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85030192402
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Fullerenes were only obtained, when freshly destilled cyclopentadiene was used. Starting with the dimer pyrolysis took place before the retro-Diels-Alder reaction.
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For the symmetrically substituted methanofullerene 4 only four isomers are possible instead of six, because the isomers 4b and 4c respectively 4e and 4f are the same.
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f,r is calculated as the difference of the corresponding isomer and the stablest isomer.
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Li, Q.2
Khemani, K.C.3
Wudl, F.4
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75
-
-
0001686651
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b) Smith III, A. B.; Strongin, R. M.; Brard, L.; Furst, G. T.; Romanow, W. J.; Owens, K. G.; King, R. C. J. Am. Chem. Soc. 1993, 115, 5829-5830.
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(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 5829-5830
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-
Smith A.B. III1
Strongin, R.M.2
Brard, L.3
Furst, G.T.4
Romanow, W.J.5
Owens, K.G.6
King, R.C.7
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76
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85030188584
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-
note
-
It is not possible to use larger amounts, since a silica tube with this diameter would be blocked then.
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-
-
-
77
-
-
85030187763
-
-
note
-
Kroto and Taylor et al. first removed the acetone-soluble hydrocarbons, as fullerenes are nearly insoluble in acetone. But during our investigations we realised that in such low concentrations parts of the fullerenes are soluble in acetone: therefore we did not remove the acetone-soluble part.
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