Synthesis and photophysical studies of monocarboxy phthalocyanines containing quaternizable groups

Yasin Arslanoğlu, Tebello Nyokong*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

This work reports on the synthesis and photophysical properties of novel unsymmetrically substituted monocarboxy magnesium (MgPc, 3), aluminum (ClAlPc, 4) and unmetallated (H2Pc, 5) phthalocyanines. Magnesium phthalocyanine (3) was converted into water soluble quaternized derivative (QMgPc, 6) by reaction with methyl iodide. The synthesized phthalocyanines were characterized by IR, UV-Vis, NMR, mass spectrometry and elemental analyses. Photophysical and photochemical studies were carried out in order to determine the potential of the complexes as photosensitizers for use in photodynamic therapy. Triplet quantum yields ranged from 0.37 to 0.40 and triplet lifetimes from 110 to 140 μs in DMSO.

Original languageEnglish
Pages (from-to)2733-2739
Number of pages7
JournalPolyhedron
Volume30
Issue number16
DOIs
Publication statusPublished - 11 Oct 2011

Funding

This work was supported by the Department of Science and Technology (DST) and National Research Foundation (NRF), South Africa through DST/NRF South African Research Chairs Initiative for Professor of Medicinal Chemistry and Nanotechnology as well as Rhodes University. Y.A. thanks to Istanbul Technical University, DPT and TUBITAK.

FundersFunder number
DST/NRF
National Research Foundation
Rhodes University
Department of Science and Technology, Government of Kerala

    Keywords

    • Fluorescence
    • Metallophthalocyanine
    • Triplet yield
    • Water soluble

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