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• Claessens, Torres, T., "Singular Nonplanar Aromatic Compounds-Synthesis, Reactivity, and Physical Properties”, Chem. Rev, 102, 835-853,(2002).
• Zdravkovski, D., Milletti, M.C., “A comparison of structural and electronic characteristics among subphthalocyanine and phthalocyanine complexes”, Journal of Molecular structure: THEOCHEM, 717, 85-89, (2005).
• Kobayashi, N., Kondo, R., Nakayama, T., Osa, T., “Near-infrared absorbing dyes”, Review, J.Am.Chem.Soc. 112, 9640, (1990).
• Gong, X.D., Xiao, H.M., Gao, P., Tian, H.,“A density functional theory study of the structure and subphthalocyanines”, Journal of Molecular structure: THEOCHEM, 587, 189-197, (2002). Matlaba, substituents and solvents on the photochemical properties of zinc phthalocyanine complexes and their protonated derivatives “, Polyhedron, 2463-2472, (2002). T., “Effects of
• González-Rodríguez, D., Torres, T., Guldi, D.M., Rivera, J., Echegoyen, L. "Energy transfer processes in novel subphthalocyanine- fullerene ensembles”, Organic Letters, Vol:4, No:3, 335-338, (2002).
• Spesia, M.S., Durantini, E.N., “Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative “, Dyes and Pigments, 229-237, (2008). Scalise, properties, and photodynamic inactivation of E.N., “Synthesis,
• Escherichia coli using a cationic and a noncharged Zn(II) pyridyloxyphthalocyanine derivatives Chemistry, 13, 3037-3045 (2005).
• Ackroyd, R., Kelty, C., Brown, N., Reed, M., “The photodynamic therapy”, Photochem. Photobiol. 74, 656-669 (2001). and Lang, K., Mosinger, J., Wagnerova, D.M.,
• “Review;Photophysical porphyrinoid sensitizers non-covalently bound to host molecules; models for photodynamic therapy “, Coordination Chem. Reviews, 248, 321- 350, (2004). properties of
• Macdonald, I.J., Dougherty, T.J., “Basic principles J.Porphyrins&Phthalocyanines, 5, 105-129, (2001). therapy”,
• Kantonis, G.; Trikeriotis, M.; Ghanotakis, D.F., with “The antimicrobial photodynamic therapy”, J. Photochem. Photobiol. A: Chem., 185, 62-66, (2007). in
• Atilla, D., Durmus, M., Yılmaz, Gürek, A.G., Ahsen V. and Nyokong, T., “Synthesis, Photophysical and Photochemical Properties of Poly(oxyethylene) Phthalocyaninato oxotitanium(IV) Complexes”, Eur. J. Inorg. Chem., 3573-3581, (2007). New
• Kassab, K., Fabris, C., Defilippis, M.P., Dei, D., Fantetti, L., Roncucci, G., Reddi, E., Jori, G., “Skin-photosensitizing properties of Zn(II)-2(3), 9(10), methylpiperidinyl) administered J.Photochem.Photobiol.B:Biol. 55, 128-137, (2002). topically mice.”, to
• Pandey, R.K. , “Photo physical and biological characteristics of metallo- phthalocyanines for applications J.Porphyrins&Phthalocyanines, 4, 368-373, (2000). PDT”,
• Peeva, M., Shopova, M., Michelsen, U., Wörhle, D., Petrov, G., Diddens, H., “In vitro and in- vivo benzonaphthoporphyrazines as photosensitizers for PDT”, J.Porphyrins & Phthalocyanines, 5, 645-651, (2001). cationic Zn(II)
• Sakamoto, K., Kato, T., Kawaguchi, T., Ohno- Okumura, E., Urano, T., Yamaoka, T., Suzuki, S., Cook, M.J., “Photosensitizer efficacy of non- peripheral alkylbenzopyridoporphyrazines photodynamic therapy of cancer”, J. Photochem. Photobiol. A: Chem., 153, 245-253, (2002). for
• Nakae, Y., Fukusaki, E.-i., Kajiyama, S.-i., Kobayashi, A., Sakata, I., “Convenient screening methods for the photosensitivity”, J. Photochem. Photobiol. A: Chem., 171, 91-95, (2005).
