Diindenothienoacene–tetrathiafulvalene redox systems-Reference-Cited by-同舟云学术

Diindenothienoacene–tetrathiafulvalene redox systems

Published:2015 Issue:61 Volume:5 Page:49748-49751
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Christensen Mikkel A.¹²³⁴,Rudebusch Gabriel E.⁵⁶⁷⁸,Parker Christian R.¹²³⁴,Andersen Cecilie Lindholm¹²³⁴,Kadziola Anders¹²³⁴,Haley Michael M.⁵⁶⁷⁸,Hammerich Ole¹²³⁴,Nielsen Mogens Brøndsted¹²³⁴

Affiliation:

1. Department of Chemistry

2. University of Copenhagen

3. DK-2100 Copenhagen Ø

4. Denmark

5. Department of Chemistry & Biochemistry and The Materials Science Institute

6. University of Oregon

7. Eugene

8. USA

Abstract

The redox properties and cation associations of extended tetrathiafulvalenes with diindenothienoacene cores are strongly dependent on the number and regioisomeric structural orientation of the central thiophene units.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA09581F

Reference17 articles.

1. Stable π-dimer of a tetrathiafulvalene cation radical encapsulated in the cavity of cucurbit[8]uril

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4. Direct Observation of Mixed-Valence and Radical Cation Dimer States of Tetrathiafulvalene in Solution at Room Temperature: Association and Dissociation of Molecular Clip Dimers Under Oxidative Control

5. Face-to-Face Dimeric Tetrathiafulvalenes and Their Cation Radical and Dication Species as Models of Mixed Valence and π-Dimer States

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