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Diaryldichalcogenide radical cations

Published:2015 Issue:1 Volume:6 Page:497-504
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Mallow Ole¹²³⁴,Khanfar Monther A.⁵⁶⁷⁴⁸,Malischewski Moritz⁵⁶⁷⁴,Finke Pamela¹²³⁴,Hesse Malte¹²³⁴,Lork Enno¹²³⁴,Augenstein Timo¹⁹¹⁰⁴,Breher Frank¹⁹¹⁰⁴,Harmer Jeffrey R.¹¹¹²¹³,Vasilieva Nadezhda V.¹⁴¹⁵¹⁶¹⁷,Zibarev Andrey¹⁴¹⁵¹⁶¹⁷¹⁸,Bogomyakov Artem S.¹⁹¹⁵¹⁶¹⁷,Seppelt Konrad⁵⁶⁷⁴,Beckmann Jens¹²³⁴

Affiliation:

1. Institut für Anorganische Chemie

2. Universität Bremen

3. 28359 Bremen

4. Germany

5. Institut für Chemie und Biochemie

6. Freie Universität Berlin

7. 14195 Berlin

8. Department of Chemistry

9. Karlsruhe Institute of Technology

10. 76131 Karlsruhe

11. Centre for Advanced Imaging

12. University of Queensland

13. Australia

14. Institute of Organic Chemistry

15. Russian Academy of Sciences

16. 630090 Novosibirsk

17. Russia

18. Department of Physics

19. International Tomography Centre

Abstract

One-electron oxidation of diaryldichalcogenides is the key to the preparation of the corresponding radical cations.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/SC/C4SC02964J

Reference58 articles.

1. Triphenylmethyl, ein Fall von dreiwerthigem Kohlenstoff

2. AN INSTANCE OF TRIVALENT CARBON: TRIPHENYLMETHYL.

3. Persistent carbon-centered radicals

4. S. González-Gallardo and F.Breher, Main Group Biradicaloids, Comprehensive Inorganic Chemistry II, 2013, vol. 1, pp. 413–455

5. Stretching bonds in main group element compounds—Borderlines between biradicals and closed-shell species

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