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• W3132019411 endingPage "2221" @default.
• W3132019411 startingPage "2217" @default.
• W3132019411 abstract "Symmetric ladder-type oligo(p-aniline)s and poly(p-aniline)s were successfully synthesized by an intramolecular ring closure in a highly efficient SNAr reaction from oligo(p-phenylene)s and poly(p-phenylene)s with fluorine (F) and secondary amine (NH) groups. Unlike Cadogan ring closure, the newly designed cyclization reaction will not produce a mixture of symmetric and nonsymmetric structures. Moreover, the introduction of the F atom does not hinder Suzuki polymerization. The result indicates that preparing regular oligomers and polymers with a nitrogen bridge is possible." @default.
• W3132019411 created "2021-03-01" @default.
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• W3132019411 date "2021-02-26" @default.
• W3132019411 modified "2023-10-03" @default.
• W3132019411 title "Effective Synthesis of Ladder-type Oligo(<i>p</i>-aniline)s and Poly(<i>p</i>-aniline)s via Intramolecular S_NAr Reaction" @default.
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• W3132019411 doi "https://doi.org/10.1021/acs.orglett.1c00363" @default.
• W3132019411 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33635084" @default.
• W3132019411 hasPublicationYear "2021" @default.
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