A luminescent steroid-based organogel: ON-OFF photoswitching by dopant interplay and templated synthesis of fluorescent nanoparticles

The modulation of the fluorescence emission of a perylene dye between ON and OFF states was achieved with high efficiency by means of a diarylethene photochromic compound in an organogel medium. Fluorescent gels were prepared from a steroidal low molecular weight organogelator doped with the perylen...

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Autor principal: Edelsztein, V.C
Otros Autores: Jares-Erijman, E.A, Müllen, K., Di Chenna, P.H, Spagnuolo, C.C
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2012
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 Edelsztein, V.C. 
245 1 2 |a A luminescent steroid-based organogel: ON-OFF photoswitching by dopant interplay and templated synthesis of fluorescent nanoparticles 
260 |c 2012 
270 1 0 |m Di Chenna, P.H.; UMYMFOR(CONICET-UBA), Facultad de Ciencias Exactas y Natura-les, Dto. Química Orgánica, 3er piso Pabe-llón II, Cdad. Universitaria, Buenos Aires, Argentina; email: dichenna@qo.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Das, D., Kar, T., Das, P.K., (2012) Soft Matter, 8, p. 2348 
504 |a Steed, J.W., (2011) Chem. Commun., 47, p. 1379 
504 |a Ajayaghosh, A., Praveen, V.K., Vijayakumar, C., (2008) Chem. Soc. Rev., 37, p. 109 
504 |a Huebon, F.J.M., Jonkheijim, P., Meijer, E.W., Schenning, A.P.H.J., (2005) Chem. Soc. Rev., 105, p. 1491 
504 |a Li, X., Peng, J., Kang, J., Choy, J., Steinhart, M., Knoll, W., Kim, D., (2008) Soft Matter, 4, p. 515 
504 |a Sada, K., Takeuchi, M., Fujita, N., Numata, M., Shinkai, S., (2007) Chem. Soc. Rev., p. 415 
504 |a Yagai, S., Ishii, M., Karatsu, T., Kitamura, A., (2007) Angew. Chem., Int. Ed., 46, p. 1 
504 |a Huang, X., Weiss, R.G., (2007) Tetrahedron, 63, p. 7375 
504 |a Kawano, S., Fujita, N., Shinkai, S., (2003) Chem. Commun., p. 1352 
504 |a Llusar, M., Sanchez, C., (2008) Chem. Mater., 20, p. 782 
504 |a Sugiyasu, K., Fujita, N., Shinkai, S., (2004) Angew. Chem., Int. Ed., 43, p. 1229 
504 |a Edelsztein, V.C., Burton, G., Di Chenna, P.H., (2010) Tetrahedron, 66, p. 2162 
504 |a Weil, T., Vosch, T., Hofkens, J., Peneva, K., Müllen, K., (2010) Angew. Chem., Int. Ed., 49, p. 2 
504 |a Inokuchi, H., (1988) Angew. Chem., Int. Ed. Engl., 27, p. 1747 
504 |a Li, C., Schöneboom, J., Liu, Z., Pschirer, N.G., Erk, P., Herrmann, A., Müllen, K., (2009) Chem.-Eur. J., 15, p. 878 
504 |a Peneva, K., Mihov, G., Nolde, F., Rocha, S., Hotta, J.-I., Braeckmans, K., Hofkens, J., Müllen, K., (2008) Angew. Chem., Int. Ed., 47, p. 3372 
504 |a Würthner, F., Hanke, B., Lysetska, M., Lambright, G., Harms, G.S., (2005) Org. Lett., 7, p. 967 
504 |a Wu, H., Xue, L., Shi, Y., Chen, Y., Li, X., (2011) Langmuir, 27, pp. 3074-3082 
504 |a Brome, W.R., De Jong, J.J.D., Kudernac, T., Walko, M., Lucus, L.M., Uchida, K., Van Esch, J.H., Feringa, B.L., (2005) Chem.-Eur. J., 11, p. 6414 
504 |a Irie, M., (2000) Chem. Rev., 100, p. 1685 
