Intramolecular and Intermolecular Hydrogen Bond Formation by Some Ortho-Substituted Phenols: Some Surprising Results from an Experimental and Theoretical Investigation-Reference-Cited by-同舟云学术

Intramolecular and Intermolecular Hydrogen Bond Formation by Some Ortho-Substituted Phenols: Some Surprising Results from an Experimental and Theoretical Investigation

Published:2009-05-13 Issue:22 Volume:113 Page:6275-6288
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Litwinienko Grzegorz¹,DiLabio Gino A.¹,Mulder Peter¹,Korth Hans-Gert¹,Ingold K. U.¹

Affiliation:

1. Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland, National Institute for Nanotechnology, National Research Council of Canada, 11421 Saskatchewan Drive, Edmonton, Alberta, Canada T6G 2M9, Leiden Institute of Chemistry, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands, Institut für Organische Chemie, Universität Duisburg-Essen, D-45117 Essen, Germany, and Steacie Institute for Molecular Sciences, National Research Council of Canada, 100 Sussex Drive, Ottawa,...

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp900876q

Reference57 articles.

1. Dramatic Solvent Effects on the Absolute Rate Constants for Abstraction of the Hydroxylic Hydrogen Atom from tert-Butyl Hydroperoxide and Phenol by the Cumyloxyl Radical. The Role of Hydrogen Bonding

2. Kinetic Solvent Effects on Hydroxylic Hydrogen Atom Abstractions Are Independent of the Nature of the Abstracting Radical. Two Extreme Tests Using Vitamin E and Phenol

3. Kinetic Solvent Effects on Hydrogen Atom Abstraction from Phenol, Aniline, and Diphenylamine. The Importance of Hydrogen Bonding on Their Radical-Trapping (Antioxidant) Activities1

4. Measurement of Equilibrium Constants for Complex Formation between Phenol and Hydrogen-Bond Acceptors by Kinetic Laser Flash Photolysis1

5. Solvent Effects on the Reactivity and Free Spin Distribution of 2,2-Diphenyl-1-picrylhydrazyl Radicals1

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