Quantum yield of singlet molecular oxygen sensitization by copper(II) tetracarboxyphthalocy anine

The quantum yield φΔ for sensitization of singlet molecular oxygen, O2(1Δg), by copper(II) tetracarboxyphthalocyanine (CuTCPc) in dimethyl sulphoxide was determined under stationary illumination, using diphenyl-isobenzofurane as chemical quencher. A constant value of φΔ = 0.16 ± 0.03 was obtained, i...

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Detalles Bibliográficos
Autor principal: Lagorio, M.G
Otros Autores: Dicelio, L.E, San Román, E.A, Braslavsky, Silvia Elsa
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1989
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
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100 1 |a Lagorio, M.G. 
245 1 0 |a Quantum yield of singlet molecular oxygen sensitization by copper(II) tetracarboxyphthalocy anine 
260 |c 1989 
270 1 0 |m Braslavsky, S.E.; Max-Planck-Institut für Strahlenchemie, Stiftstrasse 34-46, D-4330 Mulheim a.d. Ruhr, Germany 
504 |a Darwent, Douglas, Harriman, Porter, Richoux, Metal phthalocyanines and porphyrins as sensitizers for reduction of water to hydrogen (1982) Coord. Chem . Rev., 44, pp. 83-126 
504 |a Wu, Zhang, Cui, Xu, Xu, A study on the ability of some phthalocyanine compounds for photogenerating singlet oxygen (1985) Acta Chim. Sinica, 1, pp. 21-25 
504 |a Ferraudi, Argüello, Ali, van Lier, Types I and II sensitized photooxidation of aminoacid by phthalocyanines: a flash photochemical study (1988) Photochem. Photobiol., 47, pp. 657-660 
504 |a Langlois, Ali, Brasseur, Wagner, van Lier, Biological activities of phthalocyanines. IV. Type II sensitized photooxidation of l-tryptophan and cholesterol by sulphonated metallophthalocyanines (1986) Photochem. Photobiol., 44, pp. 117-123. , and references cited therein 
504 |a Spikes, The historical development of ideas on applications of photosensitized reactions in the health sciences (1985) Primary Photo-Processes in Biology and Medicine, 85 A, pp. 209-227. , R.V. Bensasson, G. Jori, E. Land, T. Truscott, Plenum, New York, NATO ASI Series 
504 |a Spikes, Phthalocyanines as photosensitizers in biological systems and for the photodynamic therapy of tumors (1986) Photochem. Photobiol., 43, pp. 691-699 
504 |a Ben-Hur, Photochemistry and photobiology of phthalocyanines: new photosensitizers for photodynamic therapy of cancer (1987) From Photophysics to Photobiology, pp. 407-420. , A. Favre, R. Tyrrell, J. Cadet, Elsevier, Amsterdam 
504 |a Bernauer, Fallab, Phthalocyanine in wässeriger Lösung I (1961) Helvetica Chimica Acta, 44, pp. 1287-1292 
504 |a Darwent, Photoreduction of methyl viologen in micellar solutions sensitized by zinc phthalocyanine (1980) Journal of the Chemical Society, Chemical Communications, pp. 805-807 
504 |a Wagner, Ali, Langlois, Brasseur, van Lier, 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 Reddi, Rodgers, Spikes, Jori, The effect of medium polarity on the hematoporphyrin-sensitized photooxidation of l-tryptophan (1984) Photochem. Photobiol., 40, pp. 415-421 
504 |a Gaspard, Viovy, Agrégation de la phthalocyanine de cuivre, 4,4′,4″,4‴-tetracarboxylée en solution (1979) J. Chim. Phys., 76, pp. 571-573 
504 |a Guiraud, Foote, Chemistry of superoxide ion. III. Quenching of singlet oxygen (1976) J. Am. Chem. Soc., 98, pp. 1984-1986 
