Low-temperature luminescence of purine derivatives: Salt effects

Xanthines (caffeine, theophylline and theobromine) and purine have very low quantum yields of fluorescence in ethanol and acetonitrile solutions at room temperature (Φf < 10-3; naphthalene as fluorescence reference). At 77 K xanthines show good fluorescence and phosphorescence spectra, while...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autor principal: Murgida, D.H
Otros Autores: Erra-Balsells, R.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier 1999
Acceso en línea:Registro en Scopus
DOI
Handle
Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
LEADER 07430caa a22009377a 4500
001 PAPER-2483
003 AR-BaUEN
005 20230518203152.0
008 190411s1999 xx ||||fo|||| 00| 0 eng|d
024 7 |2 scopus  |a 2-s2.0-0008625626 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JLUMA 
100 1 |a Murgida, D.H. 
245 1 0 |a Low-temperature luminescence of purine derivatives: Salt effects 
260 |b Elsevier  |c 1999 
270 1 0 |m Erra-Balsells, R.; Depto. de Quim. Orgánica, Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, c.c.74-suc. 30, 1430-Buenos Aires, Argentina; email: erra@qo.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Robinson, T., (1968) The Biochemistry of Alkaloids, , Springer, New York 
504 |a Kasama, K., Takematsu, A., Arai, S., (1982) J. Phys. Chem., 86, p. 2420 
504 |a Andino, M.M., Lima, C.G., Winefordner, J.D., (1987) Spectrochim. Acta A, 43, p. 427 
504 |a Cadet, J., Berger, M., Buchko, G.W., Joshi, P.C., Raoul, S., Ravanat, J.R., (1994) J. Am. Chem. Soc., 116, p. 7403 
504 |a Morin, B., Cadet, J., (1994) Photochem. Photobiol., 60, p. 102 
504 |a Armitage, B., Yu, Ch., Devadoss, Ch., Schuster, G.B., (1994) J. Am. Chem. Soc., 116, p. 9847 
504 |a Görner, H., (1994) J. Photochem. Photobiol., B: Biology, 26, p. 117 
504 |a Bonesi, S.M., Erra-Balsells, R., (1999) An. Asoc. Quimica Argentina, 87, p. 127 
504 |a Biondic, M.C., Erra-Balsells, R., (1998) J. Chem. Res. (S), p. 114 
504 |a Nonami, H., Tanaka, K., Fukuyama, Y., Erra-Balsells, R., (1998) R. Comm. Mass Spectrometry, 12, p. 285 
504 |a Murgida, D.H., Erra-Balsells, R., Bilmes, G.M., (1996) Chem. Phys. Lett., 250, p. 198 
504 |a Murgida, D.H., Bilmes, G.M., Erra-Balsells, R., (1996) Photochem. Photobiol., 64, p. 777 
504 |a Murgida, D.H., Aramendía, P.F., Erra Balsells, R., (1998) Photochem. Photobiol., 67, p. 487 
504 |a Murgida, D.H., Aramendía, P.F., Erra Balsells, R., (1998) Photochem. Photobiol., 68, p. 467 
504 |a Murgida, D.H., Erra Balsells, R., Crippa, P.R., Viappiani, C., (1998) Chem. Phys. Lett., 294, p. 538 
504 |a Drobnik, J., Augenstein, L., (1966) Photochem. Photobiol., 5, p. 13 
504 |a Drobnik, J., Augenstein, L., (1966) Photochem. Photobiol., 5, p. 83 
504 |a Drobnik, J., Kleinwächter, V., Augenstein, L., (1967) Photochem. Photobiol., 6, p. 147 
504 |a Longworth, J.W., Rahn, R.O., Schulman, R.G., (1966) J. Phys. Chem., 45, p. 2930 
504 |a Daniels, M., Hauswirth, W., (1971) Science, 171, p. 675 
504 |a Aaron, J.J., Winefordner, J.D., (1973) Photochem. Photobiol., 18, p. 97 
504 |a Smith, J.J., (1976) Photochem. Photobiol., 23, p. 365 
504 |a Moller, G., Nishimura, A.M., (1977) J. Phys. Chem., 81, p. 147 
504 |a Gibson, E.P., Turnbull, J.H., (1979) J. Photochem., 11, p. 313 
504 |a Wilson, R.W., Callis, P.R., (1980) Photochem. Photobiol., 31, p. 323 
504 |a Tohara, A., Hirakawa, A.Y., (1980) Chem. Phys. Lett., 75, p. 145 
504 |a Knighton, W.B., Giskaas, G.O., Callis, P.R., (1982) J. Phys. Chem., 86, p. 49 
504 |a Börrensen, H.C., (1963) Acta Chem. Scand., 17, p. 921 
504 |a Parkanyi, C., Bouin, D., Shich, D.C., Tunbrant, S., Aaron, J.J., Tine, A., (1984) J. Chim. Phys., 81, p. 21 
