Tetramerization of BEB-Doped Phenalenyls to Obtain (BE)<sub>8</sub>-[16]Annulenes (E = N, O)-Reference-Cited by-同舟云学术

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Tetramerization of BEB-Doped Phenalenyls to Obtain (BE)₈-[16]Annulenes (E = N, O)

Published:2024-04-18 Issue:17 Volume:146 Page:12100-12112
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Scholz Alexander S.¹,Bolte Michael¹,Virovets Alexander¹^ORCID,Peresypkina Eugenia¹^ORCID,Lerner Hans-Wolfram¹^ORCID,Anstöter Cate S.²^ORCID,Wagner Matthias¹^ORCID

Affiliation:

1. Institut für Anorganische und Analytische Chemie, Goethe-Universität Frankfurt am Main, Max-von-Laue-Straße 7, 60438 Frankfurt am Main, Germany

2. EaStCHEM School of Chemistry, University of Edinburgh, EH8 9YLEdinburgh,U.K.

Funder

University of Edinburgh

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.4c02163

Reference101 articles.

1. Substituted Polyacetylenes: Synthesis, Properties, and Functions

2. Synthesis of electrically conducting organic polymers: halogen derivatives of polyacetylene, (CH) x

3. Nobel Lecture: Semiconducting and metallic polymers: The fourth generation of polymeric materials

4. Annulenes, 1980–2000

5. Baumgartner, T.; Jäkle, F., Eds. Main Group Strategies towards Functional Hybrid Materials; John Wiley & Sons, Ltd.: Chichester, U.K., 2017, pp. 1–110.

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1. Hybrid materials comprising ferrocene and diaminoborane moieties: linear concatenation versus macrocyclization;Chemical Communications;2024

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