2011
DOI: 10.1134/s1070363211080159
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Mechanochemical synthesis and properties of fullerene derivatives

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Cited by 4 publications
(9 citation statements)
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“…Meanwhile, only a small amount of alkali in comparison to the method reported before is required as a catalyst to avoid the use of excessive hydroxylation reagent. [ 39,41–43 ] Furthermore, synthetic conditions of fullerenols are optimized (Table S1, Supporting Information, Figure 1b–e, Figure S1–S5, Supporting Information) by exploring the influence of the amount of catalyst NaOH and hydroxylation reagent H 2 O 2 and lapping ways in the process of synthesis on the molecular structure and yield of as‐prepared fullerenol products with qualitative and quantitative characterization (details are listed at the additional discussion of supporting information). Finally, it was chosen as the optimized synthetic conditions that the C 60 to NaOH mass ratio of 10:1, the C 60 to H 2 O 2 molar ratio of 0.139:2, and mechanical ball milling at a speed of 300 rpm, to prepare moderate hydroxyl number fullerenols C 60 (OH) 20 with good water solubility.…”
Section: Resultsmentioning
confidence: 99%
“…Meanwhile, only a small amount of alkali in comparison to the method reported before is required as a catalyst to avoid the use of excessive hydroxylation reagent. [ 39,41–43 ] Furthermore, synthetic conditions of fullerenols are optimized (Table S1, Supporting Information, Figure 1b–e, Figure S1–S5, Supporting Information) by exploring the influence of the amount of catalyst NaOH and hydroxylation reagent H 2 O 2 and lapping ways in the process of synthesis on the molecular structure and yield of as‐prepared fullerenol products with qualitative and quantitative characterization (details are listed at the additional discussion of supporting information). Finally, it was chosen as the optimized synthetic conditions that the C 60 to NaOH mass ratio of 10:1, the C 60 to H 2 O 2 molar ratio of 0.139:2, and mechanical ball milling at a speed of 300 rpm, to prepare moderate hydroxyl number fullerenols C 60 (OH) 20 with good water solubility.…”
Section: Resultsmentioning
confidence: 99%
“…34,36 Nevertheless, when conducting the reaction in air a totally different product was obtained. 96,97 Forty-five milligrams of C 60 with about 250 equiv. of KOH were mixed in a Wig-L-Bug mill in air for 1 h, and then quenched with water, C 60 (OH) n (n = 27.2) was acquired in 84% yield.…”
Section: Oxygenation Of C 60mentioning
confidence: 99%
“…The same reaction in a planetary ball mill for 1 h at 550 rpm afforded fullerenols with an empirical formula of C 60 (OH) 27.6 H 7.1 . 97 Replacing KOH with LiNH 2 led to the adduct containing both OH and NH 2 groups (Scheme 45). 97 The empirical formula calculated from the results of elemental analysis is C 60 (OH) 8.7 -(NH 2 ) 3.5 H 3.5 Á3HCl.…”
Section: Oxygenation Of C 60mentioning
confidence: 99%
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“…Adduct FOL synthesised in two variants was chosen as the water-soluble nanocarbon compound: FOL-1the product of the mechanochemical hydroxylation of a C 60 /C 70 mixture; FOL-2 -polyhydroxylated fullerene of composition C 60 (OH) 28 [13]. For the manufacture of specimens, one layer of finished reinforcing glass fabric was placed between two layers of the untreated film (the film technology method [14]) with heating to 220-235°C in a melt under a pressure of 2.5 MPa.…”
Section: Methodsmentioning
confidence: 99%