Synthetic pathways to water-soluble phthalocyanines and close analogs - ScienceDirect Skip
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Tetrapyrrolic macrocycles have shown increasing importance in photodynamic therapy
(PDT) and diagnosis, mainly due to the possibility of fine-tuning their properties through …

Cofacial J type nano aggregates, which are both fluorescent and triplet state photoactive,
were formed in chloroform via multiple O→ Zn2+ coordination bonds between molecules of …

The excited triplet-, singlet-, and ground-state properties as well as singlet oxygen
generation capability of four brominated BODIPY dyes were measured in toluene with laser …

The stabilities of various porphin analogue compounds such as unsubstituted and
substituted phthalocyanines, tetraphenylporphyrin, naphthalocyanine and tetraazaporphyrin …

Photoactive agents based on natural products have attracted substantial attention in clinical
applications because of their distinct biological activity, molecular structure multiformity, and …

The effects of halogenation and aggregation on photosensitizing properties of zinc
phthalocyanine (ZnPC) have been examined by photophysical methods. Halogenation …

The aim of this investigation is to report the synthesis and fundamental photochemical
properties of naphthalocyanines with potential interest for photodynamic therapy (PDT), as …

Photosensitizers that selectively generate singlet oxygen in non polar/polar
microenvironments are highly desirable for photodynamic therapy of tumor but not yet …

Boron‐dipyrromethene derivatives, including cationic and iodinated analogs, were obtained
and subjected to physicochemical and in vitro photodynamic activity studies. Iodinated …