| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1530795 | Materials Science and Engineering: B | 2009 | 4 Pages |
Abstract
In this study, an unsymmetrical phenanthroline-appended azaphthalocyanine with a completely planar conjugated molecular structure was synthesized. 1H NMR spectroscopy confirmed its structure. Electronic absorption characterization showed that the Q-band absorption of phthalocyanine was significantly broadened and red-shifted due to extended π-conjugation, and mid-wavelength light could also be well absorbed due to phenanthroline component. such a panchromatic ligand bears peripheral chelating site and can further form metal complex dyads.
Related Topics
Physical Sciences and Engineering
Materials Science
Electronic, Optical and Magnetic Materials
Authors
Yizhu Liu, Hong Lin, Jianbao Li, Kai He,