Solution-phase molecular recognition of an azafullerene-quinoline dyad by a face-to-face porphyrin-dimer tweezer
Author:
Affiliation:
1. Theoretical and Physical Chemistry Institute
2. National Hellenic Research Foundation
3. 11635 Athens
4. Greece
5. Department of Chemistry
6. University of Patras
7. University Campus
8. 26504 Rio-Patras
Abstract
Azafullerene C59N was modified by a pentafluoroquinoline (FQ) derivative, the amphoteric quinoline domain was utilized for the molecular recognition of C59N-FQ by a porphyrin-dimer (H2P)2 and host–guest interactions in (H2P)2/C59N-FQ were assessed.
Funder
European Regional Development Fund
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA06195F
Reference62 articles.
1. There Is a Hole in My Bucky
2. Isolation of the Heterofullerene C 59 N as Its Dimer (C 59 N) 2
3. Heterofullerenes
4. Azafullerene C59 N in Donor-Acceptor Dyads: Synthetic Approaches and Properties
5. C59N+: A key intermediate in azaheterofullerene chemistry
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1. Exploring the chemical physics in tetraphenylporphyrin-N-methylfulleropyrrolidine supramolecular complex by spectroscopic investigations and quantum chemical calculations;Chemical Physics;2024-06
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
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