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DALTON TRANSACTIONS
Volume -, Issue -, Pages -Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3dt02048g
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The redox reaction between a bulky BODIPY and a magnesium(i) reducing agent results in the formal one-electron reduction of the BODIPY, producing a dipyrromethene-centred radical compound that forms dimers via C-C bond formation. On the other hand, reduction with magnesium anthracene leads to the formal two-electron reduction of the BODIPY, leading to the formation of the corresponding anion.
The redox reaction between a bulky BODIPY and a magnesium(i) reducing agent leads to the formal one-electron reduction of the BODIPY, initially generating a dipyrromethene-centred radical compound that dimerises via C-C bond formation. In contrast, reduction with magnesium anthracene leads to the formal two-electron reduction of the BODIPY, resulting in the formation of the corresponding anion.
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