1999
DOI: 10.1006/jcht.1999.0544
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The standard molar enthalpy of formation of fluorofullereneC60F48

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Cited by 39 publications
(20 citation statements)
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“…This hypothesis is supported by our observations of the partial or even complete defluorination of fullerene fluorides upon the increase of the donor concentration. The lower strength of C F bonds in fluorofullerenes relative to sterically unstrained organic compounds (the average C F bond energy in C 60 F 2n does not exceed 300 kJ/mol and decreases from C 60 F 36 to C 60 F 48 ) [28,29] and higher stability of the closed-shell anionic species can serve as additional driving forces for the processes of F atom loss and charging. On one hand, such defluorination processes that accompany ESI MS of fluorofullerenes can be regarded as a drawback of the ESI-based method of anion production as compared to the gas-phase electron-capture techniques, since it is more difficult to generate molecular ions or doubly charged anions of the parent molecules.…”
Section: Experimental and Theoretical Methodsmentioning
confidence: 99%
“…This hypothesis is supported by our observations of the partial or even complete defluorination of fullerene fluorides upon the increase of the donor concentration. The lower strength of C F bonds in fluorofullerenes relative to sterically unstrained organic compounds (the average C F bond energy in C 60 F 2n does not exceed 300 kJ/mol and decreases from C 60 F 36 to C 60 F 48 ) [28,29] and higher stability of the closed-shell anionic species can serve as additional driving forces for the processes of F atom loss and charging. On one hand, such defluorination processes that accompany ESI MS of fluorofullerenes can be regarded as a drawback of the ESI-based method of anion production as compared to the gas-phase electron-capture techniques, since it is more difficult to generate molecular ions or doubly charged anions of the parent molecules.…”
Section: Experimental and Theoretical Methodsmentioning
confidence: 99%
“…The energy of combustion of C 60 F 48 for burning in a rotating bomb calorimeter (724 638AE163 kJ mol 71 ) and the standard molar enthalpy of formation of C 60 F 48 in the crystalline state have been determined 64 (see Table 7).…”
Section: Chemical Properties Of Fluorofullerenesmentioning
confidence: 99%
“…It is of interest to compare these results with the data on the thermodynamic stability of highly fluorinated fullerenes. The measurements of the combustion energies for C 60 , 46 C 60 F 36 47 and C 60 F 48 48 and the enthalpies of sublimation of these compounds gave average values for the C7F bond energy in C 60 F 36 and C 60 F 48 fluorofullerenes equal to 295.0 AE 5.6 and 287.5 AE 3.5 kJ mol 71 , respectively. These data also made it possible to estimate the enthalpy of the reaction C 60 F 36 + 12 F = C 60 F 48 per fluorine atom; the result was 265 kJ mol 71 .…”
Section: B Fluorofullerenesmentioning
confidence: 99%
“…The average C7F bond energies in the C 60 F 48 (g) and C 60 F 36 (g) molecules are 287.5 and 295 kJ mol 71 , respectively. 47,48 This allows one to calculate the average C7F bond energy for the addition of 12 fluorine atoms to the C 60 F 36 molecule, which equals 265 kJ mol 71 (see Section VI.3.b). On the basis of these data, the jump in the C7F bond energy on passing from n < 36 to n > 36 in the series of C 60 F n is estimated as 30 kJ mol 71 .…”
Section: Selectivity Of Fluorinationmentioning
confidence: 99%
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