Oxidation of a Dithieno[3,4-b:3',4'-d]thiophene Cyclic Dimer Containing a Planar Cyclooctatetraene Ring: Retention of High Antiaromaticity During Reactions.

DFT calculations antiaromaticity nucleus-independent chemical shifts oxidation thiophenes

Journal

ChemPlusChem
ISSN: 2192-6506
Titre abrégé: Chempluschem
Pays: Germany
ID NLM: 101580948

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 01 02 2019
revised: 15 03 2019
entrez: 17 1 2020
pubmed: 17 1 2020
medline: 17 1 2020
Statut: ppublish

Résumé

One-electron and peracid oxidations of dithieno[3,4-b : 3',4'-d]thiophene cyclic dimer, which contains an antiaromatic planar cyclooctatetraene (COT) core, were conducted. The reaction of the cyclic dimer with SbCl

Identifiants

pubmed: 31944031
doi: 10.1002/cplu.201900064
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

704-711

Subventions

Organisme : Prof. Kotohiro Nomura (Tokyo Metropolitan University)
Organisme : JSPS KAKENHI
ID : JP17 K05977

Informations de copyright

© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Auteurs

Hinako Hamaoka (H)

Department of Chemistry Graduate School of Science, Tokyo Metropolitan University Hachioji, Tokyo, 192-0397, Japan.

Shun Shiroma (S)

Department of Chemistry Graduate School of Science, Tokyo Metropolitan University Hachioji, Tokyo, 192-0397, Japan.

Kazuaki Aburaya (K)

Rigaku Corporation 3-9-12 Matsubara-cho, Akishima, Tokyo, 196-8666, Japan.

Masashi Hasegawa (M)

Department of Chemistry Graduate School of Science, Kitasato University 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa, 252-0373, Japan.

Tohru Nishinaga (T)

Department of Chemistry Graduate School of Science, Tokyo Metropolitan University Hachioji, Tokyo, 192-0397, Japan.

Classifications MeSH