Synthesis, Characterization, and Electrochemical Studies of PPh3–n(dipp)n (dipp = 2,6-Diisopropylphenyl): Steric and Electronic Effects on the Chemical and Electrochemical Oxidation of a Homologous Series of Triarylphosphines and the Reactivities of the Corresponding Phosphoniumyl Radical Cations-Reference-Cited by-同舟云学术

Synthesis, Characterization, and Electrochemical Studies of PPh3–n(dipp)n (dipp = 2,6-Diisopropylphenyl): Steric and Electronic Effects on the Chemical and Electrochemical Oxidation of a Homologous Series of Triarylphosphines and the Reactivities of the Corresponding Phosphoniumyl Radical Cations

Published:2013-07-18 Issue:30 Volume:135 Page:11205-11215
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Bullock John P.¹,Bond Alan M.²,Boeré René T.³,Gietz Twyla M.³,Roemmele Tracey L.³,Seagrave Sonja D.³,Masuda Jason D.⁴,Parvez Masood⁵

Affiliation:

1. Division of Natural Sciences & Mathematics, Bennington College, Bennington, Vermont 05201, United States

2. School of Chemistry, Monash University, Clayton, Victoria 3800, Australia

3. Department of Chemistry and Biochemistry, University of Lethbridge, Lethbridge, AB, Canada T1K3M4

4. The Maritimes Centre for Green Chemistry and the Department of Chemistry, Saint Mary’s University, Halifax, Nova Scotia, Canada B3H 3C3

5. Department of Chemistry, University of Calgary, Calgary, AB, Canada T2N1N4

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja403555d

Reference66 articles.

1. 50. Mechanism of substitution at a saturated carbon atom. Part XXXII. The rôle of steric hindrance. (Section G) magnitude of steric effects, range of occurrence of steric and polar effects, and place of the wagner rearrangement in nucleophilic substitution and elimination

2. 419. Kinetics of the reaction of alkyl and aryl compounds of the nickel group with pyridine

3. Studies in Stereochemistry. I. Steric Strains as a Factor in the Relative Stability of Some Coördination Compounds of Boron

4. Persistent carbon-centered radicals

5. Steric Control of Electron Transfer. Changeover from Outer-Sphere to Inner-Sphere Mechanisms in Arene/Quinone Redox Pairs

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