Chiral Peropyrene by Selective Dimerization of Phenalenyl

Two aryl substituted phenalenyl derivatives\nwere synthesized, providing\nan opportunity to study the steric effects on selectivity of phenalenyl\ndimerization. Owing to σ-dimerization serving as the decisive\nstep in phenalenyl–peropyrene transformation, a chiral peropyrene\ncompound was generated by dimerization of triarylphenalenyl, while\ntetraarylphenalenyl did not afford any dimerized product. The structure\nand properties of chiral peropyrene were elaborated. Our study showcases\nthat phenalenyl dimerization could function as a useful tool to synthesize\nfascinating π-conjugated hydrocarbons.

Publication Details

Journal
Figshare
Published
2024-10-15
DOI
https://doi.org/10.1021/acs.orglett.4c03235.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
Field-Weighted Citation Impact
0.00
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Chiral Peropyrene by Selective Dimerization of Phenalenyl

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Mycorrhizal Fungi and Plant Interactions
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Chiral Peropyrene by Selective Dimerization of Phenalenyl

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Abstract

Two aryl substituted phenalenyl derivatives\nwere synthesized, providing\nan opportunity to study the steric effects on selectivity of phenalenyl\ndimerization. Owing to σ-dimerization serving as the decisive\nstep in phenalenyl–peropyrene transformation, a chiral peropyrene\ncompound was generated by dimerization of triarylphenalenyl, while\ntetraarylphenalenyl did not afford any dimerized product. The structure\nand properties of chiral peropyrene were elaborated. Our study showcases\nthat phenalenyl dimerization could function as a useful tool to synthesize\nfascinating π-conjugated hydrocarbons.

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Mycorrhizal Fungi and Plant Interactions
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Chiral Peropyrene by Selective Dimerization of Phenalenyl · Figshare (2024) | TGRS Research Map | TGRS