- 【Updated on May 12, 2025】 Integration of CiNii Dissertations and CiNii Books into CiNii Research
- Trial version of CiNii Research Knowledge Graph Search feature is available on CiNii Labs
- Suspension and deletion of data provided by Nikkei BP
- Regarding the recording of “Research Data” and “Evidence Data”
Synthesis of Highly Fluorescent Cationic Chlorophyll-<i>a</i> Derivatives Possessing a <i>p</i>-Aminopyridinio Group at the 31-Position
-
- Shin Ogasawara
- Graduate School of Life Sciences, Ritsumeikan University, Kusatsu, Shiga 525-8577 , Japan
-
- Tatsuya Takahashi
- Graduate School of Life Sciences, Ritsumeikan University, Kusatsu, Shiga 525-8577 , Japan
-
- Yuichi Kitagawa
- Division of Materials Chemistry, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido 060-8628 , Japan
-
- Hitoshi Tamiaki
- Graduate School of Life Sciences, Ritsumeikan University, Kusatsu, Shiga 525-8577 , Japan
Search this article
Description
<jats:title>Abstract</jats:title> <jats:p>p-Aminopyridines were oxidatively substituted at the C31-position of methyl pyropheophorbide-a, a chlorophyll-a derivative. The electron-donating p-dimethylamino groups induced silver metallation during the substitution and inhibited the electron-transfer quenching of fluorescence emission in the metal-free C31-cationic pyridinio adducts prepared by the acidic demetallation of the initially isolated Ag-chlorins.</jats:p>
Journal
-
- Bulletin of the Chemical Society of Japan
-
Bulletin of the Chemical Society of Japan 94 (4), 1201-1203, 2021-02-03
Oxford University Press (OUP)
- Tweet
Details 詳細情報について
-
- CRID
- 1360006529434573952
-
- NII Article ID
- 130008037346
-
- ISSN
- 13480634
- 00092673
-
- Article Type
- journal article
-
- Data Source
-
- Crossref
- CiNii Articles
- KAKEN
- OpenAIRE