When 1-(pentaphenylphenyl)-2-phenylacetylene (1) is heated with (eta(5)-cyc
lopentadienyl)dicarbonylcobalt, 1,2,3,4-tetraphenylfluorene (3) and related
minor products are formed rather than the expected tetraaryl-cyclobutadien
e. The formation of 3 requires that a seven-carbon fragment (formally a phe
nylcarbyne) must be lost. Two minor products, however, result from intramol
ecular cyclization of the alkyne and these two retain all of the carbons fr
om the starting material. (C) 2000 Elsevier Science Ltd. All rights reserve
d.