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Phenylene-bridged bis(benzimidazolium) (BBIm(2+)): a dicationic organic photoredox catalyst
A dicationic photoredox catalyst composed of phenylene-bridged bis(benzimidazolium) (BBIm(2+)) was designed, synthesised and demonstrated to promote the photochemical decarboxylative hydroxylation and dimerisation of carboxylic acids. The catalytic activity of BBIm(2+) was higher than that for a mon...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162872/ https://www.ncbi.nlm.nih.gov/pubmed/34094425 http://dx.doi.org/10.1039/d0sc03958f |
Sumario: | A dicationic photoredox catalyst composed of phenylene-bridged bis(benzimidazolium) (BBIm(2+)) was designed, synthesised and demonstrated to promote the photochemical decarboxylative hydroxylation and dimerisation of carboxylic acids. The catalytic activity of BBIm(2+) was higher than that for a monocation analogue, suggesting that the dicationic nature of BBIm(2+) plays a key role in these decarboxylative reactions. The rate constant for the decay of the triplet–triplet absorption of the excited BBIm(2+) increased with increasing concentration of the carboxylate anion with a saturated dependence, suggesting that photoinduced electron transfer occurs within the ion pair complex composed of the triplet excited state of BBIm(2+) and a carboxylate anion. |
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