Time-resolved EPR observation of synthetic eumelanin–superoxide radical pairs
Literature Information
Publication Date
2009-07-10
DOI
10.1039/B909568C
Impact Factor
6.222
Authors
Antonio Toffoletti, Fosca Conti, Tommaso Sandron, Alessandra Napolitano, Lucia Panzella, Marco D’Ischia
View Original
Abstract
TR-EPR spectra of UV irradiated synthetic eumelanin in equilibrium with air oxygen, reveal the formation of melanin–superoxide radical pairs and allow to determine both the electron dipolar interaction D and the exchange interaction J between the two radicals.
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Source Journal
Chemical Communications
CiteScore:
8.6
Self-citation Rate:
4.7%
Articles per Year:
2458
ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry
Recommended Compounds
![tert-Butyl N-[(2-chloropyridin-4-yl)methyl]carbamate structure](https://static.chemtradehub.com/structs/916/916210-27-0-9f95.webp "tert-Butyl N-[(2-chloropyridin-4-yl)methyl]carbamate structure")
tert-Butyl N-[(2-chloropyridin-4-yl)methyl]carbamate
CAS Number:
916210-27-0
Molecular Formula:
C11H15ClN2O2
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