Effect of tert-butyl groups on electronic communication between redox units in tetrathiafulvalene-tetraazapyrene triads-Reference-Cited by-同舟云学术

Effect of tert-butyl groups on electronic communication between redox units in tetrathiafulvalene-tetraazapyrene triads

Published:2021 Issue:96 Volume:57 Page:12972-12975
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhou Ping¹,Aschauer Ulrich¹^ORCID,Decurtins Silvio¹,Feurer Thomas²,Häner Robert¹^ORCID,Liu Shi-Xia¹^ORCID

Affiliation:

1. Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Freiestrasse 3, Bern CH-3012, Switzerland

2. Institute of Applied Physics, University of Bern, Sidlerstrasse 5, Bern CH-3012, Switzerland

Abstract

Electronic communication between redox units in tetrathiafulvalene-tetraazapyrene triads is unambiguously mediated by the insertion of tert-butyl groups.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CC/D1CC05671A

Reference34 articles.

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2. Annulated Heterocyclic Derivatives of 1,3,6,8-Tetraazapyrene

3. Liquid crystalline behavior of tetraaryl derivatives of benzo[c]cinnoline, tetraazapyrene, phenanthrene, and pyrene: the effect of heteroatom and substitution pattern on phase stability

4. The role of electron-attracting substituents and molecular stacking motifs in the charge transport of tetraazapyrene derivatives

5. Dual role of polyphosphoric acid-activated nitroalkanes in oxidative peri-annulations: efficient synthesis of 1,3,6,8-tetraazapyrenes

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