Fullereen: erinevus redaktsioonide vahel

<ref name="test5">[http://www.bristol.ac.uk/Depts/Chemistry/MOTM/buckyball/c60a.htm Buckminsterfullerene: Molecule of the Month], Locke, W. (13 October 1996)</ref>

<ref name="test4">[http://en.wikipedia.org/wiki/Analytical_and_Bioanalytical_Chemistry Analytical and Bioanalytical Chemistry], 385: 6–7, Meija, J. (2006).</ref>

<ref name="Roubelakis">{{cite journal|doi=10.1021/jo070796l|year=2007|month=Aug|author=Roubelakis, Mm; Vougioukalakis, Gc; Orfanopoulos, M|title=Open-cage fullerene derivatives having 11-, 12-, and 13-membered-ring orifices: chemical transformations of the organic addends on the rim of the orifice|volume=72|issue=17|pages=6526–33|issn=0022-3263|pmid=17655360|journal=The Journal of organic chemistry}}</ref>

<ref name="test9">[http://en.wikipedia.org/wiki/Journal_of_Chemical_Physics Journal of Chemical Physics], Guo, T.; Smalley, R.E.; Scuseria, G.E. (1993). "Ab initio theoretical predictions of C28, C28H4, C28F4, (Ti at C28)H4, and M at C28 (M = Mg, Al, Si, S, Ca, Sc, Ti, Ge, Zr, and Sn)".</ref>

<ref name="test10">[http://www.tandfonline.com/doi/abs/10.1080/10641229608001534 "Early effects of C60Administration in Swiss Mice: A Preliminary Account forIn VivoC60Toxicity"], Moussa, F.; et al. (1996); Technology 4: 21.</ref>

<ref name="test11">Moussa, F.; et al. (1997). Proceedings of the Electrochemical Society 5: 332.</ref>