Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9439
Title: Reversible Ring Oxidation of 48π Planar Nonaphyrins to Open Shell 46π Dications
Authors: GOPALAKRISHNA, TULLIMILLI Y.
BASAVARAJAPPA, ASHOKKUMAR
UDAYA, HOSAHALLI S.
Furukawa, Ko
Wu, Jishan
ANAND, VENKATARAMANARAO G.
Dept. of Chemistry
Keywords: Diradicaloids
Macrocycles
Porphyrinoids
Aromaticity
Heterocycles
2025-MAR-WEEK4
TOC-MAR-2025
2025
Issue Date: Mar-2025
Publisher: Wiley
Citation: Chemistry- A European Journal
Abstract: Two properties of symmetric cube transfers of modular formsWe report the synthesis and characterization of 48π nonaphyrins, a novel class of planar expanded porphyrinoids exhibiting distinct electronic properties compared to their 32π congeners. Single-crystal X-ray diffraction studies revealed heterocycle dependent structural topology for these macrocycles. All the isolated nonaphyrins display weak paratropic ring current effects and undergo reversible two-electron ring oxidation to yield the respective 46π dicationic diradicaloid species. The formation of oxidized diradicaloid species was confirmed by ESR spectroscopy, spectro-electrochemical measurements and further supported by quantum chemical calculations.
URI: https://doi.org/10.1002/chem.202500555
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9439
ISSN: 1521-3765
0947-6539
Appears in Collections:JOURNAL ARTICLES

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