@article {2602,
	title = {BODIPY-Hexaphyrin Hybrids},
	journal = {Chemistry-a European Journal},
	volume = {15},
	number = {47},
	year = {2009},
	note = {ISI Document Delivery No.: 544YKTimes Cited: 2Cited Reference Count: 33Shin, Ji-Young Tanaka, Takayuki Osuka, Atsuhiro Miao, Qing Dolphin, David},
	pages = {12955-12959},
	type = {Article},
	keywords = {AROMATICITY, BODIPY, CHEMISTRY, DYES, electron transfer, EXPANDED PORPHYRIN, hexaphyrin, MESO-HEXAKIS(PENTAFLUOROPHENYL), MOBIUS AROMATICITY, SUBSTITUTED EXPANDED PORPHYRINS},
	isbn = {0947-6539},
	url = {<Go to ISI>://000273697100008},
	author = {Shin, J. Y. and Tanaka, T. and Osuka, A. and Miao, Q. and Dolphin, D.}
}
@article {3293,
	title = {CHARACTERIZATION OF DECAMETHYL AND ETHOXYCARBONYL PENTAPHYRINS},
	journal = {Heterocycles},
	volume = {41},
	number = {11},
	year = {1995},
	note = {ISI Document Delivery No.: TF562Times Cited: 5Cited Reference Count: 23},
	month = {Nov},
	pages = {2553-2564},
	type = {Article},
	abstract = {The syntheses of decamethyl- and ethoxycarbonyl-pentaphyrins are described. Their spectroscopic characterizations are presented in comparison with the permethyl derivatives of porphyrin, sapphyrin and hexaphyrin. The ethoxycarbonyl containing pentaphyrins are the only examples, amongst the expanded polypyrrolic macrocycles, that have an electron withdrawing group directly attached to the macrocyclic ring system. Elimination of a pyrrole and methine carbon unit in the mass spectrometer has been observed as a common feature for the pentaphyrin free bases as well as their metal derivatives.},
	keywords = {COMPLEX, EXPANDED PORPHYRIN, macrocycles, SAPPHYRINS},
	isbn = {0385-5414},
	url = {<Go to ISI>://A1995TF56200017},
	author = {Dansodanquah, R. E. and Xie, L. Y. and Dolphin, D.}
}
