Synthesis and Magnetic Property of 4,4′‐(2,6‐Anthracenediyl)bis(2,6‐di‐<i>tert</i>‐butylphenoxyl) Diradicaloids

Abstract Anthracene based phenoxyl diradicaloids are synthesized. The UV–vis spectra of them give absorption maxima around 700 nm attributes to the extended quinone structure. The diradical characters y of them are estimated as ∼0.6 from their static magnetic susceptibility and absorption maxima. The extended π‐conjugated anthracene‐linker enhances the diradical characters compared to the phenylene linker. It is noteworthy that these enhanced diradical characters are accomplished without steric effects.

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Publication Details

Journal
Macromolecular Chemistry and Physics
Published
2024-09-23
DOI
https://doi.org/10.1002/macp.202400195
Citations
1
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.25
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article

Synthesis and Magnetic Property of 4,4′‐(2,6‐Anthracenediyl)bis(2,6‐di‐tert‐butylphenoxyl) Diradicaloids

Toshiki Aoki, Masahiro Teraguchi, Takashi Kaneko, Ayako Ogawa
1 citations
Macromolecular Chemistry and Physics
Synthesis and Properties of Aromatic Compounds
0.25
article

Synthesis and Magnetic Property of 4,4′‐(2,6‐Anthracenediyl)bis(2,6‐di‐tert‐butylphenoxyl) Diradicaloids

Toshiki Aoki, Masahiro Teraguchi, Takashi Kaneko, Ayako Ogawa
article en
1 citations

Abstract

Abstract Anthracene based phenoxyl diradicaloids are synthesized. The UV–vis spectra of them give absorption maxima around 700 nm attributes to the extended quinone structure. The diradical characters y of them are estimated as ∼0.6 from their static magnetic susceptibility and absorption maxima. The extended π‐conjugated anthracene‐linker enhances the diradical characters compared to the phenylene linker. It is noteworthy that these enhanced diradical characters are accomplished without steric effects.

Macromolecular Chemistry and PhysicsVol. 226(4)
Niigata University (JP)
Openalex Percentile: Top 48%
Synthesis and Properties of Aromatic Compounds
0.25
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