Dithieno[ a , e ]pentalenes: Highly Antiaromatic Yet Stable π‐Electron Systems without Bulky Substituents-Reference-Cited by-同舟云学术

Dithieno[ a , e ]pentalenes: Highly Antiaromatic Yet Stable π‐Electron Systems without Bulky Substituents

Published:2020-11-23 Issue:5 Volume:27 Page:1638-1647
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Usuba Junichi¹²,Hayakawa Masahiro¹²^ORCID,Yamaguchi Shigehiro²³^ORCID,Fukazawa Aiko¹³^ORCID

Affiliation:

1. Institute for Integrated Cell-Material Sciences (WPI-iCeMS) Institute for Advanced Study Kyoto University Yoshida Sakyo-ku Kyoto 606–8501 Japan

2. Department of Chemistry Graduate School of Science and Integrated Research Consortium on, Chemical Sciences (IRCCS) Nagoya University, Furo Chikusa Nagoya 464–8602 Japan

3. Institute of Transformative Bio-Molecules (WPI-ITbM) Nagoya University Furo, Chikusa Nagoya 464–8602 Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004244

Reference129 articles.

2. Paratropicity and antiaromaticity: role of the homo-lumo energy gap

4. The potential surfaces for the lowest singlet and triplet states of cyclobutadiene

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