Tether‐Directed Regioselective Synthesis of an Equatorial face Bisadduct of Azafullerene Using Cyclo ‐[2]‐octylmalonate
Author:
Affiliation:
1. Theoretical and Physical Chemistry InstituteNational Hellenic Research Foundation 48 Vassileos Constantinou Avenue 11635 Athens Greece
2. Department of ChemistryUniversity of Cyprus University str. 1, Building No. 13 2109 Aglantzia Nicosia Cyprus
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201900273
Reference43 articles.
1. Azafullerene C59 N in Donor-Acceptor Dyads: Synthetic Approaches and Properties
2. There Is a Hole in My Bucky
3. Isolation of the Heterofullerene C 59 N as Its Dimer (C 59 N) 2
4. C59N+: A key intermediate in azaheterofullerene chemistry
5. Axially Substituted Silicon Phthalocyanine as Electron Donor in a Dyad and Triad with Azafullerene as Electron Acceptor for Photoinduced Charge Separation
Cited by 3 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. 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. Solution-phase molecular recognition of an azafullerene-quinoline dyad by a face-to-face porphyrin-dimer tweezer;RSC Advances;2020
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