Structural analysis of products from the C60-piperazine reaction. Consistent geometric distortions of the fullerene core upon adduct formation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Fullerenes Synthesis, Properties and Chemistry of Large Carbon Clusters;Hirsch,1992
2. Globe-trotting Hydrogens on the Surface of the Fullerene Compound C60H6(N(CH2CH2)2O)6
3. The absence of ‘globe-trotting’ hydrogen on the surfaces of aminated fullerenes: 3-D hydrogen bonding between aminated fullerenes and water revealed
4. Diamino and Tetraamino Derivatives of Buckminsterfullerene C60
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1. A sonochemical synthesis of the piperazine-containing adducts of the C60 fullerene;Fullerenes, Nanotubes and Carbon Nanostructures;2021-01-18
2. Fullerenes and their applications;Handbook of Carbon-Based Nanomaterials;2021
3. The directional character of the piperazine double addition product, e{N(CH2CH2)2N}2C60, as a building block for forming crystalline fullerene polymers;CrystEngComm;2018
4. Piperazine-functionalized C60 and diiodine or iodine monochloride as components in forming supramolecular assemblies;Dalton Transactions;2017
5. Piperazine Functionalization of C70for Incorporation into Supramolecular Assemblies;Chemistry - A European Journal;2016-11-17
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