Nucleophilic substitution of fluorinated C60

Roger Taylor; John H. Holloway; Eric G. Hope; Anthony G. Avent; G. John Langley; T. John Dennis; Jonathan P. Hare; Harold W. Kroto; David R.M. Walton

doi:10.1039/C39920000665

Nucleophilic substitution of fluorinated C₆₀

Roger Taylor^*, John H. Holloway, Eric G. Hope, Anthony G. Avent, G. John Langley, T. John Dennis, Jonathan P. Hare, Harold W. Kroto, David R.M. Walton

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

83 Citations (Scopus)

Abstract

Highly fluorinated C₆₀ is extremely reactive towards nucleophilic substitution, which may proceed by a novel mechanism; attachment of a wide range of functional groups to the fullerene cage can thus be accomplished.

Original language	English
Pages (from-to)	665-667
Number of pages	3
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	9
DOIs	https://doi.org/10.1039/C39920000665
Publication status	Published - 1992
Externally published	Yes

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@article{09deadeb8a9f48a98faa74555a29672a,

title = "Nucleophilic substitution of fluorinated C60",

abstract = "Highly fluorinated C60 is extremely reactive towards nucleophilic substitution, which may proceed by a novel mechanism; attachment of a wide range of functional groups to the fullerene cage can thus be accomplished.",

author = "Roger Taylor and Holloway, {John H.} and Hope, {Eric G.} and Avent, {Anthony G.} and Langley, {G. John} and Dennis, {T. John} and Hare, {Jonathan P.} and Kroto, {Harold W.} and Walton, {David R.M.}",

year = "1992",

doi = "10.1039/C39920000665",

language = "English",

pages = "665--667",

journal = "Journal of the Chemical Society, Chemical Communications",

issn = "0022-4936",

number = "9",

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T1 - Nucleophilic substitution of fluorinated C60

AU - Taylor, Roger

AU - Holloway, John H.

AU - Hope, Eric G.

AU - Avent, Anthony G.

AU - Langley, G. John

AU - Dennis, T. John

AU - Hare, Jonathan P.

AU - Kroto, Harold W.

AU - Walton, David R.M.

PY - 1992

Y1 - 1992

N2 - Highly fluorinated C60 is extremely reactive towards nucleophilic substitution, which may proceed by a novel mechanism; attachment of a wide range of functional groups to the fullerene cage can thus be accomplished.

AB - Highly fluorinated C60 is extremely reactive towards nucleophilic substitution, which may proceed by a novel mechanism; attachment of a wide range of functional groups to the fullerene cage can thus be accomplished.

UR - http://www.scopus.com/inward/record.url?scp=37049072551&partnerID=8YFLogxK

U2 - 10.1039/C39920000665

DO - 10.1039/C39920000665

M3 - Article

AN - SCOPUS:37049072551

SN - 0022-4936

SP - 665

EP - 667

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 9

ER -

Nucleophilic substitution of fluorinated C₆₀

Abstract

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