Hydro-aza-(C59N)fullerenes: Formation Mechanism and Hydrogen Substitution-Reference-Cited by-同舟云学术

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Hydro-aza-(C59N)fullerenes: Formation Mechanism and Hydrogen Substitution

Published:2016-07-19 Issue:38 Volume:22 Page:13575-13581
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Eigler Regina¹,Heinemann Frank W.²,Hirsch Andreas¹^ORCID

Affiliation:

1. Department Chemie und Pharmazie; Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU); Henkestrasse 42 91054 Erlangen Germany

2. Department Chemie und Pharmazie; Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU); Egerlandstrasse 1 91058 Erlangen Germany

Funder

Graduate School of Molecular Science of the Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201505115/fullpdf

Reference33 articles.

1. Heterofullerenes

2. Isolation of the Heterofullerene C 59 N as Its Dimer (C 59 N) 2

3. A new route to nitrogen heterofullerenes and the first synthesis of (C69N)2

4. Preparation of Azafullerene Derivatives from Fullerene-Mixed Peroxides and Single Crystal X-ray Structures of Azafulleroid and Azafullerene

5. Synthesis of hydroazafullerene C59HN, the parent hydroheterofullerene

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1. Effects of B and N doping/codoping on the adsorption behavior of C60 fullerene towards aspirin: A DFT investigation;Journal of Molecular Liquids;2021-11

2. 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

3. A first-principles evaluation on the interaction of 1,3,4-oxadiazole with pristine and B-, Al-, Ga-doped C60 fullerenes;Journal of Molecular Liquids;2021-08

4. Hetero-fullerenes C59M (M = B, Al, Ga, Ge, N, P, As) for sulfur dioxide gas sensing: Computational approach;Chemical Physics;2020-02

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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