@conference {9822,
	title = {Synthesis of di-phenyl-conjugated azadipyrromethene and its BF2 complex.},
	year = {2010},
	note = {CAPLUS AN 2010:345548(Conference; Meeting Abstract; Computer Optical Disk)},
	month = {2010///},
	pages = {ORGN-270},
	publisher = {American Chemical Society},
	organization = {American Chemical Society},
	abstract = {Azadipyrromethenes are the bridged nitrogen analogs of dipyrromethenes. Since they were considered as potential photosensitizers for photodynamic therapy, the synthesis of tetraarylazadipyrromethene-BF2 complexes has attracted the interest of several research groups. However, X-ray crystallog. anal. of the parent chromophore, 3,3{\textquoteright},5,5{\textquoteright}-tetraphenyl-azadipyrromethene-BF2 complex, showed that none of the four Ph groups were effectively conjugated with the core plane of the azadipyrromethene-BF2 complex. This finding drew our attention to explore the synthesis of Π-conjugated azadipyrromethene-BF2 complexes, and the visible max. absorption of BF2 complex of indol-2-yl-isoindol-1-ylidene-amine (3) has reached to 528 nm. [on SciFinder(R)]},
	author = {Li,Yan and Dolphin,David and Patrick,Brian O.}
}
