z-logo
Premium
Fluorinated fullerenes: Synthesis and characterization
Author(s) -
Selig H.,
Kniaz K.,
Vaughan G.B.M.,
Fischer J. E.,
Smith A. B.
Publication year - 1994
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.19940820111
Subject(s) - fullerene , stoichiometry , halogen , oxygen , hydrolysis , characterization (materials science) , hexagonal crystal system , chemistry , mass spectrometry , crystallography , analytical chemistry (journal) , materials science , organic chemistry , nanotechnology , chromatography , alkyl
The existence of the fully fluorinated fullerene, C 60 F 60 , is still subject to controversy. Mass spectrometric evidence shows that it exists, albeit in trace amounts five orders of magnitude in concentration below the most abundant C 60 F 40‐42 . Generally, mixtures of C 60 F n are obtained where n ranges from 30 to 52, depending on fluorinating conditions. The species with n = 36 is particularly stable. Attempts to increase n by use of the strongly fluorinating halogen fluorides, ClF 3 or BrF 5 , have led to products C 60 F X X y O z (X = Br or Cl), where the origin of the oxygen is probably hydrolysis during analysis. Fluorinated C 60 crystallizes as a mixture of hexagonal close packed (40%) and face‐centered cubic (60%) phases. X‐ray analysis yields an average C‐F bond length of 1.49A. Fluorination of C 70 leads to mixtures with maximum average stoichiometries of C 70 F 52 .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom