Synthesis of stable derivatives of c(62): the first nonclassical fullerene incorporating a four-membered ring
A rational synthetic approach to the first four-membered ring-containing derivatives of C(62) is reported. They were synthesized by an inverse electron demand Diels-Alder reaction of 3,6-diaryl-1,2,4,5-tetrazines with C(60) in o-dichlorobenzene, followed by visible light irradiation at reflux. The s...
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Published in | Journal of the American Chemical Society Vol. 125; no. 8; pp. 2066 - 2067 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
26.02.2003
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Online Access | Get full text |
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Summary: | A rational synthetic approach to the first four-membered ring-containing derivatives of C(62) is reported. They were synthesized by an inverse electron demand Diels-Alder reaction of 3,6-diaryl-1,2,4,5-tetrazines with C(60) in o-dichlorobenzene, followed by visible light irradiation at reflux. The structure of these nonclassical fullerenes derivatives was determined by X-ray single-crystal diffraction. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0002-7863 |