Sakamoto, Keiichi, Ohno-Okumura, Eiko, Kato, Taku, Watanabe, Masaki and Cook, Mike (2008) Investigation of zinc bis(1,4-didecylbenzo)-bis(2,3-pyrido) porphyrazine as an efficient photosensitizer by cyclic voltammetry. Dyes and Pigments, 78 (3). pp. 213-218.
Full text not available from this repository.Abstract
The phthalocyanine analogue containing non-peripheral, long alkyl-substituted benzenoid rings and pyridine rings, zinc bis(1,4-didecylbenzo)-bis(2,3-pyrido)porphyrazine was synthesized. The synthesized product is an interesting compound because quaternization of the pyridine nitrogen is expected to impart cationic amphiphilic character. Zinc bis(1,4-didecylbenzo)-bis(2,3-pyrido)porphyrazine was reacted with dimethyl sulfate and monochloroacetic acid to produce the quaternized products and with diethyl sulfate to produce the sulfo-substituted product; all such compounds displayed amphiphilic character. Identical peaks in cyclic voltammograms were obtained for the products before and after quaternization. Zinc bis(1,4-didecylbenzo)-bis(2,3-pyrido)porphyrazine had no changes in its reduction or oxidation properties compared to phthalocyanine analogues.
Item Type: | Article |
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Faculty \ School: | Faculty of Science > School of Chemistry (former - to 2024) |
Depositing User: | Rachel Smith |
Date Deposited: | 22 Mar 2011 13:14 |
Last Modified: | 24 Sep 2024 09:35 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/26877 |
DOI: | 10.1016/j.dyepig.2007.12.004 |
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