504 |a Tsivgoulis, G.M., Lehn, J.-M., (1996) Chem.-Eur. J., 1, p. 285 
504 |a Fukaminato, T., Sasaki, T., Kawai, T., Tamai, T., Irie, M., (2004) J. Am. Chem. Soc., 126, p. 14843 
504 |a Giordano, L., Jovin, T.M., Irie, M., Jares-Erijman, E.A., (2002) J. Am. Chem. Soc., 124, p. 7481 
504 |a Matsuda, K., Irie, M., (2004) J. Photochem. Photobiol., C, 5, p. 169 
504 |a Raymo, F.M., Tomasulo, M., (2005) J. Phys. Chem. A, 109, p. 7343 
504 |a Tian, H., Yang, S., (2004) Chem. Soc. Rev., 33, p. 85 
504 |a Kobatake, S., Yamada, M., Yamada, T., Irie, M., (1999) J. Am. Chem. Soc., 121, p. 8450 
504 |a Bae, S.W., Tan, W., Hong, J., (2012) Chem. Commun., 48, p. 2270 
504 |a Chung, J.W., Yoon, S., Lim, S., An, B., Park, S.Y., (2009) Angew. Chem., Int. Ed., 48, p. 7030 
504 |a Schneider, M., Mu, K., (2000) Chem. Mater., 12, p. 352 
520 3 |a The modulation of the fluorescence emission of a perylene dye between ON and OFF states was achieved with high efficiency by means of a diarylethene photochromic compound in an organogel medium. Fluorescent gels were prepared from a steroidal low molecular weight organogelator doped with the perylene fluorophore. The compatibility of the photochromic compound in this medium and the non-destructive readout capability were demonstrated. The dye doped organogel was further used as a template and an innovative method was employed to grow fluorescent silica spherical nanoparticles with physically and chemically admixed perylene dye. © 2012 The Royal Society of Chemistry.  |l eng 
593 |a CIHIDECAR-CONICET, Facultad de Ciencias Exactas y Naturales, Dto. Química Orgánica, 3er piso Pabellón II, Cdad. Universitaria, Buenos Aires, Argentina 
593 |a UMYMFOR(CONICET-UBA), Facultad de Ciencias Exactas y Natura-les, Dto. Química Orgánica, 3er piso Pabe-llón II, Cdad. Universitaria, Buenos Aires, Argentina 
593 |a Max Planck Institute for Polymer Research, Ackermannweg 10, D-55128, Mainz, Germany 
690 1 0 |a DIARYLETHENES 
690 1 0 |a DYE-DOPED 
690 1 0 |a FLUORESCENCE EMISSION 
690 1 0 |a FLUORESCENT NANOPARTICLES 
690 1 0 |a INNOVATIVE METHOD 
690 1 0 |a LOW MOLECULAR WEIGHT 
690 1 0 |a NON DESTRUCTIVE 
690 1 0 |a ORGANO-GELATOR 
690 1 0 |a ORGANOGELS 
690 1 0 |a PERYLENE DYES 
690 1 0 |a PERYLENES 
690 1 0 |a PHOTOCHROMIC COMPOUND 
690 1 0 |a PHOTOSWITCHING 
690 1 0 |a SPHERICAL NANOPARTICLES 
690 1 0 |a TEMPLATED SYNTHESIS 
690 1 0 |a DOPING (ADDITIVES) 
690 1 0 |a NANOPARTICLES 
690 1 0 |a PHOTOCHROMISM 
690 1 0 |a POLYCYCLIC AROMATIC HYDROCARBONS 
690 1 0 |a SILICA 
690 1 0 |a FLUORESCENCE 
700 1 |a Jares-Erijman, E.A. 
700 1 |a Müllen, K. 
700 1 |a Di Chenna, P.H. 
700 1 |a Spagnuolo, C.C. 
773 0 |d 2012  |g v. 22  |h pp. 21857-21861  |k n. 41  |p J. Mater. Chem.  |x 09599428  |w (AR-BaUEN)CENRE-580  |t Journal of Materials Chemistry 
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856 4 0 |u https://hdl.handle.net/20.500.12110/paper_09599428_v22_n41_p21857_Edelsztein  |y Handle 
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