Cycloparaphenylenes <i>via</i> [2+2+2] cycloaddition-Reference-Cited by-同舟云学术

Cycloparaphenylenes via [2+2+2] cycloaddition

Published:2022 Issue:54 Volume:58 Page:7483-7494
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kohrs Daniel¹²^ORCID,Volkmann Jannis¹²^ORCID,Wegner Hermann A.¹²^ORCID

Affiliation:

1. Institute of Organic Chemistry, Justus Liebig University Giessen, Heinrich-Buff-Ring 17, 35392 Giessen, Germany

2. Center for Material Research (ZfM/LaMa), Justus Liebig University Giessen, Heinrich-Buff-Ring 16, 35392 Giessen, Germany

Abstract

Syntheses of cycloparaphenylenes utilizing the [2+2+2] cycloaddition have been highlighted and categorized according to the function of this key reaction.

Funder

Justus Liebig Universität Gießen

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/2022/CC/D2CC02289C

Reference71 articles.

1. New advances in nanographene chemistry

2. Design and Synthesis of Carbon Nanotube Segments

3. Cycloparaphenylenes and related nanohoops

4. Carbon allotropes: beyond graphite and diamond

5. Topologically Unique Molecular Nanocarbons

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