CARBOXYLATED ZINC‐PHTHALOCYANINES–II DIMERIZATION AND SINGLET MOLECULAR OXYGEN SENSITIZATION IN HEXADECYLTRIMETHYLAMMONIUM BROMIDE MICELLES

The dimerization of the diamide of zinc‐tetracarboxyphthalocyanine was studied spectro‐scopically in hexadecyltrimethylammonium bromide (CTAB) micelles at surfactant concentrations from 0.026 to 0.1 M and dye concentrations between 0.1 and 10 μM. The apparent dimerization constant in CTAB 0.1 M is 8...

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Detalles Bibliográficos
Autor principal: Daraio, Marta Edit
Otros Autores: Aramendía, P.F, San Román, E.A, Braslavsky, Silvia Elsa
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1991
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Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a cetrimide, 57-09-0, 6899-10-1, 8044-71-1; oxygen, 7782-44-7; zinc, 7440-66-6; Cetrimonium Compounds; cetrimonium, 6899-10-1; Indoles; Organometallic Compounds; Oxygen, 7782-44-7; Singlet Oxygen, 17778-80-2; zinc tetracarboxyphthalocyanine; Zinc, 7440-66-6 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
100 1 |a Daraio, Marta Edit 
245 1 0 |a CARBOXYLATED ZINC‐PHTHALOCYANINES–II DIMERIZATION AND SINGLET MOLECULAR OXYGEN SENSITIZATION IN HEXADECYLTRIMETHYLAMMONIUM BROMIDE MICELLES 
260 |c 1991 
270 1 0 |m Braslavsky, S.E. 
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504 |a Lagorio, M.G., Dicelio, L.E., San Roman, E.A., Braslavsky, S.E., Quantum yield of singlet molecular oxygen sensitization by Copper(II)‐tetracarboxy‐phthalocyanine (1989) J. Photochem. Photobiol. B: Biology, 3, pp. 615-624 
504 |a Langlois, R., Ali, H., Brasseur, N., Wagner, J.R., Van Lier, J.E., Biological activities of phthalocyanines. IV. Type II sensitized photooxidation of L‐Tryptophan and Cholesterol by sulfonated metallophthalocyanines (1986) Photochem. Photobiol., 44, pp. 117-123 
504 |a Lever, A.B.P., The phthalocyanines (1965) Adv. Inorg. Chem. Radiochem., 7, pp. 27-114 
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504 |a Moser, F.H., Thomas, A.L., (1983) The Phthalocya‐nines, 1, pp. 60-66. , CRC Press, Boca Raton, FL 
504 |a Negri, R.M., Zalts, A., San Roman, E.A., Aramen‐dia, P.F., Braslavsky, S.E., Carboxylated zinc phthalocyanines. Influence of dimerization on the spectroscopic properties. An absorption, emission, and thermal lensing study (1991) Photochemistry and Photobiology, 53, pp. 317-322 
504 |a Nonell, S., Braslavsky, S.E., Schaffner, K., Quantum yield of production of singlet molecular oxygen ('Ag) in aqueous dispersions of small unilamellar lipid vesicles. A time resolved near‐IR phosphorescence study (1990) Photochem. Photobiol, 51, pp. 551-556 
504 |a Reddi, E., Jori, G., Steady‐state and time‐resolved spectroscopic studies of photodynamic sensitizers: porphyrins and phthalocyanines (1988) Rev. Chem. Intermediates, 10, pp. 241-268 
504 |a Reynolds, W.L., Kolstad, J.J., Aggregation of 4,4′,4′,4′‐tetrasulfophthalocyanine in electrolyte solutions (1976) J. Inorg. Nucl. Chem., 38, pp. 1835-1838 
504 |a Spikes, J.D., Phthalocyanines as photosensitizers in biological systems and for the photodynamic therapy of tumors (1986) Photochem. Photobiol., 43, pp. 691-699 
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504 |a Takemura, T., Ohta, N., Nakajima, S., Sakata, I., Critical importance of the triplet lifetime of photo‐sensitizer in photodynamic therapy of tumor (1989) Photo-chem. Photobiol., 50, pp. 339-344 
504 |a Turro, N.J., Yekta, A., Luminescent probes for detergent solutions. A simple procedure for determination of mean aggregation number of micelles (1978) J. Am. Chem. Soc., 100, pp. 5951-5952 
