Stable Radical Cations and Their π-Dimers Prepared from Ethylene- and Propylene-3,4-dioxythiophene Co-oligomers: Combined Experimental and Theoretical Investigations-Reference-Cited by-同舟云学术

Stable Radical Cations and Their π-Dimers Prepared from Ethylene- and Propylene-3,4-dioxythiophene Co-oligomers: Combined Experimental and Theoretical Investigations

Published:2017-07-03 Issue:14 Volume:82 Page:7245-7253
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nishinaga Tohru¹^ORCID,Sotome Yusuke¹

Affiliation:

1. Department of Chemistry, Graduate School of Science and Engineering, Tokyo Metropolitan University, Hachioji, Tokyo 192-0397, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00816

Reference59 articles.

1. Kahlfuss, C.; Saint-Aman, E.; Bucher, C.InOrganic Redox Systems: Synthesis, Properties, and Applications;Nishinaga, T., Ed.Wiley:Hoboken. NJ, 2016; pp39–88.

2. Dimerization of Conjugated Radical Cations: An Emerging Non-Covalent Interaction for Self-Assembly

3. Pancake bonds: π-Stacked dimers of organic and light-atom radicals

4. Persistent ? radical cations: self-association and its steric control in the condensed phase

5. Radically enhanced molecular recognition

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