File(s) not publicly available
Isolation and characterisation of both the first fluoroxyfluorofullerene C60F17OF and oxahomofluorofullerenol C60F17O.OH
journal contribution
posted on 2023-06-08, 08:54 authored by Adam D Darwish, Ala'a K Abdul-Sada, Anthony G Avent, Joan M Street, Roger TaylorThe first fluoroxyfluorofullerene C60F17OF (A) has been isolated from the fluorination of [60]fullerene with a mixture of MnF3 and K2NiF6 at 480degreesC. This compound has a shorter HPLC retention time than the isomeric fluorofullerene ethers (oxahomofullerenes) and is less stable towards El mass spectrometry. It fragments by losing OF as a single entity and shows no formation Of C60O as a fragment ion. By contrast, the ethers fragment by first losing a number of F atoms and then CO, and ultimately show also the presence Of C60O, whilst epoxides lose CO as a main fragmentation step and do not give C60O. The first oxahomofluorofullerenol C60F17O.OH (B) has been isolated from the UV-irradiation of a toluene solution of C60F18 in air during 65 It and readily eliminates HF due to adjacent F and OH groups during El mass spectrometry. The structures of both the compounds have been deduced from I D and 2D F-19 NMR spectroscopy. Just as oxygen inserts into FC-CF bonds of C60F18 to give ethers, so insertion into a C-F bond gives A. The oxahomofluorofullerenol B is produced by S(N)2' substitution of F by OH, followed by oxygen insertion into a 6:5-bond (alphabeta to the OH group) giving a motif not seen previously in fluorofullerenes.
History
Publication status
- Published
Journal
Journal of Fluorine ChemistryISSN
0022-1139Publisher
ElsevierExternal DOI
Issue
2Volume
121Page range
185-192Department affiliated with
- Chemistry Publications
Full text available
- No
Peer reviewed?
- Yes
Legacy Posted Date
2012-02-06Usage metrics
Categories
No categories selectedKeywords
Licence
Exports
RefWorks
BibTeX
Ref. manager
Endnote
DataCite
NLM
DC