@article {28634,
	title = {Cyclo-oligomerization of 6,12-Diethynyl Indeno[1,2-b]fluorenes via Diradical Intermediates},
	journal = {Org. Lett.},
	volume = {17},
	number = {22},
	year = {2015},
	month = {2015 NOV 20},
	pages = {5694-5697},
	type = {Article},
	abstract = {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.},
	isbn = {1523-70601523-7052},
	url = {https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b03000},
	author = {Fu, Xiangyu and <strong>Zhao, Dahui*</strong>}
}
