Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5917
Title: Symmetric 32π (1.0.1.0.1.0.1) Core-Modified Heptaphyrins from Asymmetric Building Block
Authors: GUPTA, PRACHI
ANAND, V. G.
Dept. of Chemistry
Keywords: Chemistry
2021-JUN-WEEK1
TOC-JUN-2021
2021
Issue Date: May-2021
Publisher: American Chemical Society
Citation: Organic Letters, 23(9), 3481–3485.
Abstract: An asymmetrical precursor with three thiophene subunits on condensation with a thiophene/furan diol yield a symmetrical 32π heptaphyrin. Here are the first examples of pyrrole-free antiaromatic heptaphyrin synthesized by the acid assisted condensation reaction, followed by an oxidative α–α coupling between the terminal thiophene rings. The macrocycles attains a slightly bent configuration, which undergoes reversible two-electron oxidation between a neutral 4nπ and (4n + 2)π dication state.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5917
https://doi.org/10.1021/acs.orglett.1c00923
ISSN: 1523-7060
1523-7052
Appears in Collections:JOURNAL ARTICLES

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