Reactions of the trimethylsilyl ion with 1,2-cyclopentanediol isomers in the collision region of a triple quadrupole instrument
β Scribed by William J. Meyerhoffer; Maurice M. Bursey
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 678 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Various nucleophilic reagents (methanol, acetone, ammonia and trimethylamine), characterized by di β erent proton affinities, were introduced into the collision cell of the triple quadrupole as reactive gases for collisionally activated reaction (CAR) studies on stereoisomeric tetracyclic terpenes co
## Low -energy reactive collisions between the negative molecular ion of a tetrachlorodibenzo-pdioxin (TCDD) and oxygen inside the collision cell of a triple-stage quadrupole mass spectrometer produce a substitution ion IM -C1+ 01-, a phenoxide ion [C6H4-n02Clnl-', [M -HCIJ-', and CI-by which 1,2,