Orbital - Vol. 9 No. 5 - October - December 2017
FULL PAPERS

Solvent Effect, Photochemical and Photophysical Properties of Phthalocyanines with Different Metallic Nuclei

Charles Biral Silva
Universidade Federal do ABC
Anderson Orzari Ribeiro
Universidade Federal do ABC
Hueder Paulo Moisés de Oliveira
Universidade Federal do ABC
Published December 29, 2017
Keywords
  • metallic nuclei,
  • phthalocyanines,
  • single photon counting,
  • singlet oxygen phosphorescence,
  • solvent effect
How to Cite
(1)
Silva, C. B.; Ribeiro, A. O.; de Oliveira, H. P. M. Solvent Effect, Photochemical and Photophysical Properties of Phthalocyanines With Different Metallic Nuclei. Orbital: Electron. J. Chem. 2017, 9, 344-353.

Abstract

Photophysical and photochemical properties of lithium phthalocyanine (1), gallium(III) phthalocyanine chloride (2), titanium(IV) phthalocyanine dichloride (3) and iron(II) phthalocyanine (4) were investigated in dimethyl sulfoxide (DMSO), tetrahydrofuran (THF) and DMSO-THF mixtures. The influence of the central metal on these properties was analyzed according to solvent type, axial ligands and their paramagnetic and diamagnetic effect. Fluorescence lifetimes were recorded using a time correlated single photon counting setup (TCSPC) technique. In order to demonstrate the generation of reactive oxygen species under light irradiation, the indirect method (applying 1,3-diphenylisobenzofuran (DPBF) as chemical suppressor) and the direct method (analyzing the phosphorescence decay curves of singlete oxygen at 1270 nm) were employed. Compounds 12 and showed a monomeric behavior in all media while compound 4 presented low aggregation in DMSO, but a very pronounced aggregation behavior in THF. Steady-state fluorescence anisotropy was compared with emission spectra and complex presented values beyond the expected limits.

DOI: http://dx.doi.org/10.17807/orbital.v9i5.1047