| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279067 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
Orientational isomers of the octaethylporphyrin-dihexylbithiophene-fullerene derivative (OEP-DHBTh-C60) connected with the diacetylene linkage were synthesized. The electronic and electrochemical properties were studied, proving that the orientation of DHBTh affects not only the electronic structures of OEP-DHBTh-C60 but also their molecular motional behaviors evidently.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Naoto Hayashi, Azusa Naoe, Keiko Miyabayashi, Mikio Miyake, Hiroyuki Higuchi,