Literature DB >> 26607849

Azafullerene C59 in Donor-Acceptor Dyads: Synthetic Approaches and Properties.

Georgios Rotas1, Nikos Tagmatarchis2.   

Abstract

Energy conversion schemes have attracted considerable attention in recent years. A large amount of research effort has focused on fullerenes, particularly C60 and its derivatives, as suitable electron acceptors, owing to their outstanding properties. In this context, C59 N-based donor-acceptor systems have lately attracted attention, owing to their exceptional energy-and electron-transfer properties. As a result, chemical derivatization of C59 N plays an important role in the realization of the aforementioned systems. The current Minireview aims to familiarize researchers with the main aspects of azafullerene synthesis, chemistry, and photophysical properties, while it mainly focuses on the synthetic methodologies employed for as well as on energy conversion schemes of azafullerene-based donor-acceptor systems.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  azafullerene; charge transfer; donor-acceptor systems; functionalization; solar cells

Year:  2015        PMID: 26607849     DOI: 10.1002/chem.201502190

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

Review 1.  A Long-Lived Azafullerenyl Radical Stabilized by Supramolecular Shielding with a [10]Cycloparaphenylene.

Authors:  Anastasios Stergiou; Jérémy Rio; Jan H Griwatz; Denis Arčon; Hermann A Wegner; Christopher P Ewels; Nikos Tagmatarchis
Journal:  Angew Chem Int Ed Engl       Date:  2019-10-22       Impact factor: 15.336

2.  Solution-phase molecular recognition of an azafullerene-quinoline dyad by a face-to-face porphyrin-dimer tweezer.

Authors:  Anastasios Stergiou; Aikaterini K Andreopoulou; Joannis K Kallitsis; Nikos Tagmatarchis
Journal:  RSC Adv       Date:  2020-08-27       Impact factor: 4.036

  2 in total

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