Heat of Formation of the tert-Butyl Radical
Author:
Affiliation:
1. Biomolecular Research Institute, Parkville, Victoria 3052, Australia, and Research School of Chemistry, Australian National University, Canberra 0200, Australia
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp9826470
Reference34 articles.
1. Rate Constants for the Reactions t-C4H9+DX→i-C4H9D+X(X = Br,I), 295T(K) < 384: Heat of Formation of the tert-Butyl Radical
2. Three methods to measure RH bond energies
3. Traeger, J. C.; Kompe, B. M. InEnergetics of Organic Free Radicals; Martino Simoes, J. A., Greenberg, A., Liebmann, J. F., Eds.; Blackie Academic & Professional: London, 1996; pp 59−107.
4. Vacuum Ultraviolet Photoelectron Spectroscopy of Transient Species: Part 8, the t-Butyl Radical
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