Substituent effect on the N-oxidation of 1,10-phenanthroline derivatives by peroxomonosulfate ion
Author:
Affiliation:
1. Department of Inorganic and Analytical Chemistry
2. University of Debrecen
3. Egyetem tér 1
4. Hungary
Abstract
Both the acidity of a series of substituted 1,10-phenanthrolines and their reactivity towardsN-oxidation are predominantly governed by electronic effects.
Funder
Országos Tudományos Kutatási Alapprogramok
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2017/NJ/C7NJ01860F
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4. In Situ Generated HypoIodite Activator for the C2 Sulfonylation of Heteroaromatic N-oxides
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1. Complexes of 1,10-phenanthroline-mono-N-oxides with copper(II) and nickel(II) in aqueous solution and solid phase;Inorganica Chimica Acta;2023-11
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3. Oxidation and Reduction;Organic Reaction Mechanisms Series;2020-07-24
4. Radical-Triggered Chemiluminescence of Phenanthroline Derivatives: An Insight into Radical–Aromatic Interaction;ACS Omega;2019-08-30
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