Literature DB >> 33645878

Rules of Nucleophilic Additions to Zigzag Nanographene Diones*.

Peter Ribar1, Leoš Valenta2, Tomáš Šolomek1,3,4, Michal Juríček2,3.   

Abstract

Nucleophilic addition of carbon-centered nucleophiles to nanographene ketones represents a valuable late-stage method for the functionalization of zigzag nanographenes, but its use is rare in the chemical literature. Using two model systems, non-Kekulé triangulene-4,8-dione and Kekulé anthanthrone, we identify unexpected regioselectivities and uncover the rules that govern these reactions. Considering the large number of nanographene ketones that have been reported since the pioneering work of Eric Clar, this method enables synthesis and exploration of hitherto unknown functionalized nanographenes.
© 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.

Entities:  

Keywords:  Fukui function analysis; Michael addition; nucleophilic addition; regioselectivity; zigzag nanographene

Year:  2021        PMID: 33645878     DOI: 10.1002/anie.202016437

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon.

Authors:  Leoš Valenta; Maximilian Mayländer; Pia Kappeler; Olivier Blacque; Tomáš Šolomek; Sabine Richert; Michal Juríček
Journal:  Chem Commun (Camb)       Date:  2022-03-01       Impact factor: 6.222

2.  Subphthalocyanine-triangulene dyads: Property tuning for light-harvesting device applications.

Authors:  Mads Georg Rasmussen; Malte Frydenlund Jespersen; Olivier Blacque; Kurt V Mikkelsen; Michal Juríček; Mogens Brøndsted Nielsen
Journal:  Energy Sci Eng       Date:  2022-01-17       Impact factor: 4.035

  2 in total

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