作者: S. Hagen , U. Nuechter , M. Nuechter , G. Zimmermann
DOI: 10.1080/10406639508009619
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摘要: Abstract Thermal dehydrocyclization as well isomerization reactions of 9,9′-bi-9H-fluorenylidene (2) have been investigated at temperatures above 700°C in the gas phase resulting benz[e]indeno(l,2,3-hi)acephenanthrylene(3) and dibenzo[g,p]chrysene(4), respectively. If 4 is catalytically converted, benz[g]indeno[l,2,3,4-mnop]chrysene (5) formed resonable yields by dehydrocyclization. Separate pyrolysis runs 3 5 900°C give finally diindeno[l,2,3,4-defg;1′,2′,3′,4′-mnop]chrysene (1), a bowl-shaped subunit buckminsterfullerenes, besides other polycyclic aromatic hydrocarbons.