Stereochemistry, Stereodynamics, and Redox and Complexation Behaviors of 2,2′‐Diaryl‐1,1′‐Biazulenes-Reference-Cited by-同舟云学术

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Stereochemistry, Stereodynamics, and Redox and Complexation Behaviors of 2,2′‐Diaryl‐1,1′‐Biazulenes

Published:2019-07-23 Issue:11 Volume:84 Page:1659-1667
ISSN:2192-6506
Container-title:ChemPlusChem
language:en
Short-container-title:ChemPlusChem

Author:

Tsuchiya Takahiro¹^ORCID,Katsuoka Yuka¹,Yoza Kenji²^ORCID,Sato Hiroyasu³,Mazaki Yasuhiro¹

Affiliation:

1. Department of ChemistryGraduate School of ScienceKitasato University 1-15-1 Kitasato, Minami-ku Sagamihara, Kanagawa 252-0373 Japan

2. Bruker Japan 3-9 Moriya-cho, Kanagawa-ku Yokohama 221-0022 Japan

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

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cplu.201900262

Reference81 articles.

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2. Recent Advances in Isoindigo‐Inspired Organic Semiconductors

3. Immobilization Strategies for Organic Semiconducting Conjugated Polymers

4. Read between the Molecules: Computational Insights into Organic Semiconductors

5. Thermoelectric plastics: from design to synthesis, processing and structure–property relationships

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4. SOMO-HOMO level conversion in triarylmethyl-cored N-heterocyclic carbene-Au(I) complexes triggered by selecting coordination halogens;Chinese Chemical Letters;2023-12

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