Literature DB >> 33544098

BNB-doped phenalenyls - aromaticity switch upon one-electron reduction.

Merian Crumbach1, Ozan Ayhan1, Lars Fritze1, Jan A P Sprenger1, Ludwig Zapf1, Maik Finze1, Holger Helten1.   

Abstract

Fully aromatic, luminescent, and highly robust BNB-doped phenalenyls have been prepared, which are isoelectronic to the phenalenyl cation. B-Fluoromesityl-substitution leads to fluorescence in an extremely narrow range and significant increase in the reduction potential. Detailed theoretical investigations revealed an intramolecular aromaticity switch upon one-electron reduction.

Entities:  

Year:  2021        PMID: 33544098     DOI: 10.1039/d0cc07671f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Reactions of a Four-Membered Borete with Carbon, Silicon, and Gallium Donor Ligands: Fused and Spiro-Type Boracycles.

Authors:  Zeynep Güven; Lars Denker; Hadi Dolati; Daniela Wullschläger; Bartosz Trzaskowski; René Frank
Journal:  Chemistry       Date:  2022-04-21       Impact factor: 5.020

  1 in total

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