The Primary Formation of a Cationic C10-Pyridinio-Chlorophyll-α Derivative by Chemical/Electrochemical Oxidation and the Physico-Chemical Properties of Regioisomeric meso-Adducts
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<jats:title>Abstract</jats:title> <jats:p>A cationic pyridinium group was introduced to a zinc chlorophyll-a derivative at the meso-positions via its (electro)chemically oxidized cationic radical state. The coupling reactions of zinc methyl mesopyropheophorbide-a with pyridine afforded 5-, 10-, and 20-pyridinio-chlorins that were successfully separated by reversed-phase HPLC. Their 1D/2D-NMR showed the major adduct to be the C10–N+C5H5 regioisomer. Substitution with the meso-pyridinio groups red-shifted their visible absorption bands in a solution.</jats:p>
収録刊行物
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- Bulletin of the Chemical Society of Japan
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Bulletin of the Chemical Society of Japan 91 (12), 1724-1730, 2018-12
Tokyo : Chemical Society of Japan
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詳細情報 詳細情報について
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- CRID
- 1520291855732850176
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- NII論文ID
- 130007531012
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- NII書誌ID
- AA00580132
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- ISSN
- 00092673
- 13480634
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- NDL書誌ID
- 029420509
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- 本文言語コード
- en
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- NDL 雑誌分類
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- ZP1(科学技術--化学・化学工業)
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- データソース種別
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- NDL
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