Structural and Electronic Effects of Stepwise Reduction of a Tetraaryl[3]Cumulene-Reference-Cited by-同舟云学术

Structural and Electronic Effects of Stepwise Reduction of a Tetraaryl[3]Cumulene

Published:2019-01-14 Issue:7 Volume:131 Page:2045-2050
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Spisak Sarah N.¹,Bühringer Martina U.²,Wei Zheng¹,Zhou Zheng¹,Tykwinski Rik R.²³^ORCID,Petrukhina Marina A.¹^ORCID

Affiliation:

1. Department of Chemistry; University at Albany; State University of New York Albany NY 12222 USA

2. Department für Chemie und Pharmazie & Interdisciplinary Center for Molecular Materials (ICMM); Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU); Nikolaus-Fiebiger-Strasse 10 91058 Erlangen Germany

3. Department of Chemistry; University of Alberta; Edmonton Alberta T6G 2G2 Canada

Funder

National Science Foundation

Deutsche Forschungsgemeinschaft

The Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201812283/fullpdf

Reference55 articles.

1. Synthesis of the Butatriene C4 Function: Methodology and Applications

2. Synthesis of Cyano-Substituted Diaryltetracenes from Tetraaryl[3]cumulenes

3. Synthese von Cyano-substituierten Diaryltetracenen ausgehend von Tetraaryl[3]cumulenen

4. Unexpected Formation of a [4]Radialene and Dendralenes by Addition of Tetracyanoethylene to a Tetraaryl[5]cumulene

5. Unerwartete Bildung eines [4]Radialens und mehrerer Dendralene bei der Addition von Tetracyanoethylen an ein Tetraaryl[5]cumulen

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bending a Cumulene with Electrons: Stepwise Chemical Reduction and Structural Study of a Tetraaryl[4]Cumulene;Chemistry – A European Journal;2024-03-20

2. Repercussions of multi-electron uptake by a twistacene: a reduction-induced double dehydrogenative annulation;Organic Chemistry Frontiers;2023

3. Stepwise Generation of Mono‐, Di‐, and Triply‐Reduced Warped Nanographenes: Charge‐Dependent Aromaticity, Surface Nonequivalence, Swing Distortion, and Metal Binding Sites;Angewandte Chemie;2021-10-22

4. Stepwise Generation of Mono‐, Di‐, and Triply‐Reduced Warped Nanographenes: Charge‐Dependent Aromaticity, Surface Nonequivalence, Swing Distortion, and Metal Binding Sites;Angewandte Chemie International Edition;2021-10-22

5. Chemical Reduction of a Nanosized [6]Cyclo‐2,7‐naphthylene Macrocycle;Angewandte Chemie International Edition;2021-04-08