504 |a Valduga, G., Nonell, S., Reddi, E., Jori, G., Braslavsky, S.E., The production of singlet molecular oxygen by zinc(II)‐phthalocyanine in ethanol and in unilamellar vesicles. Chemical quenching and phosphorescence studies (1988) Photochem. Photobiol., 48, pp. 1-5 
504 |a Valduga, G., Reddi, E., Jori, G., Spectroscopic studies on Zn(II)‐phthalocyanine in homogenous and microheterogeneous systems (1987) J. Inorg. Biochem., 29, pp. 59-65 
504 |a Wagner, J.R., Ah, H., Langlois, R., Brasseur, N., Van Lier, J.E., Biological‐activities of phthalocyanines. VI. Photooxidation of L‐Tryptophan by selectively sulfonated gallium phthalocyanines. Singlet oxygen yields and effect of aggregation (1987) Photochem. Photobiol., 45, pp. 587-594 
504 |a Wegner, E.E., Adamson, A.W., Photochemistry of complex ions III. Absolute quantum yields for the photolysis of some aqueous chromium (III) complexes. Chemical actinometry in long wavelength visible region (1966) J. Am. Chem. Soc., 88, pp. 394-404 
504 |a Wu, S.K., Zhang, H.C., Cui, G.Z., Xu, D.N., Xu, H.J., A study on the ability of some phthalocyanine compounds for photo‐generating singlet oxygen (1985) Act. Chim. Sinica., 43, pp. 10-13 
504 |a Yang, Y.C., Ward, J.R., Seiders, R.P., Dimerization of cobalt(II) tetrasulfonated phthalocyanine in water and aqueous alcoholic solutions (1985) Inorg. Chem., 24, pp. 1765-1769 
504 |a Zhu, Y.N., Xiao, X.R., Xu, H.J., A study of photocatalytic cleavage of water by Zinc tetracar‐boxyphthalocyanine. Ganguang Kexue Yu Kuang Huaxue 2 (1985) Photographic Sci. Photochem., 2, pp. 48-56. , (from Chem. Abstr. 132205 a, Vol. 103) 
506 |2 openaire  |e Política editorial 
520 3 |a The dimerization of the diamide of zinc‐tetracarboxyphthalocyanine was studied spectro‐scopically in hexadecyltrimethylammonium bromide (CTAB) micelles at surfactant concentrations from 0.026 to 0.1 M and dye concentrations between 0.1 and 10 μM. The apparent dimerization constant in CTAB 0.1 M is 8.6 × 105M−1, while the intramicellar dimerization constant is 1.8 × 103. The dimer absorption spectrum was also obtained. Singlet molecular oxygen sensitization was studied by steady state photolysis using 1,3‐diphenylisobenzofurane as scavenger in 0.1 M CTAB. The usual sensitization mechanism is extended to include dimer reactions. Singlet molecular oxygen sensitization yields for monomer and dimer in the micelles are 0.7 and 0.1, respectively. With the reported values it is possible to calculate the average yield of singlet molecular oxygen production at any surfactant and dye concentrations. Copyright © 1991, Wiley Blackwell. All rights reserved  |l eng 
593 |a Departamento de Química Inorgánica, Analitica Y Química Fisica, Facultad de Ciencias Exactas Y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Buenos Aires, 1428, Argentina 
593 |a Max-Planck-Institut für Strahlenchemie, Stiftstraße34-36, Mülheim A.D. Ruhr, W-4330, Germany 
650 1 7 |2 spines  |a INDOLES 
690 1 0 |a CETRIMIDE 
690 1 0 |a INDOLE DERIVATIVE 
690 1 0 |a ORGANOMETALLIC COMPOUND 
690 1 0 |a OXYGEN 
690 1 0 |a SINGLET OXYGEN 
690 1 0 |a ZINC 
690 1 0 |a ZINC TETRACARBOXYPHTHALOCYANINE 
690 1 0 |a ARTICLE 
690 1 0 |a CHEMISTRY 
690 1 0 |a MICELLE 
690 1 0 |a PHOTOCHEMISTRY 
690 1 0 |a SPECTROPHOTOMETRY 
690 1 0 |a CETRIMONIUM COMPOUNDS 
690 1 0 |a MICELLES 
690 1 0 |a ORGANOMETALLIC COMPOUNDS 
690 1 0 |a OXYGEN 
690 1 0 |a PHOTOCHEMISTRY 
690 1 0 |a SINGLET OXYGEN 
690 1 0 |a SPECTROPHOTOMETRY 
690 1 0 |a SUPPORT, NON-U.S. GOV'T 
690 1 0 |a ZINC 
700 1 |a Aramendía, P.F. 
700 1 |a San Román, E.A. 
700 1 |a Braslavsky, Silvia Elsa 
773 0 |d 1991  |g v. 54  |h pp. 367-373  |k n. 3  |p Photochem. Photobiol.  |x 00318655  |w (AR-BaUEN)CENRE-43  |t Photochemistry and Photobiology 
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