Influence of electron-withdrawing and electron-donating substituents on photophysical properties of azaphthalocyanines
Influence of electron-withdrawing and electron-donating substituents on photophysical properties of azaphthalocyanines
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DOI：
10.1016/j.jphotochem.2006.08.024
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发表时间：
2007-02-25
影响因子：
4.3
通讯作者：
Lenco, Juraj
中科院分区：
文献类型：
--
作者：
Musil, Zbynek;Zimcik, Petr;Lenco, Juraj
New zinc azaphthalocyanines (AzaPc) were prepared using a statistical method of synthesis starting from 5,6-bis(tert-butylsulfanyl)pyrazine-2,3-dicarbonitrile (A) and 2,3-dicyano-5,6-dibutoxycarbonylpyrazine (B). All the six possible AzaPc derivatives were detected on TLC and isolated using column chromatography on silica, however, the adjacent (AABB) and opposite (ABAB) isomers were not separated. Singlet oxygen quantum yields (Phi(Delta)) were measured using the DPBF decomposition method. It was found that presence of carbonyl group bounded directly to the macrocyclic core of AzaPc slightly decreases their Phi(Delta) in dependence on the number of the butoxycarbonyl groups in succession 0.67, 0.68, 0.67, 0.59, 0.51 for AAAA, AAAB, ABAB (AABB), ABBB and BBBB type of AzaPc, respectively. Similar dependences were found in the case of fluorescence quantum yield. Conjugation of COOR group with pi-macrocyclic system leads to a somewhat bigger red-shift of the Q-band when compared with the red-shift caused by participation of lone pair of sulfur in pi-system. In contrast, the former substituents cause less hyperchromic shift at all then the tert-butylsulfanyl substituents. (c) 2006 Elsevier B.V. All rights reserved.
