Sulfolenocorrole as a Chameleon-Like Tecton Enabling the Construction of Multiring Fused Corroles

Abstract In addition to β,β-fusions based on the Diels–Alder reaction of sulfolenocorrole, meso,β-fusion has been realized, enabling the synthesis of multiring fused corroles (CuF3x). The obtained unique conjugation systems afford intense π-stacking and pronounced bathochromic absorption with a broad peak around 1280 nm. Upon theoretical calculations and NMR analysis, the multifusions suppress the noninnocent feature of the corrole ligand; meanwhile, CuF3x and HF3M are proposed to be weakly antiaromatic and nonaromatic, respectively.

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Publication Details

Journal
Organic Letters
Published
2026-10-03
DOI
https://doi.org/10.1021/acs.orglett.6c03748
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
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article

Sulfolenocorrole as a Chameleon-Like Tecton Enabling the Construction of Multiring Fused Corroles

Chengjie Li, Qinlei Liu, Danni Gong, Zhaowen Ye et al.
Organic Letters
Porphyrin and Phthalocyanine Chemistry
article

Sulfolenocorrole as a Chameleon-Like Tecton Enabling the Construction of Multiring Fused Corroles

Chengjie Li, Qinlei Liu, Danni Gong, Zhaowen Ye, Mengyi Hu, Junyang Wang, Qiushuang Li
article en

Abstract

Abstract In addition to β,β-fusions based on the Diels–Alder reaction of sulfolenocorrole, meso,β-fusion has been realized, enabling the synthesis of multiring fused corroles (CuF3x). The obtained unique conjugation systems afford intense π-stacking and pronounced bathochromic absorption with a broad peak around 1280 nm. Upon theoretical calculations and NMR analysis, the multifusions suppress the noninnocent feature of the corrole ligand; meanwhile, CuF3x and HF3M are proposed to be weakly antiaromatic and nonaromatic, respectively.

Organic Letters
East China University of Science and Technology (CN)
Openalex Percentile: Top 26%
Porphyrin and Phthalocyanine Chemistry
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