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  • Fonte: Angewandte Chemie. Unidade: IFSC

    Assuntos: FOTOQUÍMICA, BORO, ESPECTROSCOPIA

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    • ABNT

      LENZ, Philipp et al. Oxy-borylenes as photoreductants: synthesis and application in dehalogenation and detosylation reactions. Angewandte Chemie, v. 61, n. 42, p. e202209391-1-e202209391-7, 2022Tradução . . Disponível em: https://doi.org/10.1002/anie.202209391. Acesso em: 21 out. 2025.
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      Lenz, P., Oshimizu, R., Klabunde, S., Daniliuc, C. G., Mück-Lichtenfeld, C., Tendyck, J. C., et al. (2022). Oxy-borylenes as photoreductants: synthesis and application in dehalogenation and detosylation reactions. Angewandte Chemie, 61( 42), e202209391-1-e202209391-7. doi:10.1002/anie.202209391
    • NLM

      Lenz P, Oshimizu R, Klabunde S, Daniliuc CG, Mück-Lichtenfeld C, Tendyck JC, Mori T, Uhl W, Hansen MR, Eckert H, Yamaguchi S, Studer A. Oxy-borylenes as photoreductants: synthesis and application in dehalogenation and detosylation reactions [Internet]. Angewandte Chemie. 2022 ; 61( 42): e202209391-1-e202209391-7.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/anie.202209391
    • Vancouver

      Lenz P, Oshimizu R, Klabunde S, Daniliuc CG, Mück-Lichtenfeld C, Tendyck JC, Mori T, Uhl W, Hansen MR, Eckert H, Yamaguchi S, Studer A. Oxy-borylenes as photoreductants: synthesis and application in dehalogenation and detosylation reactions [Internet]. Angewandte Chemie. 2022 ; 61( 42): e202209391-1-e202209391-7.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/anie.202209391
  • Fonte: Chemical Science. Unidade: IFSC

    Assuntos: DIFRAÇÃO POR RAIOS X, ESPECTROSCOPIA, SAIS

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    • ABNT

      TAO, Xin et al. The special role of B(C6F5)3 in the single electron reduction of quinones by radicals. Chemical Science, v. No 2018, n. 41, p. 8011-8018, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8sc03005g. Acesso em: 21 out. 2025.
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      Tao, X., Daniliuc, C. G., Knitsch, R., Hansen, M. R., Eckert, H., Lübbesmeyer, M., et al. (2018). The special role of B(C6F5)3 in the single electron reduction of quinones by radicals. Chemical Science, No 2018( 41), 8011-8018. doi:10.1039/c8sc03005g
    • NLM

      Tao X, Daniliuc CG, Knitsch R, Hansen MR, Eckert H, Lübbesmeyer M, Studer A, Kehr G, Erker G. The special role of B(C6F5)3 in the single electron reduction of quinones by radicals [Internet]. Chemical Science. 2018 ; No 2018( 41): 8011-8018.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c8sc03005g
    • Vancouver

      Tao X, Daniliuc CG, Knitsch R, Hansen MR, Eckert H, Lübbesmeyer M, Studer A, Kehr G, Erker G. The special role of B(C6F5)3 in the single electron reduction of quinones by radicals [Internet]. Chemical Science. 2018 ; No 2018( 41): 8011-8018.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c8sc03005g
  • Fonte: Program. Nome do evento: Brazilian MRS Meeting. Unidade: IFSC

    Assuntos: RESSONÂNCIA MAGNÉTICA ELETRÔNICA, MATERIAIS, DISPOSITIVOS ÓPTICOS

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    • ABNT

      DOERENKAMP, Carsten et al. Solid-state NMR spectroscopy as tool for investigation of surface modified silica particles. 2018, Anais.. Rio de Janeiro: Sociedade Brasileira de Pesquisa em Materiais - SBPMat, 2018. Disponível em: https://new.eventweb.com.br/xviisbpmat/specific-files/grabFile.php?codigo=4FWJ. Acesso em: 21 out. 2025.
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      Doerenkamp, C., Arai, M. S., Grüner, M., Surmiak, S., Studer, A., de Camargo, A. S. S., & Eckert, H. (2018). Solid-state NMR spectroscopy as tool for investigation of surface modified silica particles. In Program. Rio de Janeiro: Sociedade Brasileira de Pesquisa em Materiais - SBPMat. Recuperado de https://new.eventweb.com.br/xviisbpmat/specific-files/grabFile.php?codigo=4FWJ
    • NLM

      Doerenkamp C, Arai MS, Grüner M, Surmiak S, Studer A, de Camargo ASS, Eckert H. Solid-state NMR spectroscopy as tool for investigation of surface modified silica particles [Internet]. Program. 2018 ;[citado 2025 out. 21 ] Available from: https://new.eventweb.com.br/xviisbpmat/specific-files/grabFile.php?codigo=4FWJ
    • Vancouver

      Doerenkamp C, Arai MS, Grüner M, Surmiak S, Studer A, de Camargo ASS, Eckert H. Solid-state NMR spectroscopy as tool for investigation of surface modified silica particles [Internet]. Program. 2018 ;[citado 2025 out. 21 ] Available from: https://new.eventweb.com.br/xviisbpmat/specific-files/grabFile.php?codigo=4FWJ
  • Fonte: Physical Chemistry Chemical Physics. Unidade: IFSC

    Assuntos: RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, MAGNETISMO

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    • ABNT

      MASSOLLE, Anja et al. Towards reliable references for electron paramagnetic resonance parameters based on quantum chemistry: the case of verdazyl radicals. Physical Chemistry Chemical Physics, v. 20, n. 11, p. 7661-7675, 2018Tradução . . Disponível em: https://doi.org/10.1039/c7cp05657e. Acesso em: 21 out. 2025.
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      Massolle, A., Dresselhaus, T., Eusterwiemann, S., Doerenkamp, C., Eckert, H., Studer, A., & Neugebauer, J. (2018). Towards reliable references for electron paramagnetic resonance parameters based on quantum chemistry: the case of verdazyl radicals. Physical Chemistry Chemical Physics, 20( 11), 7661-7675. doi:10.1039/c7cp05657e
    • NLM

      Massolle A, Dresselhaus T, Eusterwiemann S, Doerenkamp C, Eckert H, Studer A, Neugebauer J. Towards reliable references for electron paramagnetic resonance parameters based on quantum chemistry: the case of verdazyl radicals [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 11): 7661-7675.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c7cp05657e
    • Vancouver

      Massolle A, Dresselhaus T, Eusterwiemann S, Doerenkamp C, Eckert H, Studer A, Neugebauer J. Towards reliable references for electron paramagnetic resonance parameters based on quantum chemistry: the case of verdazyl radicals [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 11): 7661-7675.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c7cp05657e
  • Fonte: Physical Chemistry Chemical Physics. Unidade: IFSC

    Assuntos: RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, MAGNETISMO

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      EXNER, Jessica et al. Antiferromagnetic ordering based on intermolecular London dispersion interactions in amphiphilic TEMPO ammonium salts. Physical Chemistry Chemical Physics, v. 20, n. 46, p. 28979-28983, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8cp05837g. Acesso em: 21 out. 2025.
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      Exner, J., Eusterwiemann, S., Janka, O., Doerenkamp, C., Massolle, A., Niehaus, O., et al. (2018). Antiferromagnetic ordering based on intermolecular London dispersion interactions in amphiphilic TEMPO ammonium salts. Physical Chemistry Chemical Physics, 20( 46), 28979-28983. doi:10.1039/c8cp05837g
    • NLM

      Exner J, Eusterwiemann S, Janka O, Doerenkamp C, Massolle A, Niehaus O, Daniliuc CG, Pöttgen R, Neugebauer J, Studer A, Eckert H. Antiferromagnetic ordering based on intermolecular London dispersion interactions in amphiphilic TEMPO ammonium salts [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 46): 28979-28983.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c8cp05837g
    • Vancouver

      Exner J, Eusterwiemann S, Janka O, Doerenkamp C, Massolle A, Niehaus O, Daniliuc CG, Pöttgen R, Neugebauer J, Studer A, Eckert H. Antiferromagnetic ordering based on intermolecular London dispersion interactions in amphiphilic TEMPO ammonium salts [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 46): 28979-28983.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c8cp05837g
  • Fonte: Physical Chemistry Chemical Physics. Unidade: IFSC

    Assuntos: RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, MAGNETISMO

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    • ABNT

      EUSTERWIEMANN, Steffen et al. Ferro- or antiferromagnetism? Heisenberg chains in the crystal structures of verdazyl radicals. Physical Chemistry Chemical Physics, v. 20, n. 35, p. 22902-22908, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8cp03332c. Acesso em: 21 out. 2025.
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      Eusterwiemann, S., Doerenkamp, C., Dresselhaus, T., Janka, O., Daniliuc, C. G., Pöttgen, R., et al. (2018). Ferro- or antiferromagnetism? Heisenberg chains in the crystal structures of verdazyl radicals. Physical Chemistry Chemical Physics, 20( 35), 22902-22908. doi:10.1039/c8cp03332c
    • NLM

      Eusterwiemann S, Doerenkamp C, Dresselhaus T, Janka O, Daniliuc CG, Pöttgen R, Studer A, Eckert H, Neugebauer J. Ferro- or antiferromagnetism? Heisenberg chains in the crystal structures of verdazyl radicals [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 35): 22902-22908.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c8cp03332c
    • Vancouver

      Eusterwiemann S, Doerenkamp C, Dresselhaus T, Janka O, Daniliuc CG, Pöttgen R, Studer A, Eckert H, Neugebauer J. Ferro- or antiferromagnetism? Heisenberg chains in the crystal structures of verdazyl radicals [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 35): 22902-22908.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c8cp03332c
  • Fonte: Chemistry: a European Journal. Unidade: IFSC

    Assuntos: COMPOSTOS DE COORDENAÇÃO, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, DNA

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      GREULICH, Tobias W. et al. Synthesis and physical properties of strained doubly phosphorus - bridged biaryls and viologens. Chemistry: a European Journal, v. 23, n. 25, p. 6029-6033, 2017Tradução . . Disponível em: https://doi.org/10.1002/chem.201605272. Acesso em: 21 out. 2025.
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      Greulich, T. W., Yamaguchi, E., Doerenkamp, C., Lebbesmeyer, M., Daniliuc, C. G., Fukazawa, A., et al. (2017). Synthesis and physical properties of strained doubly phosphorus - bridged biaryls and viologens. Chemistry: a European Journal, 23( 25), 6029-6033. doi:10.1002/chem.201605272
    • NLM

      Greulich TW, Yamaguchi E, Doerenkamp C, Lebbesmeyer M, Daniliuc CG, Fukazawa A, Eckert H, Yamaguchi S, Studer A. Synthesis and physical properties of strained doubly phosphorus - bridged biaryls and viologens [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6029-6033.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201605272
    • Vancouver

      Greulich TW, Yamaguchi E, Doerenkamp C, Lebbesmeyer M, Daniliuc CG, Fukazawa A, Eckert H, Yamaguchi S, Studer A. Synthesis and physical properties of strained doubly phosphorus - bridged biaryls and viologens [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6029-6033.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201605272
  • Fonte: Chemistry: a European Journal. Unidade: IFSC

    Assuntos: COMPOSTOS DE COORDENAÇÃO, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, MAGNETISMO

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      EUSTERWIEMANN, Steffen et al. Cooperative magnetism in crystalline n-aryl-substituted verdazyl radicals: first-principles predictions and experimental results. Chemistry: a European Journal, v. 23, n. 25, p. 6069-6082, 2017Tradução . . Disponível em: https://doi.org/10.1002/chem.201700988. Acesso em: 21 out. 2025.
    • APA

      Eusterwiemann, S., Dresselhaus, T., Doerenkamp, C., Janka, O., Niehaus, O., Massolle, A., et al. (2017). Cooperative magnetism in crystalline n-aryl-substituted verdazyl radicals: first-principles predictions and experimental results. Chemistry: a European Journal, 23( 25), 6069-6082. doi:10.1002/chem.201700988
    • NLM

      Eusterwiemann S, Dresselhaus T, Doerenkamp C, Janka O, Niehaus O, Massolle A, Daniliuc CG, Eckert H, Pöttgen R, Neugebauer J, Studer A. Cooperative magnetism in crystalline n-aryl-substituted verdazyl radicals: first-principles predictions and experimental results [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6069-6082.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201700988
    • Vancouver

      Eusterwiemann S, Dresselhaus T, Doerenkamp C, Janka O, Niehaus O, Massolle A, Daniliuc CG, Eckert H, Pöttgen R, Neugebauer J, Studer A. Cooperative magnetism in crystalline n-aryl-substituted verdazyl radicals: first-principles predictions and experimental results [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6069-6082.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201700988
  • Fonte: Chemistry: a European Journal. Unidade: IFSC

    Assuntos: RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, NANOPARTÍCULAS, QUÍMICA ORGÂNICA, SILÍCIO

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      SURMIAK, Sabrina K. et al. Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions. Chemistry: a European Journal, v. 23, n. 25, p. 6019-6028, 2017Tradução . . Disponível em: https://doi.org/10.1002/chem.201604508. Acesso em: 21 out. 2025.
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      Surmiak, S. K., Doerenkamp, C., Selter, P., Peterlechner, M., Schäfer, A. H., Eckert, H., & Studer, A. (2017). Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions. Chemistry: a European Journal, 23( 25), 6019-6028. doi:10.1002/chem.201604508
    • NLM

      Surmiak SK, Doerenkamp C, Selter P, Peterlechner M, Schäfer AH, Eckert H, Studer A. Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6019-6028.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201604508
    • Vancouver

      Surmiak SK, Doerenkamp C, Selter P, Peterlechner M, Schäfer AH, Eckert H, Studer A. Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6019-6028.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201604508
  • Fonte: Program Book. Nome do evento: Brazilian MRS Meeting. Unidade: IFSC

    Assuntos: MATERIAIS MAGNÉTICOS, FERROMAGNETISMO

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    • ABNT

      DOERENKAMP, Carsten et al. Controlling cooperative magnetism in organic radical systems: structure/property correlations in crystalline verdazyl radicals. 2017, Anais.. Rio de Janeiro: Sociedade Brasileira de Pesquisa em Materiais - SBPMat, 2017. Disponível em: http://www.eventweb.com.br/xvisbpmat/specific-files/grabFile.php?codigo=BHZE. Acesso em: 21 out. 2025.
    • APA

      Doerenkamp, C., Eusterwiemann, S., Dresselhaus, T., Massolle, A., Janka, O., Oliveira Junior, M. de, et al. (2017). Controlling cooperative magnetism in organic radical systems: structure/property correlations in crystalline verdazyl radicals. In Program Book. Rio de Janeiro: Sociedade Brasileira de Pesquisa em Materiais - SBPMat. Recuperado de http://www.eventweb.com.br/xvisbpmat/specific-files/grabFile.php?codigo=BHZE
    • NLM

      Doerenkamp C, Eusterwiemann S, Dresselhaus T, Massolle A, Janka O, Oliveira Junior M de, Daniliuc CG, Neugebauer J, Pöttgen R, Studer A, Eckert H. Controlling cooperative magnetism in organic radical systems: structure/property correlations in crystalline verdazyl radicals [Internet]. Program Book. 2017 ;[citado 2025 out. 21 ] Available from: http://www.eventweb.com.br/xvisbpmat/specific-files/grabFile.php?codigo=BHZE
    • Vancouver

      Doerenkamp C, Eusterwiemann S, Dresselhaus T, Massolle A, Janka O, Oliveira Junior M de, Daniliuc CG, Neugebauer J, Pöttgen R, Studer A, Eckert H. Controlling cooperative magnetism in organic radical systems: structure/property correlations in crystalline verdazyl radicals [Internet]. Program Book. 2017 ;[citado 2025 out. 21 ] Available from: http://www.eventweb.com.br/xvisbpmat/specific-files/grabFile.php?codigo=BHZE
  • Fonte: Angewandte Chemie International Edition. Unidade: IFSC

    Assuntos: ESPECTROSCOPIA, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, REDUÇÃO

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      TAO, Xin et al. Reduction of dioxygen by radical/B(p-C6F4X)3 pairs to give isolable bis(borane)superoxide compounds. Angewandte Chemie International Edition, v. 56, n. 52, p. 16641-16644, 2017Tradução . . Disponível em: https://doi.org/10.1002/anie.201709309. Acesso em: 21 out. 2025.
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      Tao, X., Daniliuc, C. G., Janka, O., Pöttgen, R., Knitsch, R., Hansen, M. R., et al. (2017). Reduction of dioxygen by radical/B(p-C6F4X)3 pairs to give isolable bis(borane)superoxide compounds. Angewandte Chemie International Edition, 56( 52), 16641-16644. doi:10.1002/anie.201709309
    • NLM

      Tao X, Daniliuc CG, Janka O, Pöttgen R, Knitsch R, Hansen MR, Eckert H, Lübbesmeyer M, Studer A, Kehr G, Erker G. Reduction of dioxygen by radical/B(p-C6F4X)3 pairs to give isolable bis(borane)superoxide compounds [Internet]. Angewandte Chemie International Edition. 2017 ; 56( 52): 16641-16644.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/anie.201709309
    • Vancouver

      Tao X, Daniliuc CG, Janka O, Pöttgen R, Knitsch R, Hansen MR, Eckert H, Lübbesmeyer M, Studer A, Kehr G, Erker G. Reduction of dioxygen by radical/B(p-C6F4X)3 pairs to give isolable bis(borane)superoxide compounds [Internet]. Angewandte Chemie International Edition. 2017 ; 56( 52): 16641-16644.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/anie.201709309
  • Fonte: Chemistry: a European Journal. Unidade: IFSC

    Assuntos: COMPOSTOS DE COORDENAÇÃO, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, DNA

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      ELMER, Lisa-Maria et al. The chemistry of a non-interacting vicinal frustrated phosphane/ borane lewis pair. Chemistry: a European Journal, v. 23, n. 25, p. 6056-6068, 2017Tradução . . Disponível em: https://doi.org/10.1002/chem.201603954. Acesso em: 21 out. 2025.
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      Elmer, L. -M., Kehr, G., Daniliuc, C. G., Siedow, M., Eckert, H., Tesch, M., et al. (2017). The chemistry of a non-interacting vicinal frustrated phosphane/ borane lewis pair. Chemistry: a European Journal, 23( 25), 6056-6068. doi:10.1002/chem.201603954
    • NLM

      Elmer L-M, Kehr G, Daniliuc CG, Siedow M, Eckert H, Tesch M, Studer A, Williams K, Warren TH, Erker G. The chemistry of a non-interacting vicinal frustrated phosphane/ borane lewis pair [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6056-6068.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201603954
    • Vancouver

      Elmer L-M, Kehr G, Daniliuc CG, Siedow M, Eckert H, Tesch M, Studer A, Williams K, Warren TH, Erker G. The chemistry of a non-interacting vicinal frustrated phosphane/ borane lewis pair [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6056-6068.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201603954
  • Fonte: Journal of Solid State Chemistry. Unidade: IFSC

    Assuntos: ESPECTROSCOPIA, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      VRIES, Wilke de et al. Synthesis and characterization of amorphous mesoporous silica using TEMPO-functionalized amphiphilic templates. Journal of Solid State Chemistry, v. 237, p. 93-98, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.jssc.2016.01.023. Acesso em: 21 out. 2025.
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      Vries, W. de, Doerenkamp, C., Zeng, Z., Oliveira Junior, M. de, Niehaus, O., Pöttgen, R., et al. (2016). Synthesis and characterization of amorphous mesoporous silica using TEMPO-functionalized amphiphilic templates. Journal of Solid State Chemistry, 237, 93-98. doi:10.1016/j.jssc.2016.01.023
    • NLM

      Vries W de, Doerenkamp C, Zeng Z, Oliveira Junior M de, Niehaus O, Pöttgen R, Studer A, Eckert H. Synthesis and characterization of amorphous mesoporous silica using TEMPO-functionalized amphiphilic templates [Internet]. Journal of Solid State Chemistry. 2016 ; 237 93-98.[citado 2025 out. 21 ] Available from: https://doi.org/10.1016/j.jssc.2016.01.023
    • Vancouver

      Vries W de, Doerenkamp C, Zeng Z, Oliveira Junior M de, Niehaus O, Pöttgen R, Studer A, Eckert H. Synthesis and characterization of amorphous mesoporous silica using TEMPO-functionalized amphiphilic templates [Internet]. Journal of Solid State Chemistry. 2016 ; 237 93-98.[citado 2025 out. 21 ] Available from: https://doi.org/10.1016/j.jssc.2016.01.023
  • Fonte: Chimia. Unidade: IFSC

    Assuntos: SPIN, FLUORESCÊNCIA

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      EUSTERWIEMANN, Steffen et al. Effect of the C(3)-substituent in verdazyl radicals on their profluorescent behavior. Chimia, v. 70, n. 3, p. 172-176, 2016Tradução . . Disponível em: https://doi.org/10.2533/chimia.2016.172. Acesso em: 21 out. 2025.
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      Eusterwiemann, S., Matuschek, D., Stegemann, L., Klabunde, S., Doerenkamp, C. C., Daniliuc, C. G., et al. (2016). Effect of the C(3)-substituent in verdazyl radicals on their profluorescent behavior. Chimia, 70( 3), 172-176. doi:10.2533/chimia.2016.172
    • NLM

      Eusterwiemann S, Matuschek D, Stegemann L, Klabunde S, Doerenkamp CC, Daniliuc CG, Doltsinis NL, Strassert CA, Eckert H, Studer A. Effect of the C(3)-substituent in verdazyl radicals on their profluorescent behavior [Internet]. Chimia. 2016 ; 70( 3): 172-176.[citado 2025 out. 21 ] Available from: https://doi.org/10.2533/chimia.2016.172
    • Vancouver

      Eusterwiemann S, Matuschek D, Stegemann L, Klabunde S, Doerenkamp CC, Daniliuc CG, Doltsinis NL, Strassert CA, Eckert H, Studer A. Effect of the C(3)-substituent in verdazyl radicals on their profluorescent behavior [Internet]. Chimia. 2016 ; 70( 3): 172-176.[citado 2025 out. 21 ] Available from: https://doi.org/10.2533/chimia.2016.172
  • Fonte: Chemical Science. Unidade: IFSC

    Assuntos: FLUORESCÊNCIA, ESPECTROSCOPIA

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      MATUSCHEK, David et al. Profluorescent verdazyl radicals: synthesis and characterization. Chemical Science, v. 6, n. 8, p. 4712-4716, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5sc00724k. Acesso em: 21 out. 2025.
    • APA

      Matuschek, D., Eusterwiemann, S., Stegemann, L., Doerenkamp, C., Wibbeling, B., Daniliuc, C. G., et al. (2015). Profluorescent verdazyl radicals: synthesis and characterization. Chemical Science, 6( 8), 4712-4716. doi:10.1039/c5sc00724k
    • NLM

      Matuschek D, Eusterwiemann S, Stegemann L, Doerenkamp C, Wibbeling B, Daniliuc CG, Doltsinis NL, Strassert CA, Eckert H, Studer A. Profluorescent verdazyl radicals: synthesis and characterization [Internet]. Chemical Science. 2015 ; 6( 8): 4712-4716.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c5sc00724k
    • Vancouver

      Matuschek D, Eusterwiemann S, Stegemann L, Doerenkamp C, Wibbeling B, Daniliuc CG, Doltsinis NL, Strassert CA, Eckert H, Studer A. Profluorescent verdazyl radicals: synthesis and characterization [Internet]. Chemical Science. 2015 ; 6( 8): 4712-4716.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c5sc00724k
  • Fonte: Chemical Communications. Unidade: IFSC

    Assuntos: NANOPARTÍCULAS, SILÍCIO, QUÍMICA ORGÂNICA

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    • ABNT

      DICKSCHAT, Arne T. et al. Bifunctional mesoporous silica nanoparticles as cooperative catalysts for the Tsuji-Trost reaction: tuning the reactivity of silica nanoparticles. Chemical Communications, v. 49, n. 22, p. 2195-2197, 2013Tradução . . Disponível em: https://doi.org/10.1039/c3cc00235g. Acesso em: 21 out. 2025.
    • APA

      Dickschat, A. T., Behrends, F., Surmiak, S., Weiß, M., Eckert, H., & Studer, A. (2013). Bifunctional mesoporous silica nanoparticles as cooperative catalysts for the Tsuji-Trost reaction: tuning the reactivity of silica nanoparticles. Chemical Communications, 49( 22), 2195-2197. doi:10.1039/c3cc00235g
    • NLM

      Dickschat AT, Behrends F, Surmiak S, Weiß M, Eckert H, Studer A. Bifunctional mesoporous silica nanoparticles as cooperative catalysts for the Tsuji-Trost reaction: tuning the reactivity of silica nanoparticles [Internet]. Chemical Communications. 2013 ; 49( 22): 2195-2197.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c3cc00235g
    • Vancouver

      Dickschat AT, Behrends F, Surmiak S, Weiß M, Eckert H, Studer A. Bifunctional mesoporous silica nanoparticles as cooperative catalysts for the Tsuji-Trost reaction: tuning the reactivity of silica nanoparticles [Internet]. Chemical Communications. 2013 ; 49( 22): 2195-2197.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c3cc00235g
  • Fonte: Dalton Transactions. Unidade: IFSC

    Assuntos: MATERIAIS (PROPRIEDADES FÍSICO-QUÍMICAS), ARGILAS

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      ZENG, Zhaoyang et al. Synthesis and characterization of inorganic-organic hybrid materials based on the intercalation of stable organic radicals into a fluoromica clay. Dalton Transactions, v. 42, n. 24, p. 8585-8596, 2013Tradução . . Disponível em: https://doi.org/10.1039/c3dt50627d. Acesso em: 21 out. 2025.
    • APA

      Zeng, Z., Matuschek, D., Studer, A., Schwickert, C., Pöttgenc, R., & Eckert, H. (2013). Synthesis and characterization of inorganic-organic hybrid materials based on the intercalation of stable organic radicals into a fluoromica clay. Dalton Transactions, 42( 24), 8585-8596. doi:10.1039/c3dt50627d
    • NLM

      Zeng Z, Matuschek D, Studer A, Schwickert C, Pöttgenc R, Eckert H. Synthesis and characterization of inorganic-organic hybrid materials based on the intercalation of stable organic radicals into a fluoromica clay [Internet]. Dalton Transactions. 2013 ; 42( 24): 8585-8596.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c3dt50627d
    • Vancouver

      Zeng Z, Matuschek D, Studer A, Schwickert C, Pöttgenc R, Eckert H. Synthesis and characterization of inorganic-organic hybrid materials based on the intercalation of stable organic radicals into a fluoromica clay [Internet]. Dalton Transactions. 2013 ; 42( 24): 8585-8596.[citado 2025 out. 21 ] Available from: https://doi.org/10.1039/c3dt50627d
  • Fonte: Macromolecules. Unidade: IFSC

    Assuntos: RESSONÂNCIA MAGNÉTICA, POLIMERIZAÇÃO

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      BEHRENDS, Frederik et al. Polynitroxides from alkoxyamine monomers: structural and kinetic investigations by solid state NMR. Macromolecules, v. 46, n. 7, p. 2553-2561, 2013Tradução . . Disponível em: https://doi.org/10.1021/ma400351q. Acesso em: 21 out. 2025.
    • APA

      Behrends, F., Wagner, H., Studer, A., Niehaus, O., Pöttgen, R., & Eckert, H. (2013). Polynitroxides from alkoxyamine monomers: structural and kinetic investigations by solid state NMR. Macromolecules, 46( 7), 2553-2561. doi:10.1021/ma400351q
    • NLM

      Behrends F, Wagner H, Studer A, Niehaus O, Pöttgen R, Eckert H. Polynitroxides from alkoxyamine monomers: structural and kinetic investigations by solid state NMR [Internet]. Macromolecules. 2013 ; 46( 7): 2553-2561.[citado 2025 out. 21 ] Available from: https://doi.org/10.1021/ma400351q
    • Vancouver

      Behrends F, Wagner H, Studer A, Niehaus O, Pöttgen R, Eckert H. Polynitroxides from alkoxyamine monomers: structural and kinetic investigations by solid state NMR [Internet]. Macromolecules. 2013 ; 46( 7): 2553-2561.[citado 2025 out. 21 ] Available from: https://doi.org/10.1021/ma400351q
  • Fonte: Chemistry - A European Journal. Unidade: IFSC

    Assuntos: ÁCIDOS, ESPECTROSCOPIA DE RESSONÂNCIA MAGNÉTICA NUCLEAR, CATÁLISE

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    • ABNT

      DICKSCHAT, Arne T. et al. Preparation of bifunctional mesoporous silica nanoparticles by orthogonal click reactions and their application in cooperative catalysis. Chemistry - A European Journal, v. 18, n. 52, p. 16689-16697, 2012Tradução . . Disponível em: https://doi.org/10.1002/chem.201200499. Acesso em: 21 out. 2025.
    • APA

      Dickschat, A. T., Behrends, F., Bühner, M., Ren, J., Weiß, M., Eckert, H., & Studer, A. (2012). Preparation of bifunctional mesoporous silica nanoparticles by orthogonal click reactions and their application in cooperative catalysis. Chemistry - A European Journal, 18( 52), 16689-16697. doi:10.1002/chem.201200499
    • NLM

      Dickschat AT, Behrends F, Bühner M, Ren J, Weiß M, Eckert H, Studer A. Preparation of bifunctional mesoporous silica nanoparticles by orthogonal click reactions and their application in cooperative catalysis [Internet]. Chemistry - A European Journal. 2012 ; 18( 52): 16689-16697.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201200499
    • Vancouver

      Dickschat AT, Behrends F, Bühner M, Ren J, Weiß M, Eckert H, Studer A. Preparation of bifunctional mesoporous silica nanoparticles by orthogonal click reactions and their application in cooperative catalysis [Internet]. Chemistry - A European Journal. 2012 ; 18( 52): 16689-16697.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/chem.201200499

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