An Anomalous Antiaromaticity That Arises from the Cycloheptatrienyl Anion Equivalent-Reference-Cited by-同舟云学术

An Anomalous Antiaromaticity That Arises from the Cycloheptatrienyl Anion Equivalent

Published:2018-06-27 Issue:33 Volume:2018 Page:4508-4511
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Uehara Keiji¹,Mei Peifeng¹,Murayama Tomohisa¹,Tani Fumito²^ORCID,Hayashi Hironobu¹^ORCID,Suzuki Mitsuharu¹^ORCID,Aratani Naoki¹^ORCID,Yamada Hiroko¹^ORCID

Affiliation:

1. Division of Materials Science Nara Institute of Science and Technology (NAIST) 8916‐5 Tkayama‐cho 630‐0192 Ikoma, Nara Japan

2. Institute for Materials Chemistry and Engineering Kyushu University 744 Motooka, Nishi‐ku 819‐0395 Fukuoka Japan

Funder

Japan Society for the Promotion of Science

Core Research for Evolutional Science and Technology

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.201800769

Reference31 articles.

1. An Azulene‐Fused Tetracene Diimide with a Small HOMO–LUMO Gap

2. Terazulene: A High-Performance n-Type Organic Field-Effect Transistor Based on Molecular Orbital Distribution Control

3. Terazulene Isomers: Polarity Change of OFETs through Molecular Orbital Distribution Contrast

4. Preparation and Stille cross-coupling reaction of the first organotin reagents of azulenes. An efficient Pd(0)-catalyzed synthesis of 6-aryl- and biazulenes

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