1996
DOI: 10.1016/0040-4020(96)00103-2
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Fullerenes by pyrolysis of hydrocarbons and synthesis of isomeric methanofullerenes

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Cited by 59 publications
(27 citation statements)
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“…Fig. 23) [97][98][99][100], the sodium fullero cryptate 90 ( Fig. 23) [101], and fullerene azacrown ethers 91-95 ( Fig.…”
Section: Fullerene Crown Ethersmentioning
confidence: 99%
“…Fig. 23) [97][98][99][100], the sodium fullero cryptate 90 ( Fig. 23) [101], and fullerene azacrown ethers 91-95 ( Fig.…”
Section: Fullerene Crown Ethersmentioning
confidence: 99%
“…Such arrays display interesting photophysical [2,3] and electrochemical properties [4,5] with broad application potential. The linker moiety is used for attaching the crown ether moiety onto the fullerene core through standard reaction protocols, including 1,3-dipolar cycloaddition with azomethine ylides [2,12] or diazomethane derivatives, [10,18] [4+2] cycloaddition with dienes [4] or quinodimethane precursors, [3,7] and the Bingel reaction with malonates (Scheme 1). [6][7][8][9] Furthermore, crown ether tagged fullerenes have been used for exploring the chemistry of C 60 by electrospray mass spectrometry.…”
mentioning
confidence: 99%
“…For example, it has been shown that the cationbinding-dependant changes in their redox potential and fluorescence quenching may find applications in specific ion sensors and fluorescence switching devices, respectively. The linker moiety is used for attaching the crown ether moiety onto the fullerene core through standard reaction protocols, including 1,3-dipolar cycloaddition with azomethine ylides [2,12] or diazomethane derivatives, [10,18] [4+2] cycloaddition with dienes [4] or quinodimethane precursors, [3,7] and the Bingel reaction with malonates (Scheme 1). [10] More importantly, the covalent linkage of a crown ether moiety on the fullerene core is a unique approach to the construction of functional supramolecular fullerene assemblies, [11] such as exTTF-C 60 dyads (exTTF = p-extended tetrathiafulvalene), [12] self-assembled carbon nanotube/fullerene donor-acceptor hybrids, [13] fullerene dimers, [14] [60]fullerene-based rotaxanes, [15] fullerene-based thin films formed by self-assembled monolayers (SAMs) of C 60 , [16] as well as Langmuir-Blodgett films.…”
mentioning
confidence: 99%
“…Mostly helium with optimized pressure is used. They can also be manufactured by heating carbon black with an optimized flame [65][66][67]. Afterward, the carbon black gets extracted with organic solvents (e. g., toluene, resulting in a yield of 10 to 15% fullerenes); the amount of C 60 is greatest, 80%, whereas C 70 has a yield of 15%, the rest being the higher fullerenes up to C 94 [68,69].…”
Section: Derivatized Fullerenesmentioning
confidence: 99%