Size-selective formation of C78 fullerene from a three-dimensional polyyne precursor |
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Authors: | Tobe Yoshito Umeda Rui Sonoda Motohiro Wakabayashi Tomonari |
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Affiliation: | Division of Frontier Materials Science, Graduate School of Engineering Science, Osaka University, and CREST (JST), 1-3 Machikaneyama, Toyonaka 560-8531, Japan. tobe@chem.es.osaka-u.ac.jp |
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Abstract: | Multicyclic cagelike cyclophanes 2 a and 2 b containing cyclobutene rings have been prepared as precursors of three-dimensional polyynes C78H18 (1a) and C78H12Cl6 (1b), respectively. Laser irradiation of 2a and 2b induced expulsion of the aromatic fragment, indane, to give the three-dimensional polyyne anions C78H18- and C78H12Cl6-, respectively. Whereas the former anion lost only four hydrogen atoms to form C78H14-, complete loss of all hydrogen and chlorine atoms was observed from the latter anion, to yield a C78- ion that has a fullerene structure which was proven by its characteristic fragmentation pattern. |
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Keywords: | alkynes cyclophanes fullerenes macrocycles polycycles |
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