• Giuntini, F.; Raoul, Y.; Dei, D.; Municchi, M.; Chiti, G. ; Fabris, C.; Colautti, P.; Jori, G.; Roncucci, G.,” Synthesis of tetrasubstituted Zn(II)-phthalocyanines carboranyl-units as potential BNCT and PDT agents “, Tetrahedron letters, 46, 2979-2982, (2005). carrying four
• Kudrevich, S., Brasseur, N., La Mandeleine, C., Gilbert, S., van Lier, J.E., “Studies on the synthesis phthalocyanines macrocyclic moieties”, J. Med. Chem., 40, 3897-3904, (1997). of novel donor mixed
• Gabor, F.; Csik, G.; Ronto, G., “Photodynamic therapy: a new antimicrobial approach”, Med. Sci Monit., 3(3), 294-298, (1997).
• Mantavera, V., Kussovski, V., Angelov, I., Borisova, E., Avramov, L., Schnurfeil, G., Wöhrle, D., “Photodynamic activity of water- soluble phthalocyanine zinc(II) complexes against &Bioorganic&&&&Med. Chem., 15, 4829-4835, (2007). microorganisms”,
• Kaliya, O.L., Lukyanets, E.A., Vorozhtsov, G.N., A. A. Pashkovskaya, I. V. Perevoshchikova, V. E. Maizlish, G. P. Shaposhnikov, E. A. Kotova and Yu. N. Antonenko , “Interaction of tetrasubstituted phthalocyanine with artificial and natural membranes”, Phthalocyanines, 3, 592-610, (1999). J.Porphyrins &
• (a) Bonnet, R., Martinez, G., « Tetra sulfunated phthalocyanine nickel Tetrahedron, 57, 9513-9547, (2001). (b)
• O’Riordan, K.; Akilov, O.E.; Hasan, T., “The potential for photodynamic therapy in the treatment Photodiagnosis and Photodynamic Therapy, 2, 247-262, (2005). assemblies”, of infections” ,
• Minnock, A.; Vernon, D. I.; Schofield, J.; Griffiths, J. ; Parish, J.H.; Brown, S.B., “Photoinactivation of bacteria. Use of a cationic water photoinactivate both gram-negative and gram- positive bacteria.”, J. Photochem. Photobiol. B: Biol. 32, 159-164,(1996). to
• Minnock, A., Vernon, D. I., Schofield, J., Griffiths, J., Parish, J.H., Brown, S.B., “Photodynamic proposed as a potentially topical, non-invasive approach suitable proliferating neoplastic cells”, Antimicrob. Agents Chemother. 44 (3) 522- 527, (1996). therapy is
• Lacey, J.A., Phillips, D., “The photosensitisation coli of Escherichia using disulphonated aluminium phthalocyanine”, J. Photochem. Photobiol. A: Chem., 142, 145-150, (2001).
• Dupouy, E.A., Lazzeri, D., Durantini, E.N., “Photodynamic activity of cationic Pcs on E- coli”, J. Photochem. Photobiol., Sci. 3, 992- 998, (2004).
• Humberstone, P., Clarkson, G. J,. McKeown, N. B. and Treacher, K. E., “Synthesis and liquid crystal properties of phthalocyanine derivatives containing both alkyl and readily oxidised phenolic substituents”, J. Mater. Chem., 6, 315- 322, (1996).
• Clarkson, G.J., Humberstone, P., Mckeown, N.B., “Synthesis of a Phthalocyanine Derivative Containing Easily Oxidized Sterically Hindered Phenolic Substituents”, Chem. Commun, 1979- 1980, (1997).
• Yang JG, Onyebuagu W., “Synthesis and characterization phthalocyanines”, J Org Chem, 55, 2155, (1990). disubstituted
• Yukruk, F., Dogan, A.L., Canpinar, H., Guc, D., Akkaya, E.U., “(PDI) Dyes as Potential Sensitizers for Photodynamic Therapy”, Org. Lett. 7(14), 2885-2887, (2005).
• Seven, O., Dindar, B.,Aydemir, S., Cilli, F., properties “"Synthesis, activities of some Zinc(II) phthalocyanines against Escherichia coli and Staphylococcus aureus”, J.Porphyrins & Phthalocyanines, 12(8), 953-963, (2008). and photodynamic