Accurate O−H Bond Dissociation Energy Differences of Hydroxylamines Determined by EPR Spectroscopy: Computational Insight into Stereoelectronic Effects on BDEs and EPR Spectral Parameters-Reference-Cited by-同舟云学术

Accurate O−H Bond Dissociation Energy Differences of Hydroxylamines Determined by EPR Spectroscopy: Computational Insight into Stereoelectronic Effects on BDEs and EPR Spectral Parameters

Published:2010-12-23 Issue:2 Volume:76 Page:631-636
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Billone Paul S.¹,Johnson Paul A.²,Lin Shuqiong³,Scaiano J. C.¹,DiLabio Gino A.²,Ingold K. U.³

Affiliation:

1. Department of Chemistry, University of Ottawa, 10 Marie Curie, Ottawa, ON, Canada K1N 6N5

2. National Institute for Nanotechnology, National Research Council of Canada, 11421 Saskatchewan Drive, Edmonton, AB, Canada T6G 2M9

3. National Research Council, 100 Sussex Drive, Ottawa, ON, Canada K1A 0R6

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo1021794

Reference28 articles.

1. Hydroxylamines as Oxidation Catalysts: Thermochemical and Kinetic Studies

2. Mechanisms of Reaction of Aminoxyl (Nitroxide), Iminoxyl, and Imidoxyl Radicals with Alkenes and Evidence that in the Presence of Lead Tetraacetate, N-Hydroxyphthalimide Reacts with Alkenes by Both Radical and Nonradical Mechanisms

3. O−H Bond Dissociation Enthalpies of Oximes: A Theoretical Assessment and Experimental Implications

4. Effects of Solvation on the Enthalpies of Reaction of tert-Butoxyl Radicals with Phenol and on the Calculated O-H Bond Strength in Phenol

5. Kinetic Solvent Effects on Hydrogen-Atom Abstractions: Reliable, Quantitative Predictions via a Single Empirical Equation1

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