The Redox Chemistry of 4-Benzoyl-N-methylpyridinium Cations in Acetonitrile with and without Proton Donors: The Role of Hydrogen Bonding-Reference-Cited by-同舟云学术

The Redox Chemistry of 4-Benzoyl-N-methylpyridinium Cations in Acetonitrile with and without Proton Donors: The Role of Hydrogen Bonding

Published:2001-04-05 Issue:17 Volume:105 Page:3663-3674
ISSN:1520-6106
Container-title:The Journal of Physical Chemistry B
language:en
Short-container-title:J. Phys. Chem. B

Author:

Leventis Nicholas¹,Elder Ian A.¹,Gao Xuerong¹,Bohannan Eric W.¹,Sotiriou-Leventis Chariklia¹,Rawashdeh Abdel Monem M.¹,Overschmidt Travis J.¹,Gaston Kimberly R.¹

Affiliation:

1. Department of Chemistry, The University of Missouri at Rolla, 142 Schrenk Hall, Rolla, Missouri 65409-0010

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp0107199

Reference101 articles.

1. Quantitative studies in stereochemistry. Photochemistry. VII. Electrochemistry. 4. Photochemical and electrochemical bimolecular reduction of aldehydes and unsymmetrical ketones. Common stereochemistry

2. Elementry steps and the solvent effect in electrochemical reduction of acetophenone

3. Electrodimerization

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