Azafullerene C59 N in Donor-Acceptor Dyads: Synthetic Approaches and Properties-Reference-Cited by-同舟云学术

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

Published:2015-11-26 Issue:4 Volume:22 Page:1206-1214
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Rotas Georgios¹,Tagmatarchis Nikos¹

Affiliation:

1. Theoretical and Physical Chemistry Institute; National Hellenic Research Foundation; 48 Vassileos Contantinou Avenue Athens 11635 Greece

Funder

Greek General Secretariat for Research and Technology

European Commission

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference43 articles.

1. Tuning spectral properties of fullerenes by substitutional doping

2. Heterofullerenes

3. Synthesis, properties and chemistry of Aza[60]fullerene

4. Nitrogen Heterofullerenes

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Tether-directed regioselective synthesis of new cis-2ʹ azafullerene bisadducts;Carbon;2024-09

2. Pentagon-Fused Sumanenes on the Aromatic Peripheries en Route to the Bottom-Up Synthesis of Fullerenes;Synlett;2022-12-02

3. First Synthesis of the Inherently Chiral Trans ‐4′ Bisadduct of C 59 N Azafullerene by Using Cyclo‐ [2]‐dodecylmalonate as a Tether;Chemistry – A European Journal;2021-08-31

4. Aminated C20 fullerene as a promising nanosensor for detection of A-234 nerve agent;Computational and Theoretical Chemistry;2020-09

5. Solution-phase molecular recognition of an azafullerene-quinoline dyad by a face-to-face porphyrin-dimer tweezer;RSC Advances;2020

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