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Reactions of Cation Radicals of EE Systems. 5. Acid-Base Equilibria in Nucleophilic Reactions of Pyridine and Water with Thianthrene Cation Radical
John F. Evans, Henry N. Blount
Chemistry & Biochemistry
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Article
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peer-review
38
Scopus citations
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Dive into the research topics of 'Reactions of Cation Radicals of EE Systems. 5. Acid-Base Equilibria in Nucleophilic Reactions of Pyridine and Water with Thianthrene Cation Radical'. Together they form a unique fingerprint.
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Keyphrases
Pyridine
100%
Radical Cation
100%
Nucleophilic Reaction
100%
Acid-base Equilibrium
100%
Thianthrene
100%
Nucleophile
66%
Rate-determining Step
33%
Oxides
16%
Electron Transfer
16%
Relative Stability
16%
Oxidized Form
16%
Acetonitrile
16%
Stopped Flow
16%
Adduct Formation
16%
Deprotonation
16%
Protic
16%
Aprotic
16%
Reducing Agent
16%
Deprotonated
16%
Nucleophilic Attack
16%
Regeneration Scheme
16%
Sulfur Sites
16%
Chemistry
Radical Cation
100%
Nucleophilic Reaction
100%
Acid Base Equilibrium
100%
Thianthrene
100%
Nucleophile
66%
formation
33%
Deprotonation
16%
Reducing Agent
16%
Acetonitrile
16%
Electron Transport
16%
stability
16%
Pharmacology, Toxicology and Pharmaceutical Science
Nucleophile
100%
Base
100%
Sulfur
25%
Acetonitrile
25%
Reducing Agent
25%
Oxidizing Agent
25%