Filtros : "Studer, Armido" Removido: "Doerenkamp, Carsten" Limpar

Filtros



Limitar por data


  • Fonte: Angewandte Chemie. Unidade: IFSC

    Assuntos: FOTOQUÍMICA, BORO, ESPECTROSCOPIA

    Versão PublicadaAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 23 out. 2025.
    • APA

      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. 23 ] 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. 23 ] Available from: https://doi.org/10.1002/anie.202209391
  • Fonte: Physical Chemistry Chemical Physics. Unidade: IFSC

    Assuntos: QUÍMICA QUÂNTICA, LUMINESCÊNCIA, FLUORESCÊNCIA

    PrivadoAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      EXNER, Jessica et al. Electronic effects in profluorescent benzotriazinyl radicals: a combined experimental and theoretical study. Physical Chemistry Chemical Physics, v. 23, n. Ja 2021, p. 2999-3007 + supplementary information, 2021Tradução . . Disponível em: https://doi.org/10.1039/d0cp05732k. Acesso em: 23 out. 2025.
    • APA

      Exner, J., Maisuls, I., Massolle, A., Klabunde, S., Hansen, M. R., Strassert, C. A., et al. (2021). Electronic effects in profluorescent benzotriazinyl radicals: a combined experimental and theoretical study. Physical Chemistry Chemical Physics, 23( Ja 2021), 2999-3007 + supplementary information. doi:10.1039/d0cp05732k
    • NLM

      Exner J, Maisuls I, Massolle A, Klabunde S, Hansen MR, Strassert CA, Neugebauer J, Eckert H, Studer A. Electronic effects in profluorescent benzotriazinyl radicals: a combined experimental and theoretical study [Internet]. Physical Chemistry Chemical Physics. 2021 ; 23( Ja 2021): 2999-3007 + supplementary information.[citado 2025 out. 23 ] Available from: https://doi.org/10.1039/d0cp05732k
    • Vancouver

      Exner J, Maisuls I, Massolle A, Klabunde S, Hansen MR, Strassert CA, Neugebauer J, Eckert H, Studer A. Electronic effects in profluorescent benzotriazinyl radicals: a combined experimental and theoretical study [Internet]. Physical Chemistry Chemical Physics. 2021 ; 23( Ja 2021): 2999-3007 + supplementary information.[citado 2025 out. 23 ] Available from: https://doi.org/10.1039/d0cp05732k
  • Fonte: Chemical Science. Unidade: IFSC

    Assuntos: DIFRAÇÃO POR RAIOS X, ESPECTROSCOPIA, SAIS

    Versão PublicadaAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 23 out. 2025.
    • APA

      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. 23 ] 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. 23 ] Available from: https://doi.org/10.1039/c8sc03005g
  • Fonte: Angewandte Chemie International Edition. Unidade: IFSC

    Assuntos: ESPECTROSCOPIA, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, REDUÇÃO

    PrivadoAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 23 out. 2025.
    • APA

      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. 23 ] 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. 23 ] Available from: https://doi.org/10.1002/anie.201709309
  • Fonte: Chemistry: a European Journal. Unidade: IFSC

    Assuntos: COMPOSTOS DE COORDENAÇÃO, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, DNA

    PrivadoAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 23 out. 2025.
    • APA

      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. 23 ] 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. 23 ] Available from: https://doi.org/10.1002/chem.201603954
  • Fonte: Chimia. Unidade: IFSC

    Assuntos: SPIN, FLUORESCÊNCIA

    PrivadoAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 23 out. 2025.
    • APA

      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. 23 ] 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. 23 ] Available from: https://doi.org/10.2533/chimia.2016.172
  • Fonte: Chemical Communications. Unidade: IFSC

    Assuntos: NANOPARTÍCULAS, SILÍCIO, QUÍMICA ORGÂNICA

    PrivadoAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 23 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. 23 ] 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. 23 ] Available from: https://doi.org/10.1039/c3cc00235g
  • Fonte: Dalton Transactions. Unidade: IFSC

    Assuntos: MATERIAIS (PROPRIEDADES FÍSICO-QUÍMICAS), ARGILAS

    PrivadoAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 23 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. 23 ] 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. 23 ] Available from: https://doi.org/10.1039/c3dt50627d
  • Fonte: Macromolecules. Unidade: IFSC

    Assuntos: RESSONÂNCIA MAGNÉTICA, POLIMERIZAÇÃO

    PrivadoAcesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 23 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. 23 ] 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. 23 ] Available from: https://doi.org/10.1021/ma400351q
  • Fonte: Chemistry - A European Journal. Unidade: IFSC

    Assuntos: ÁCIDOS, ESPECTROSCOPIA DE RESSONÂNCIA MAGNÉTICA NUCLEAR, CATÁLISE

    Acesso à fonteDOIComo citar
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 23 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. 23 ] 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. 23 ] Available from: https://doi.org/10.1002/chem.201200499

Biblioteca Digital de Produção Intelectual da Universidade de São Paulo     2012 - 2025