2001
DOI: 10.1002/1099-0690(200111)2001:22<4167::aid-ejoc4167>3.0.co;2-y
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The Synthesis and Characterization of Fullerene Hydrides

Abstract: The syntheses and characterization of fullerene hydrides prepared from C 60 and C 70 are reviewed. Methods of isolation and characterization are discussed, particularly MS and NMR, including 3 He nuclear magnetic resonance spectro-

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Cited by 68 publications
(56 citation statements)
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“…Experimental data confirm that more than one isomer is typically present and that the particular isomeric composition of C 60 H 36 depends on the synthesis method [11,19,20]. Mass spectral analysis of products from different hydrogenation reactions also reveals the presence of several hydrofulleride species with higher hydrogen content, such as C 60 H 38 , C 60 H 40 , and C 60 H 52 , [21][22][23] but only as minor fractions.…”
Section: Introductionmentioning
confidence: 99%
“…Experimental data confirm that more than one isomer is typically present and that the particular isomeric composition of C 60 H 36 depends on the synthesis method [11,19,20]. Mass spectral analysis of products from different hydrogenation reactions also reveals the presence of several hydrofulleride species with higher hydrogen content, such as C 60 H 38 , C 60 H 40 , and C 60 H 52 , [21][22][23] but only as minor fractions.…”
Section: Introductionmentioning
confidence: 99%
“…The synthetic approaches reported and leading to the formation of fullerene hydrides include the Birch reduction [11,15,16], the Benkeser reduction [17], polyamine reduction [18,19], reduction by diimides [20], hydroboration [21,22], hydrogen transfer reduction [7,11,23,24], photoreduction [25], transition-metal catalyzed hydrogenation [26 -28], zincconcentrated hydrochloric acid reduction [9,29,30], Zn(Cu) reduction [31][32][33], hydrozirconation [34], hydrogen radical induced hydrogenation [35], electrochemical reduction [36 -38], sonication [39], direct reduction by hydrogen [27, 40 -43], and direct exposure to atomic hydrogen [44,45]. Typically involving extreme conditions, with temperatures of several hundred Kelvin, pressures about several mega Pascal, or condensed phase condition [7,15,21,22,46], they significantly differ from the hydrogenation conditions used here and leading to the addition of up to 11 H…”
mentioning
confidence: 89%
“…As predicted by Matsuzawa et al [51] from quantum-chemical calculations, two isomers, 1 from 1,2-addition and 5 from 1,4-addition, have been synthesized [35,39]. Furthermore, isomer 1 has been synthesized by many different methods [52].…”
Section: Hydrogenation Of Fullerenementioning
confidence: 99%