Literature DB >> 34124860

Synthesis of 8,12-Dibromocorrole and Its Transformation to Antiaromatic 8,10-Fused Iminoisocorrole with a Polarized Resonance Contribution.

Kento Ueta1, Akito Nakai1, Takayuki Tanaka2, Atsuhiro Osuka3.   

Abstract

8,12-Dibromo-5,15-bis(pentafluorophenyl)corrole and its Ag(III) complex were prepared via intramolecular oxidative coupling of a 8,12-dibromobilane precursor. The Ag(III) complex was allowed for further transformation via Suzuki coupling reaction. Thus, 2-aminophenyl group was coupled at one of the β -positions, and subsequent demetalation followed by oxidation with MnO 2 afforded 8,10-fused iminoisocorrole in good yields. The iminoisocorrole exhibited weak antiaromaticity due to the C(+)-N(-) polarized resonance contribution as evidenced by 1 H NMR spectrum, UV/vis absorption spectra, cyclic voltammetry, and theoretical calculations.
© 2021 Wiley-VCH GmbH.

Entities:  

Keywords:  Suzuki coupling; antiaromaticity; corrole; cyclic voltammetry; isocorrole

Year:  2021        PMID: 34124860     DOI: 10.1002/asia.202100577

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  1 in total

1.  The Selective Monobromination of a Highly Sterically Encumbered Corrole: Structural and Spectroscopic Properties of Fe(Cl)(2-Bromo-5,10,15-tris(triphenyl)phenyl corrole).

Authors:  Jessica G Alvarado; Daniel C Cummins; Andrada Diaconescu; Maxime A Siegler; David P Goldberg
Journal:  J Porphyr Phthalocyanines       Date:  2021       Impact factor: 1.914

  1 in total

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