@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 {2599,
	title = {Linear fully conjugated meso-aryl pentapyrrins},
	journal = {Tetrahedron Letters},
	volume = {50},
	number = {49},
	year = {2009},
	note = {ISI Document Delivery No.: 517HDTimes Cited: 0Cited Reference Count: 34Shin, Ji-Young Hepperle, Steven S. Dolphin, David},
	month = {Dec},
	pages = {6909-6912},
	type = {Article},
	abstract = {A meso-2,6-dichlorophenyl pentapyrrin was prepared using a modified method for dipyrrane synthesis followed by simple DDQ oxidation. The fully conjugated structures formed via redox inter-conversions were studied using crystallographic as well as observed and calculated spectral data. (C) 2009 Elsevier Ltd. All rights reserved.},
	keywords = {ANISOTROPIC DIELECTRICS, AROMATICITY, BASIS-SET, DENSITY-FUNCTIONAL THEORY, EXPANDED, IMPLEMENTATION, macrocycles, MESOSUBSTITUTED DIPYRROMETHANES, MOLECULAR-ORBITAL METHODS, porphyrins, TRIPYRRANE},
	isbn = {0040-4039},
	url = {<Go to ISI>://000271603000047},
	author = {Shin, J. Y. and Hepperle, S. S. and Dolphin, D.}
}
