2004
DOI: 10.1016/j.tetlet.2004.09.072
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Hydrophilic [60]fullerene carboxylic acid derivatives retaining the original 60π electronic system

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Cited by 21 publications
(7 citation statements)
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“…The absorption spectrum shows a strong peak at 272 nm and broad bands at 300–400 nm, indicating the results from carboxylation of C 60 -TEG which has weak broad band at 260 nm and 350 nm [14]. These features are similar to those of the spectra of the hydrophilic fullerene carboxylic acid derivative and fullerenol, respectively [23, 24]. In addition, the fluorescence spectrum of C 60 -TEG-COOH exhibits broad fluorescence with a maximum peak at 500 nm under excitation at 350 nm, which is slightly blue-shifted compared to the fluorescence ofC 60 -TEG, meaning that the carboxylation may lead to change of the optical properties from C 60 -TEG.…”
Section: Resultsmentioning
confidence: 83%
“…The absorption spectrum shows a strong peak at 272 nm and broad bands at 300–400 nm, indicating the results from carboxylation of C 60 -TEG which has weak broad band at 260 nm and 350 nm [14]. These features are similar to those of the spectra of the hydrophilic fullerene carboxylic acid derivative and fullerenol, respectively [23, 24]. In addition, the fluorescence spectrum of C 60 -TEG-COOH exhibits broad fluorescence with a maximum peak at 500 nm under excitation at 350 nm, which is slightly blue-shifted compared to the fluorescence ofC 60 -TEG, meaning that the carboxylation may lead to change of the optical properties from C 60 -TEG.…”
Section: Resultsmentioning
confidence: 83%
“…The reaction conditions, which previously proved fruitful for us (22,36,43), gave the expected fulleropyrrolidine 1 in 25% yield. Based on previous reports, the acid hydrolysis of the acetyl groups was next carried out using an excess of p-TsOH in toluene at 90°C (44), affording 98% of the diol derivative 2. Having a proficient pathway toward the fulleropyrrolidines 1 and 2, the next step was to introduce intrinsic positive charges in both molecular structures.…”
Section: Synthesis Of the Fulleropyrrolidine Derivativesmentioning
confidence: 99%
“…125 Water soluble [60]fullerene carboxylic acid derivatives with the full 60 p-electron system have been prepared from a bis-fulleroid. 126 Fullerenols have been shown to have nitric oxide scavenging activity. 127 Fullerenols can also generate superoxide anions which result in membrane damage and cell death.…”
Section: Biologically Active Fullerenesmentioning
confidence: 99%