Biradicaloids Based on Ladder-Type Quinoidal Phyenylenevinylenes
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- ZHU Xiaozhang
- Univ of Tokyo
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- TSUJI Hayato
- Univ of Tokyo
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- NAKAMURA Eiichi
- Univ of Tokyo
Bibliographic Information
- Other Title
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- ラダー型フェニレンビニレン骨格を有するキノイド化合物の合成と物性
Abstract
Ladder-type quinoidal molecules of carbon-bridged phenylenevinylenes were designed and synthesized. The novel biradical nature was confirmed by ESR and SQUID measurements and further elucidated by theoretical calculations. Compared to the corresponding aromatic precursors, the band gaps of the compounds remarkably decreased, which are in agreement with the biradical feature. Significantly high stability was observed in solid and solution states, which can be ascribed to the anti-oxidation ability due to deep HOMO levels confirmed by DPV measurements. Unexpectedly, near-infrared (NIR) emission was observed at room temperature for both compounds. Both compounds afford stable dianion species by electrochemical and chemical reduction, accompanied with emission switching behavior.
Journal
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- Abstracts of Symposium on Physical Organic Chemistry
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Abstracts of Symposium on Physical Organic Chemistry 2011 (0), 163-163, 2011
The Society of Physical Organic Chemistry, Japan
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Details 詳細情報について
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- CRID
- 1390001205554943488
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- NII Article ID
- 130004645660
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed