Filtros : "Cambridge" "GEHLEN, MARCELO HENRIQUE" Removido: "Academic Press" Limpar

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  • Fonte: Photochemical & Photobiological Sciences. Unidades: IQSC, IQ

    Assunto: FOTOQUÍMICA

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    • ABNT

      SILVA, Gustavo Thalmer de Medeiros et al. Highly fluorescent hybrid pigments from anthocyanin- and red wine pyranoanthocyanin-analogs adsorbed on sepiolite clay. Photochemical & Photobiological Sciences, v. 18, p. 1750-1760, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9pp00141g. Acesso em: 15 maio 2024.
    • APA

      Silva, G. T. de M., Silva, K. M. da, Silva, C. P. da, Rodrigues, A. C. B., Oake, J., Gehlen, M. H., et al. (2019). Highly fluorescent hybrid pigments from anthocyanin- and red wine pyranoanthocyanin-analogs adsorbed on sepiolite clay. Photochemical & Photobiological Sciences, 18, 1750-1760. doi:10.1039/c9pp00141g
    • NLM

      Silva GT de M, Silva KM da, Silva CP da, Rodrigues ACB, Oake J, Gehlen MH, Bohne C, Quina FH. Highly fluorescent hybrid pigments from anthocyanin- and red wine pyranoanthocyanin-analogs adsorbed on sepiolite clay [Internet]. Photochemical & Photobiological Sciences. 2019 ; 18 1750-1760.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c9pp00141g
    • Vancouver

      Silva GT de M, Silva KM da, Silva CP da, Rodrigues ACB, Oake J, Gehlen MH, Bohne C, Quina FH. Highly fluorescent hybrid pigments from anthocyanin- and red wine pyranoanthocyanin-analogs adsorbed on sepiolite clay [Internet]. Photochemical & Photobiological Sciences. 2019 ; 18 1750-1760.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c9pp00141g
  • Fonte: Physical Chemistry Chemical Physics. Unidade: IQSC

    Assuntos: FLUORESCÊNCIA, SILÍCIO

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      LINO, Aline Monteiro e GEHLEN, Marcelo Henrique. Styryl dye formation promoted by catalytic centers of piperazine bound to a silica surface traced by single molecule fluorescence microscopy. Physical Chemistry Chemical Physics, v. 19, p. 20984-20990, 2017Tradução . . Disponível em: https://doi.org/10.1039/C7CP03437G. Acesso em: 15 maio 2024.
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      Lino, A. M., & Gehlen, M. H. (2017). Styryl dye formation promoted by catalytic centers of piperazine bound to a silica surface traced by single molecule fluorescence microscopy. Physical Chemistry Chemical Physics, 19, 20984-20990. doi:10.1039/C7CP03437G
    • NLM

      Lino AM, Gehlen MH. Styryl dye formation promoted by catalytic centers of piperazine bound to a silica surface traced by single molecule fluorescence microscopy [Internet]. Physical Chemistry Chemical Physics. 2017 ; 19 20984-20990.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/C7CP03437G
    • Vancouver

      Lino AM, Gehlen MH. Styryl dye formation promoted by catalytic centers of piperazine bound to a silica surface traced by single molecule fluorescence microscopy [Internet]. Physical Chemistry Chemical Physics. 2017 ; 19 20984-20990.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/C7CP03437G
  • Fonte: Chemical Science. Unidade: IQSC

    Assunto: DNA

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      LAUER, Milena Helmer et al. Methyltransferase-directed covalent coupling of fluorophores to DNA. Chemical Science, v. 8, n. 5, p. 3804-3811, 2017Tradução . . Disponível em: https://doi.org/10.1039/c6sc04229e. Acesso em: 15 maio 2024.
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      Lauer, M. H., Vranken, C., Deen, J., Frederickx, W., Vanderline, F. A., Wand, N., et al. (2017). Methyltransferase-directed covalent coupling of fluorophores to DNA. Chemical Science, 8( 5), 3804-3811. doi:10.1039/c6sc04229e
    • NLM

      Lauer MH, Vranken C, Deen J, Frederickx W, Vanderline FA, Wand N, Leen V, Gehlen MH, Hofkens J, Neely RK. Methyltransferase-directed covalent coupling of fluorophores to DNA [Internet]. Chemical Science. 2017 ; 8( 5): 3804-3811.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c6sc04229e
    • Vancouver

      Lauer MH, Vranken C, Deen J, Frederickx W, Vanderline FA, Wand N, Leen V, Gehlen MH, Hofkens J, Neely RK. Methyltransferase-directed covalent coupling of fluorophores to DNA [Internet]. Chemical Science. 2017 ; 8( 5): 3804-3811.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c6sc04229e
  • Fonte: Photochemical & Photobiological Sciences. Unidade: IQSC

    Assunto: FLUORESCÊNCIA

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      LENCIONE, Diego et al. The spatial distribution of the photostability of thionine in zeolite L nanochannels investigated by photobleaching lifetime imaging microscopy. Photochemical & Photobiological Sciences, v. 15, p. 398-404, 2016Tradução . . Disponível em: https://doi.org/10.1039/c5pp00418g. Acesso em: 15 maio 2024.
    • APA

      Lencione, D., Gehlen, M. H., Trujillo, L. N., Leitão, R. C. F., & Albuquerque, R. Q. de. (2016). The spatial distribution of the photostability of thionine in zeolite L nanochannels investigated by photobleaching lifetime imaging microscopy. Photochemical & Photobiological Sciences, 15, 398-404. doi:10.1039/c5pp00418g
    • NLM

      Lencione D, Gehlen MH, Trujillo LN, Leitão RCF, Albuquerque RQ de. The spatial distribution of the photostability of thionine in zeolite L nanochannels investigated by photobleaching lifetime imaging microscopy [Internet]. Photochemical & Photobiological Sciences. 2016 ; 15 398-404.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c5pp00418g
    • Vancouver

      Lencione D, Gehlen MH, Trujillo LN, Leitão RCF, Albuquerque RQ de. The spatial distribution of the photostability of thionine in zeolite L nanochannels investigated by photobleaching lifetime imaging microscopy [Internet]. Photochemical & Photobiological Sciences. 2016 ; 15 398-404.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c5pp00418g
  • Fonte: Photochemical & Photobiological Sciences. Unidade: IQSC

    Assunto: FLUORESCÊNCIA

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    • ABNT

      LAUER, Milena Helmer et al. Fluorescence from bisaryl-substituted maleimide derivatives. Photochemical & Photobiological Sciences, v. 13, n. 6, p. 859-866, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4pp00001c. Acesso em: 15 maio 2024.
    • APA

      Lauer, M. H., Drekener, R. L., Duarte Correia, C. R., & Gehlen, M. H. (2014). Fluorescence from bisaryl-substituted maleimide derivatives. Photochemical & Photobiological Sciences, 13( 6), 859-866. doi:10.1039/c4pp00001c
    • NLM

      Lauer MH, Drekener RL, Duarte Correia CR, Gehlen MH. Fluorescence from bisaryl-substituted maleimide derivatives [Internet]. Photochemical & Photobiological Sciences. 2014 ; 13( 6): 859-866.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c4pp00001c
    • Vancouver

      Lauer MH, Drekener RL, Duarte Correia CR, Gehlen MH. Fluorescence from bisaryl-substituted maleimide derivatives [Internet]. Photochemical & Photobiological Sciences. 2014 ; 13( 6): 859-866.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/c4pp00001c
  • Fonte: Photochemical & Photobiological Sciences. Unidades: IQSC, FFCLRP

    Assuntos: FOTOQUÍMICA, FOTOBIOLOGIA

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      MACHADO, Antonio Eduardo da Hora et al. Solvent effects on the photophysics of 3-(benzoxazol-2-yl)-7(N,N-diethylamino)chromen-2-one. Photochemical & Photobiological Sciences, v. 3, n. 1, p. 79-84, 2004Tradução . . Disponível em: https://doi.org/10.1039/b308121d. Acesso em: 15 maio 2024.
    • APA

      Machado, A. E. da H., Severino, D., Ribeiro, J., De Paula, R., Gehlen, M. H., Oliveira, H. P. M. de, et al. (2004). Solvent effects on the photophysics of 3-(benzoxazol-2-yl)-7(N,N-diethylamino)chromen-2-one. Photochemical & Photobiological Sciences, 3( 1), 79-84. doi:10.1039/b308121d
    • NLM

