Cyclo-oligomerization of 6,12-Diethynyl Indeno[1,2-b]fluorenes via Diradical Intermediates

摘要:

Indeno[1,2-b]fluorene derivatives with trimethlysilylethynyl substituents at the 6- and 12-positions were found to undergo cyclo-dimeerzatin cyclo-trimaerzatio and higher oligomerization at room tempeatrue. The cyclic dimer feature a novel double-decker motif, composed of two face-to-face stacked bis(propadienylide)dihydroindeno[1,2-b] flourenes with a short centroid-to- centroid distance of 3.50 angstrom. The existence of a cyclic timer and higher oligemers was indeno[1,2-b]fluorene moiety.

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