2006
DOI: 10.1016/j.jphotochem.2006.03.024
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Differently substituted phthalocyanines: Comparison of calculated energy levels, singlet oxygen quantum yields, photo-oxidative stabilities, photocatalytic and catalytic activities

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Cited by 89 publications
(44 citation statements)
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“…One important property of phthalocyanines under irradiation in the absorption region is photosensitized generation of singlet oxygen [4,5,12,19,25]. In the present study, singlet oxygen quantum yields of dinuclear phthalocyanines Zn2, Zn3 and H 2 2 were measured and compared to the quantum yields of their mononuclear analogs H 2 1 and Zn1 and zinc tetra-tertbutylnaphthalocyanine Zn4 (literature value 0.41 [19]).…”
Section: Resultsmentioning
confidence: 98%
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“…One important property of phthalocyanines under irradiation in the absorption region is photosensitized generation of singlet oxygen [4,5,12,19,25]. In the present study, singlet oxygen quantum yields of dinuclear phthalocyanines Zn2, Zn3 and H 2 2 were measured and compared to the quantum yields of their mononuclear analogs H 2 1 and Zn1 and zinc tetra-tertbutylnaphthalocyanine Zn4 (literature value 0.41 [19]).…”
Section: Resultsmentioning
confidence: 98%
“…Singlet oxygen quantum yields were measured as described elsewhere [19,25]. Photosensitizer concent rations corresponding to an optical density of 0.2 at the Q-band maximum was used (0.74 mM of Zn1, 0.54 mM of Zn2, 0.37 mM of Zn3, or 0.50 mM of Zn4).…”
Section: Methodsmentioning
confidence: 99%
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“…Preparation of FePc(COOH) 4 and FePc(COOH) 4 /TiO 2 The synthesis of Fe (III) 2, 9, 16, 23-phthalocyanine tetracarboxylic acid (FePc(COOH) 4 ).FeCl 3 ⋅6H 2 O, urea, and trimellitic anhydride (molar ratio=0.25:20:1) were used as the raw materials to prepare FePc(COOH) 4 by a solid fusion method, and the product was purified [22].…”
Section: Methodsmentioning
confidence: 99%
“…It is well known that modifications on the MPc by introducing peripheral substituents and axial ligands can strongly influence and finally tune the solubility, photocatalytic, electrochemical, optical, conductive, etc. properties of the MPcs complexes [1]- [4]. The axial substitution produces relevant changes on the electronic structure of the molecule, in particular the pi-electronic distribution, as a consequence of changes in the spin density and dipole moment of the central metal-axial ligand bonds [5].…”
Section: Introductionmentioning
confidence: 99%