Zinc azaphthalocyanines with thiophen-2-yl, 5-methylthiophen-2-yl and pyridin-3-yl peripheral substituents: Additive substituent contributions to singlet oxygen production
The syntheses of five pyrazine-2,3-dicarbonitriles, substituted with combinations of electron donating substituents, namely 5-methylthiophen-2-yl or thiophen-2-yl and the electron withdrawing substituent pyridin-3-yl, are reported. The compounds were obtained from the condensation of diaminomaleonit...
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Published in | Dyes and pigments Vol. 82; no. 3; pp. 276 - 285 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.09.2009
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Subjects | |
Online Access | Get full text |
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Summary: | The syntheses of five pyrazine-2,3-dicarbonitriles, substituted with combinations of electron donating substituents, namely 5-methylthiophen-2-yl or thiophen-2-yl and the electron withdrawing substituent pyridin-3-yl, are reported. The compounds were obtained from the condensation of diaminomaleonitrile and vicinal dicarbonyl compounds. Cyclotetramerizations of the monomers with both Zn(OAc)
2 and Zn(quinoline)
2Cl
2, realised substituted zinc azaphthalocyanines (ZnAzaPcs). The UV–vis spectra of these macrocycles revealed that thiophene and methylthiophene peripheral substituents induce substantial, red shifted Q-band absorptions from 636
nm for unsubstituted ZnAzaPc to 679
nm for octa(5-methylthiophen-2-yl)ZnAzaPc. This effect is substituent-specific and additive since the observed red shift for the Q-band of tetra(5-methylthiophen-2-yl)-tetra(pyridin-3-yl)ZnAzaPc is close to the calculated contribution from each substituent. Singlet oxygen quantum yields (
Φ
Δ) varied according to the peripheral substituent on ZnAzaPc and was also substituent-specific and additive. Whereas singlet oxygen production increased, the fluorescence quantum yield decreased with increasing number of substituents on ZnAzaPc; however, no quantitative relationship was found for
Φ
F and substitution patterns for the zinc complexes. Improved solubility was observed for unsymmetrical ZnAzaPcs, substituted with push–pull peripheral substituents. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0143-7208 1873-3743 |
DOI: | 10.1016/j.dyepig.2009.01.011 |