Why CH3CH3+· formation competes with h· loss from CCCO C3H6O+· isomers-Reference-Cited by-同舟云学术

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Why CH3CH3+· formation competes with h· loss from CCCO C3H6O+· isomers

Published:2003-02-01 Issue:2 Volume:14 Page:136-142
ISSN:1044-0305
Container-title:Journal of the American Society for Mass Spectrometry
language:en
Short-container-title:J. Am. Soc. Mass Spectrom.

Author:

Hudson Charles E.¹,McAdoo David J.¹,Griffin Lawrence L.²,Traeger John C.³

Affiliation:

1. Marine Biomedical Institute, University of Texas Medical Branch, 301 University Blvd., 77555-1043, Galveston, TX, USA

2. Department of Marine Sciences, Texas A & M University at Galveston, Galveston, Texas, USA

3. Department of Chemistry, La Trobe University, Victoria, Australia

Publisher

American Chemical Society (ACS)

Subject

Spectroscopy,Structural Biology

Link

https://pubs.acs.org/doi/pdf/10.1016/S1044-0305%2802%2900864-4

Reference34 articles.

1. Unimolecular dissociations of excited C3H6O+: A photoelectron—photoion coincidence study of cyclopropanol and allyl alcohol

2. Metastable ions characteristics. XVIII. Enolic C3H6O+ ion formed from aliphatic ketones

3. Intramolecular energy redistribution in polyatomic ions

4. A S N 2 Reaction That Avoids Its Deep Potential Energy Minimum

5. Nonstatistical Dynamics in Deep Potential Wells: A Quasiclassical Trajectory Study of Methyl Loss from the Acetone Radical Cation

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4. Photoelectron imaging of propanal by resonant multiphoton ionization via the 3s Rydberg state;Physical Chemistry Chemical Physics;2006

5. Formation of C6HnSi+ (n = 5–8) from phenylsilane: an experimental and theoretical study;International Journal of Mass Spectrometry;2004-09

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