Di- vs. tetra-substituted quinonediimines: a drastic effect on coordination chemistry-Reference-Cited by-同舟云学术

Di- vs. tetra-substituted quinonediimines: a drastic effect on coordination chemistry

Published:2017 Issue:38 Volume:46 Page:12794-12803
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Lavaud Lucien¹²³⁴^ORCID,Chen Zhongrui¹²³⁴,Elhabiri Mourad⁵⁶⁷⁸⁴^ORCID,Jacquemin Denis⁹¹⁰¹¹¹²⁴^ORCID,Canard Gabriel¹²³⁴^ORCID,Siri Olivier¹²³⁴^ORCID

Affiliation:

1. Aix Marseille Université

2. CNRS UMR 7325 Centre Interdisciplinaire de Nanosciences de Marseille (CINaM)

3. 13288 Marseille cedex 09

4. France

5. Equipe Chimie Bioorganique et Médicinale

6. Laboratoire de chimie Moléculaire

7. UMR 7509 CNRS-Université de Strasbourg

8. 67200 Strasbourg

9. Laboratoire CEISAM

10. UMR CNRS 6230

11. Université de Nantes

12. 44322 Nantes

Abstract

N,N′-Di-substituted benzoquinonediimine ligands behave differently in coordination chemistry compared to the well-known N,N′,N′′,N′′′-tetra-substituted analogues.

Funder

Agence Nationale de la Recherche

FP7 Ideas: European Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/DT/C7DT01884C

Reference41 articles.

1. S. Pataï and Z.Rappoport, The Chemistry of the Quinonoid Compounds, Wiley, New York, 1988, vol. 1

2. Chemistry of the Redox Series from Hexahydroxybenzene to Cyclohexanehexaone

3. Review: Hydrogen Bond and Protonation as Modifying Factors of the Quinone Reactivity

4. Quinoid systems in chemistry and pharmacology

5. Supramolecular Assemblies Based on Organometallic Quinonoid Linkers: A New Class of Coordination Networks

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