| Title | Linear fully conjugated meso-aryl pentapyrrins |
| Publication Type | Journal Article |
| Year of Publication | 2009 |
| Authors | Shin, JY, Hepperle, SS, Dolphin, D |
| Journal | Tetrahedron Letters |
| Volume | 50 |
| Pagination | 6909-6912 |
| Date Published | Dec |
| Type of Article | Article |
| ISBN Number | 0040-4039 |
| Keywords | ANISOTROPIC DIELECTRICS, AROMATICITY, BASIS-SET, DENSITY-FUNCTIONAL THEORY, EXPANDED, IMPLEMENTATION, macrocycles, MESOSUBSTITUTED DIPYRROMETHANES, MOLECULAR-ORBITAL METHODS, porphyrins, TRIPYRRANE |
| 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. |
| URL | <Go to ISI>://000271603000047 |