504 |a Gaye, M.D., Aaron, J.J., (1988) Anal. Chim. Acta, 205, p. 273 
504 |a Gaye, M.D., Aaron, J.J., (1989) Talanta, 36, p. 445 
504 |a Gaye, M.D., Delamar, M., Aaron, J.J., (1990) Analusis, 18, p. 571 
504 |a Lukasiewicz, R.J., Mousa, J.J., Winefordner, J.D., (1972) Anal. Chem., 44, p. 963 
504 |a Zahalka, J., Donbrow, M., Yanuka, Y., (1993) J. Chem. Res. (S), p. 351 
504 |a Yanuka, Y., Zahalka, J., Donbrow, M., (1986) J. Chem. Soc. Perkin Trans. II, p. 911 
504 |a Kapuscinski, J., Kimmel, M., (1993) Biophys. Chem., 46, p. 153 
504 |a Vo-Dinh, T., (1984) Room Temperature Phosphorimetry for Chemical Analysis, , P.J. Elving, J.D. Winefordner (Eds.), Wiley, New York 
504 |a Turro, N.J., (1978) Modern Molecular Photochemistry, , The Benjamin/Cumming Publishing Co., New York 
504 |a Murov, S.L., Carmichael, I., Hug, G.L., (1993) Handbook of Photochemistry, , Marcel Dekker, New York 
504 |a Arce, R., Jimenez, L.A., Rivera, V., Torres, C., (1980) Photochem. Photobiol., 32, p. 91 
504 |a Norrish, R.G.W., Porter, G., (1949) Nature, 164, p. 658 
504 |a Quinones, E., Arce, R., (1989) J. Am. Chem. Soc., 111, p. 8218 
520 3 |a Xanthines (caffeine, theophylline and theobromine) and purine have very low quantum yields of fluorescence in ethanol and acetonitrile solutions at room temperature (Φf < 10-3; naphthalene as fluorescence reference). At 77 K xanthines show good fluorescence and phosphorescence spectra, while purine only shows phosphorescence. Working at low temperature, the effect of the properties of the solid matrix (solvent composition and the presence of inorganic salts) on the emission spectra were studied. It was observed that the addition of inorganic salts changes the optical properties of the matrix (snowed matrix, cracked matrix, etc.) as well as produces heavy atom effect. These effects are opposite in the case of fluorescence, but are co-operative for phosphorescence. © 1999 Elsevier Science B.V. All rights reserved.  |l eng 
536 |a Detalles de la financiación: Ehime University 
536 |a Detalles de la financiación: Universidad de Buenos Aires, TW-34 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas, PIP 1998-2000 
536 |a Detalles de la financiación: The authors thank University of Buenos Aires (TW-34) and CONICET (PIP 1998-2000) for partial financial support and Dr. Hiroshi Nonami (College of Agriculture, Ehime University, Japan) for some chemicals. REB is a member of Carrera del Investigador Cientı́fico of Consejo Nacional de Investigaciones Cientı́ficas y Técnicas (CONICET). 
593 |a Depto. de Quim. Orgánica, Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, c.c.74-suc. 30, 1430-Buenos Aires, Argentina 
690 1 0 |a CAFFEINE 
690 1 0 |a LOW TEMPERATURE LUMINESCENCE 
690 1 0 |a PURINES 
690 1 0 |a THEOBROMINE 
690 1 0 |a THEOPHYLLINE 
690 1 0 |a XANTHINES 
700 1 |a Erra-Balsells, R. 
773 0 |d Elsevier, 1999  |g v. 85  |h pp. 129-136  |k n. 1-3  |p J Lumin  |x 00222313  |w (AR-BaUEN)CENRE-571  |t Journal of Luminescence 
856 4 1 |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-0008625626&doi=10.1016%2fS0022-2313%2899%2900059-9&partnerID=40&md5=4c52f03cddf6b8580e9025dec7d70244  |y Registro en Scopus 
856 4 0 |u https://doi.org/10.1016/S0022-2313(99)00059-9  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00222313_v85_n1-3_p129_Murgida  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00222313_v85_n1-3_p129_Murgida  |y Registro en la Biblioteca Digital 
961 |a paper_00222313_v85_n1-3_p129_Murgida  |b paper  |c PE 
962 |a info:eu-repo/semantics/article  |a info:ar-repo/semantics/artículo  |b info:eu-repo/semantics/publishedVersion 
999 |c 63436