1994
DOI: 10.1038/368229a0
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Purification of C60 and C70 by selective complexation with calixarenes

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Cited by 612 publications
(442 citation statements)
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“…Thus, for 1:12 cage:fullerene extract molar ratios, mass spectra affords C 60 C4/C 70 C 4 and C 70 C4/C 84 C 4 ratios of 0. 18 Supplementary Fig. 12).…”
Section: Article Nature Communications | Doi: 101038/ncomms6557mentioning
confidence: 99%
See 1 more Smart Citation
“…Thus, for 1:12 cage:fullerene extract molar ratios, mass spectra affords C 60 C4/C 70 C 4 and C 70 C4/C 84 C 4 ratios of 0. 18 Supplementary Fig. 12).…”
Section: Article Nature Communications | Doi: 101038/ncomms6557mentioning
confidence: 99%
“…Host platforms containing extended p-systems have been designed because of their affinity towards the sphere-like unsaturated structure of fullerenes. In this line, several covalent or supramolecular approaches pursued include: (a) macrocyclic arene-based receptors [18][19][20][21][22][23][24] , (b) macrocyclic structures containing aromatic heterocycles [25][26][27][28] , (c) p-extended TTF receptors [29][30][31][32][33] and (d) macrocyclic or jawlike structures containing porphyrin moieties 17,[34][35][36][37][38][39][40][41][42][43][44][45] . Interestingly, Fujita and co-workers reported the use of the empty channels of a metal-organic framework (MOF) for encapsulating fullerenes upon soaking MOF crystals in fullerene-containing toluene.…”
mentioning
confidence: 99%
“…Fullerenes are typically synthesized as a mixture of sizes, however, owing to their solubility in common organic solvents 115 (e.g., toluene, CS 2 , ortho-dichlorobenzene), the separation of pure C 60 can be performed simply on the lab scale through chelation, 125 chromatography, or sublimation, and high yield industrial scale purifications are wellestablished. 126,127 Despite considerable progress toward product control and batch repeatability, there is still significant variation in the structures, morphologies, and properties of the other carbon nanomaterials between synthesis routes (and thus nanocarbon suppliers).…”
Section: Starting Materialsmentioning
confidence: 99%
“…To make a water-soluble fullerene was one of the great challenges in fullerene chemistry and scientific interest in the potential applications of these fascinating molecules [3] in the biochemical, biophysical and biological field. There were some introductions to make fullerene derivatives that were soluble in aqueous condition [4][5][6][7][8][9][10][11][12]. While a number of fullerene derivatives have been prepared for such a purpose, most of them have been of only poor aqueous solubility, the results of that have limited application in chemical reactions.…”
Section: Introductionmentioning
confidence: 99%