product ion tandem mass spectra from parent ions generated by liquid secondary ion mass spectrometry (LSIMS) is presented. The ion at m/z 319 (C') from 2-butyltriphenylphosphonium bromide is selected as the parent ion
Loss of the A ring in the electron-impact mass spectra of the trimethylsilyl (TMS) derivatives of several cholesterol oxidation products is accompanied by intramolecular migration of the 3-O-TMS group to the charge-retaining portion of the molecule. Linked-scan techniques (B/E and B(2)/E) were used
A modern ion trap offers several advantages when using full scan tandem mass spectrometry (MS/MS) instead of selected-reaction monitoring (SRM); these advantages are discussed and a comparison of SRM and full scan MS/MS is made. An example of the application of full scan MS/MS to mixture analysis is