Trapping of the putative 1,2-dinitrosoarene intermediate of benzofuroxan tautomerization by coordination at ruthenium and exploration of its redox non-innocence-Reference-Cited by-同舟云学术

Trapping of the putative 1,2-dinitrosoarene intermediate of benzofuroxan tautomerization by coordination at ruthenium and exploration of its redox non-innocence

Published:2014 Issue:10 Volume:5 Page:3883-3887
ISSN:2041-6520
Container-title:Chem. Sci.
language:en
Short-container-title:Chem. Sci.

Author:

Chan Siu-Chung¹²³,England Jason⁴⁵,Wieghardt Karl⁴⁵,Wong Chun-Yuen¹²³

Affiliation:

1. Department of Biology and Chemistry

2. City University of Hong Kong

3. Kowloon, People's Republic of China

4. Max-Planck-Institut für Chemische EnergieKonversion

5. 45470 Mülheim an der Ruhr, Germany

Abstract

The N,N′-coordinated 1,2-dinitrosoarenes represent a new class of redox-active bidentate ligand.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/SC/C4SC01185F

Reference48 articles.

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3. H. Cerecetto and M.González, Benzofuroxan and Furoxan. Chemistry and Biology, Top. Heterocycl. Chem., Bioactive Heterocycle IV, Springer, Berlin/Heidelberg, 2007, vol. 10, 265–308

4. Nitric Oxide Donors: Chemical Activities and Biological Applications

5. The Properties and the Use of Substituted Benzofuroxans in Pharmaceutical and Medicinal Chemistry: A Comprehensive Review

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