504 |a Weber, Busch, Complexes derived from strong field ligands. XIX. Magnetic properties of transition metal derivatives of 4,4′,4″,4‴-tetrasulphophthalocyanine (1965) Inorg. Chem., 4, pp. 469-471 
504 |a Achar, Fohlen, Parker, A new solid-phase polymerization —metal phthalocyanine sheet polymers (1983) J. Polym. Sci., 21, pp. 589-597 
504 |a Gaspard, Verdaguer, Viovy, Etude des phthalocyanines en solution dans l'acide sulfurique (1972) J. Chim. Phys. Phys.-chim. Biol., 69, pp. 1740-1747 
504 |a Wegner, Adamson, Photochemistry of complex ions. III Absolute quantum yields for the photolysis of some aqueous chromium(III) complexes. Chemical actinometry in the long wavelength visible region (1966) J. Am. Chem. Soc., 88, pp. 394-404 
504 |a Young, Brewer, The mechanism of quenching of singlet oxygen (1978) Singlet Oxygen. Reaction with Organic Compounds and Polymers, pp. 36-47. , B. Ranby, J.F. Rabek, Wiley, New York 
504 |a Khan, Activated oxygen Singlet molecular oxygen and superoxide anion (1978) Photochemistry and Photobiology, 28, pp. 615-627 
504 |a Krasnovsky, Jr., Photoluminescence of singlet oxygen in pigment solutions (1979) Photochemistry and Photobiology, 29, pp. 29-36 
504 |a Foote, Ching, Chemistry of 1O2. XXI. Kinetics of bilirubin photooxygenation (1975) J. Am. Chem. Soc., 97, pp. 6209-6214 
504 |a Matheson, Lee, Yamanashi, Wolbarsht, Measurement of the absolute rate constants for singlet molecular oxygen reaction with 1,3-diphenilisobenzofuran and physical quenching by ground state molecular oxygen (1974) J. Am. Chem. Soc., 96, pp. 3343-3348 
504 |a Flood, Russell, Wan, Quenching of singlet molecular oxygen by polyolefin additives in carbondisulfide solution (1973) Macromolecules, 6, pp. 669-671 
506 |2 openaire  |e Política editorial 
520 3 |a The quantum yield φΔ for sensitization of singlet molecular oxygen, O2(1Δg), by copper(II) tetracarboxyphthalocyanine (CuTCPc) in dimethyl sulphoxide was determined under stationary illumination, using diphenyl-isobenzofurane as chemical quencher. A constant value of φΔ = 0.16 ± 0.03 was obtained, independent of sensitizer concentration in the range 2-26 μM even though dimers and possibly oligomers are present at the highest concentrations. The monomer and the aggregates of CuTCPc physically quench O2(1Δg) with a nearly diffusional rate constant. © 1989.  |l eng 
536 |a Detalles de la financiación: Universidad de Buenos Aires 
536 |a Detalles de la financiación: Trimellitic anhydride was kindly provided by Dr. J. F. Sproviero (Alba, Argentina). We thank UMYMFOR (University of Buenos Aires) for the elemental analysis. M.G.L. is the recipient of a graduate student fellowship from the University of Buenos Aires. This work has been supported by research grants provided by CONICET (Consejo National de Investigaciones Cientificas y Technicas) and by the Stiftung Volkswagenwerk (F.R.G.). S.E.B. thanks the Max Planck Society for generous support and Professor K. Schaffner for his constant interest and encouragement. 
593 |a Departamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina 
593 |a Max-Planck-Institut für Strahlenchemie, Stiftstrasse 34-46, D-4330 Mulheim a.d. Ruhr, Germany 
690 1 0 |a COPPER(II) TETRACARBOXYPHTHALOCYANINE 
690 1 0 |a QUANTUM YIELD 
690 1 0 |a SINGLET MOLECULAR OXYGEN 
700 1 |a Dicelio, L.E. 
700 1 |a San Román, E.A. 
700 1 |a Braslavsky, Silvia Elsa 
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