William E. Acree, Jr. 1 2.2e+01 Ambient temperature 2 2.2 °C -3 2.1e-03 Amount concentration (1) 2 2.1 mol/dm³ 1 1 Solubility, Solubility data series Analytical balance and centrifuge. Excess solute and solvent allowed to equilibrate in a room temperature bath for 30 minutes. Solution centrifuged for about 5 minutes and filtered through a 0.45 µm HPLC syringe filtered. Three 1.0 mls were removed and placed in tared vials, which were then placed in a heated oil bath to facilitate solvent evaporation. Concentrations determined gravimetrically from the weight of the solid residue. The International Union of Pure and Applied Chemistry Scrivens, W. A.; Tour, J. M.; J. Chem. Soc.; Chem. Commun. 1993, 1207-1209. paper https://doi.org/10.1039/c39930001207 99685-96-8 1 C60 InChI=1S/C60/c1-2-5-6-3(1)8-12-10-4(1)9-11-7(2)17-21-13(5)23-24-14(6)22-18(8)28-20(12)30-26-16(10)15(9)25-29-19(11)27(17)37-41-31(21)33(23)43-44-34(24)32(22)42-38(28)48-40(30)46-36(26)35(25)45-39(29)47(37)55-49(41)51(43)57-52(44)50(42)56(48)59-54(46)53(45)58(55)60(57)59 XMWRBQBLMFGWIX-UHFFFAOYSA-N 720.642 Buckminsterfullerene Purity and chemical source were not given in the paper. 103-65-1 2 C9H12 InChI=1S/C9H12/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3 ODLMAHJVESYWTB-UHFFFAOYSA-N 120.192 Propylbenzene Purity and chemical source were not given in the paper. Buckminsterfullerene with n-Propylbenzene