| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5282813 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Orientational isomers of the octaethylporphyrin-dihexylbithiophene-pyridine system (OEP-DHBTh-Py) connected with the diacetylene linkage were synthesized. The spectral measurements were performed under neutral and acidic conditions, clearly proving that the orientation of DHBTh affects not only the electronic structures of OEP-DHBTh-Py but also their proton-mediated spectral changes.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Naoto Hayashi, Takuya Matsukihira, Keiko Miyabayashi, Mikio Miyake, Hiroyuki Higuchi,