A wide-range of redox states of core-modified expanded porphyrinoids

Core-modified hexaphyrin and octaphyrin display four- and six-electron reversible redox reactions respectively, to alternate between aromatic and anti-aromatic states of a given macrocycle. We have identified and isolated a hexaphyrin in three discrete states with 26π, 28π and 30π electrons that are...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2019-06, Vol.55 (47), p.6763-6766
Hauptverfasser: Ambhore, Madan D, Basavarajappa, Ashokkumar, Anand, Venkataramanarao G
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Sprache:eng
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Zusammenfassung:Core-modified hexaphyrin and octaphyrin display four- and six-electron reversible redox reactions respectively, to alternate between aromatic and anti-aromatic states of a given macrocycle. We have identified and isolated a hexaphyrin in three discrete states with 26π, 28π and 30π electrons that are inter-convertible with each other. Its higher congener, octaphyrin, can exist as four discrete species with 34, 36, 38 and 40 electrons. A difference of two-electrons between each stable redox state is reflected by the significant variation in their electronic and structural properties as characterized in both solution and solid states. The observed redox inter-conversions were achieved by a combination of both proton coupled electron-transfer (PCET) and electron-transfer (ET) processes respectively. Core-modified hexaphyrin and octaphyrin display four- and six-electron reversible redox reactions respectively, to alternate between aromatic and anti-aromatic states of a given macrocycle.
ISSN:1359-7345
1364-548X
DOI:10.1039/c9cc02326g