@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 = {://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 = {://000271603000047}, author = {Shin, J. Y. and Hepperle, S. S. and Dolphin, D.} }