      Machado AE da H, Severino D, Ribeiro J, De Paula R, Gehlen MH, Oliveira HPM de, Matos M dos S, Miranda JA de. Solvent effects on the photophysics of 3-(benzoxazol-2-yl)-7(N,N-diethylamino)chromen-2-one [Internet]. Photochemical & Photobiological Sciences. 2004 ; 3( 1): 79-84.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/b308121d
    • Vancouver

      Machado AE da H, Severino D, Ribeiro J, De Paula R, Gehlen MH, Oliveira HPM de, Matos M dos S, Miranda JA de. Solvent effects on the photophysics of 3-(benzoxazol-2-yl)-7(N,N-diethylamino)chromen-2-one [Internet]. Photochemical & Photobiological Sciences. 2004 ; 3( 1): 79-84.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/b308121d
  • Fonte: Photochemical and Photobiological Sciences. Unidade: IQSC

    Assuntos: FOTOQUÍMICA, FOTOBIOLOGIA

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      MACHULEK JUNIOR, Amilcar e OLIVEIRA, Hueder Paulo Moisés de e GEHLEN, Marcelo Henrique. Preparation of silver nanoprisms using poly(N-vinyl-2-pyrrolidone) as a colloid-stabilizing agent and the effect of silver nanoparticles on the photophysical properties of cationic dyes. Photochemical and Photobiological Sciences, v. 2, p. 921-925, 2003Tradução . . Disponível em: https://doi.org/10.1039/b302943c. Acesso em: 15 maio 2024.
    • APA

      Machulek Junior, A., Oliveira, H. P. M. de, & Gehlen, M. H. (2003). Preparation of silver nanoprisms using poly(N-vinyl-2-pyrrolidone) as a colloid-stabilizing agent and the effect of silver nanoparticles on the photophysical properties of cationic dyes. Photochemical and Photobiological Sciences, 2, 921-925. doi:10.1039/b302943c
    • NLM

      Machulek Junior A, Oliveira HPM de, Gehlen MH. Preparation of silver nanoprisms using poly(N-vinyl-2-pyrrolidone) as a colloid-stabilizing agent and the effect of silver nanoparticles on the photophysical properties of cationic dyes [Internet]. Photochemical and Photobiological Sciences. 2003 ; 2 921-925.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/b302943c
    • Vancouver

      Machulek Junior A, Oliveira HPM de, Gehlen MH. Preparation of silver nanoprisms using poly(N-vinyl-2-pyrrolidone) as a colloid-stabilizing agent and the effect of silver nanoparticles on the photophysical properties of cationic dyes [Internet]. Photochemical and Photobiological Sciences. 2003 ; 2 921-925.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/b302943c
  • Fonte: Journal of the Chemical Society. Faraday Transactions. Unidade: IQSC

    Assunto: FÍSICO-QUÍMICA ORGÂNICA

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      BUCHVISER, S F e GEHLEN, Marcelo Henrique. Quenching kinetics of the acridine excited state by vinyl monomers in homogeneous and micellar solution. Journal of the Chemical Society. Faraday Transactions, v. 93, n. 6 , p. 1133-9, 1997Tradução . . Disponível em: https://doi.org/10.1039/a605032h. Acesso em: 15 maio 2024.
    • APA

      Buchviser, S. F., & Gehlen, M. H. (1997). Quenching kinetics of the acridine excited state by vinyl monomers in homogeneous and micellar solution. Journal of the Chemical Society. Faraday Transactions, 93( 6 ), 1133-9. doi:10.1039/a605032h
    • NLM

      Buchviser SF, Gehlen MH. Quenching kinetics of the acridine excited state by vinyl monomers in homogeneous and micellar solution [Internet]. Journal of the Chemical Society. Faraday Transactions. 1997 ;93( 6 ): 1133-9.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/a605032h
    • Vancouver

      Buchviser SF, Gehlen MH. Quenching kinetics of the acridine excited state by vinyl monomers in homogeneous and micellar solution [Internet]. Journal of the Chemical Society. Faraday Transactions. 1997 ;93( 6 ): 1133-9.[citado 2024 maio 15 ] Available from: https://doi.org/10.1039/a605032h

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