Switching the photo-induced energy and electron-transfer processes in BODIPY–phthalocyanine conjugates
Literature Information
Jian-Yong Liu, Eugeny A. Ermilov, Beate Röder, Dennis K. P. Ng
Two novel silicon(IV) phthalocyanines substituted axially with two BODIPY or mono-styryl BODIPY moieties have been synthesised, which exhibit predominantly a photo-induced energy or electron-transfer process in toluene depending on the axial substituents.
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![4,10-Dihydroxy-3H-pyrano[3,4,5-kl]xanthen-3-one structure 4,10-Dihydroxy-3H-pyrano[3,4,5-kl]xanthen-3-one structure](https://static.chemtradehub.com/structs/125/1259330-61-4-de48.webp)
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![[3-Fluoro-4-(1-pyrrolidinylcarbonyl)phenyl]boronic acid structure [3-Fluoro-4-(1-pyrrolidinylcarbonyl)phenyl]boronic acid structure](https://static.chemtradehub.com/structs/874/874289-09-5-e3d4.webp)
![4-Fluoro-2-(4-{[(3S,4R)-4-(2-hydroxy-2-propanyl)-3-pyrrolidinyl]amino}-6,7-dimethoxy-2-quinazolinyl)phenol hydrochloride (1:1) structure 4-Fluoro-2-(4-{[(3S,4R)-4-(2-hydroxy-2-propanyl)-3-pyrrolidinyl]amino}-6,7-dimethoxy-2-quinazolinyl)phenol hydrochloride (1:1) structure](https://static.chemtradehub.com/structs/143/1431697-96-9-619c.webp)