Isolation and characterisation of two oxahomofullerene derivatives of C60F18
Isolation and characterisation of two oxahomofullerene derivatives of C60F18
From the products of the reaction of [60]fullerene with K2PtF6 under vacuum at 465 degreesC we have isolated two minor isomers of C60F18O, and characterised them by EI mass spectrometry, IR and F-19 NMR spectroscopy. Calculations, the NMR spectra, thermal degradation, and the lack of evidence for the existence of precursors for the formation of epoxides indicate that, like the major isomer recently fully characterised, both are ethers. The results emphasise that oxides of fullerene derivatives may be either epoxides or ethers. Calculations show a correlation between length of the FC-CF bonds and heat of formation of the ethers, reinforcing our previous conclusion that the bond length is a driving force for ether formation. Given this, one can anticipate ether formation in other derivatised fullerenes which possess a long alpha,beta -bond.
2212-2216
Boltalina, O. V.
c91e33b3-7da7-4481-95f4-92fce2a56e46
De La Vaissiere, B.
64970e15-5362-467b-91d8-20d46bd8735f
Fowler, P. W.
ef41de08-2322-4b5f-ad11-fea288519277
Lukonin, A. Y.
758144bd-dfdd-42fa-bf14-c73bf69e8f53
Abdul-Sada, A. K.
3cb560e4-31f6-4ba9-a163-10676c653f3b
Street, J. M.
67b5e419-1784-425f-a913-f67d1fae8b22
Taylor, R.
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2000
Boltalina, O. V.
c91e33b3-7da7-4481-95f4-92fce2a56e46
De La Vaissiere, B.
64970e15-5362-467b-91d8-20d46bd8735f
Fowler, P. W.
ef41de08-2322-4b5f-ad11-fea288519277
Lukonin, A. Y.
758144bd-dfdd-42fa-bf14-c73bf69e8f53
Abdul-Sada, A. K.
3cb560e4-31f6-4ba9-a163-10676c653f3b
Street, J. M.
67b5e419-1784-425f-a913-f67d1fae8b22
Taylor, R.
1abcd415-ae2c-4e95-a761-6948ce7f4d32
Boltalina, O. V., De La Vaissiere, B., Fowler, P. W., Lukonin, A. Y., Abdul-Sada, A. K., Street, J. M. and Taylor, R.
(2000)
Isolation and characterisation of two oxahomofullerene derivatives of C60F18.
Journal of the Chemical Society, Perkin Transactions 2, (11), .
(doi:10.1039/b005504m).
Abstract
From the products of the reaction of [60]fullerene with K2PtF6 under vacuum at 465 degreesC we have isolated two minor isomers of C60F18O, and characterised them by EI mass spectrometry, IR and F-19 NMR spectroscopy. Calculations, the NMR spectra, thermal degradation, and the lack of evidence for the existence of precursors for the formation of epoxides indicate that, like the major isomer recently fully characterised, both are ethers. The results emphasise that oxides of fullerene derivatives may be either epoxides or ethers. Calculations show a correlation between length of the FC-CF bonds and heat of formation of the ethers, reinforcing our previous conclusion that the bond length is a driving force for ether formation. Given this, one can anticipate ether formation in other derivatised fullerenes which possess a long alpha,beta -bond.
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Published date: 2000
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Local EPrints ID: 18991
URI: http://eprints.soton.ac.uk/id/eprint/18991
ISSN: 1364-5471
PURE UUID: ffa42438-38a6-4b97-956f-78fb9fb957ad
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Date deposited: 21 Dec 2005
Last modified: 15 Mar 2024 06:09
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Author:
O. V. Boltalina
Author:
B. De La Vaissiere
Author:
P. W. Fowler
Author:
A. Y. Lukonin
Author:
A. K. Abdul-Sada
Author:
J. M. Street
Author:
R. Taylor
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