Filtros : "Philippot, Karine" Limpar

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  • Source: Applied Catalysis A, General. Unidade: IQ

    Subjects: RÓDIO, NANOPARTÍCULAS

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    • ABNT

      GARCIA, Marco Aurélio Suller et al. Study of the influence of 'PPh IND. 3' used as capping ligand or as reaction modifier for hydroformylation reaction involving Rh NPs as precatalyst. Applied Catalysis A, General, v. 548, p. 136-142, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.apcata.2017.08.009. Acesso em: 01 maio 2024.
    • APA

      Garcia, M. A. S., Ibrahim, M., Costa, J. C. S., Corio, P., Gusevskaya, E. V., Santos, E. N. dos, et al. (2017). Study of the influence of 'PPh IND. 3' used as capping ligand or as reaction modifier for hydroformylation reaction involving Rh NPs as precatalyst. Applied Catalysis A, General, 548, 136-142. doi:10.1016/j.apcata.2017.08.009
    • NLM

      Garcia MAS, Ibrahim M, Costa JCS, Corio P, Gusevskaya EV, Santos EN dos, Philippot K, Rossi LM. Study of the influence of 'PPh IND. 3' used as capping ligand or as reaction modifier for hydroformylation reaction involving Rh NPs as precatalyst [Internet]. Applied Catalysis A, General. 2017 ; 548 136-142.[citado 2024 maio 01 ] Available from: https://doi.org/10.1016/j.apcata.2017.08.009
    • Vancouver

      Garcia MAS, Ibrahim M, Costa JCS, Corio P, Gusevskaya EV, Santos EN dos, Philippot K, Rossi LM. Study of the influence of 'PPh IND. 3' used as capping ligand or as reaction modifier for hydroformylation reaction involving Rh NPs as precatalyst [Internet]. Applied Catalysis A, General. 2017 ; 548 136-142.[citado 2024 maio 01 ] Available from: https://doi.org/10.1016/j.apcata.2017.08.009
  • Source: Dalton Transactions. Unidade: IQ

    Subjects: NANOPARTÍCULAS, COMPOSTOS ORGANOMETÁLICOS

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    • ABNT

      COSTA, Natália de Jesus da Silva et al. One-pot organometallic synthesis of alumina-embedded Pd nanoparticles. Dalton Transactions, v. 46, p. 14318-14324, 2017Tradução . . Disponível em: https://doi.org/10.1039/C7DT02792C. Acesso em: 01 maio 2024.
    • APA

      Costa, N. de J. da S., Vono, L. L. R., Wojcieszak, R., Teixeira Neto, É., Philippot, K., & Rossi, L. M. (2017). One-pot organometallic synthesis of alumina-embedded Pd nanoparticles. Dalton Transactions, 46, 14318-14324. doi:10.1039/C7DT02792C
    • NLM

      Costa N de J da S, Vono LLR, Wojcieszak R, Teixeira Neto É, Philippot K, Rossi LM. One-pot organometallic synthesis of alumina-embedded Pd nanoparticles [Internet]. Dalton Transactions. 2017 ; 46 14318-14324.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/C7DT02792C
    • Vancouver

      Costa N de J da S, Vono LLR, Wojcieszak R, Teixeira Neto É, Philippot K, Rossi LM. One-pot organometallic synthesis of alumina-embedded Pd nanoparticles [Internet]. Dalton Transactions. 2017 ; 46 14318-14324.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/C7DT02792C
  • Source: Abstract Book. Conference titles: International Conference on Coordination Chemistry (ICCC). Unidade: IQ

    Assunto: QUÍMICA DE COORDENAÇÃO

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    • ABNT

      COSTA, Natália de Jesus da Silva et al. Synthesis of well-controled nanocatalysts using coordination chemistry concepts. 2016, Anais.. Brest: Instituto de Química, Universidade de São Paulo, 2016. . Acesso em: 01 maio 2024.
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      Costa, N. de J. da S., Guerrero, M., Ibrahim, M., Garcia, M. A. S., Vono, L. L. R., Rossi, L. M., & Philippot, K. (2016). Synthesis of well-controled nanocatalysts using coordination chemistry concepts. In Abstract Book. Brest: Instituto de Química, Universidade de São Paulo.
    • NLM

      Costa N de J da S, Guerrero M, Ibrahim M, Garcia MAS, Vono LLR, Rossi LM, Philippot K. Synthesis of well-controled nanocatalysts using coordination chemistry concepts. Abstract Book. 2016 ;[citado 2024 maio 01 ]
    • Vancouver

      Costa N de J da S, Guerrero M, Ibrahim M, Garcia MAS, Vono LLR, Rossi LM, Philippot K. Synthesis of well-controled nanocatalysts using coordination chemistry concepts. Abstract Book. 2016 ;[citado 2024 maio 01 ]
  • Source: RSC Advances. Unidade: IQ

    Subjects: CATÁLISE, NANOPARTÍCULAS

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      UNGARO, Vitor A et al. A green route for the synthesis of a bitter-taste dipeptide combining biocatalysis, heterogeneous metal catalysis and magnetic nanoparticles. RSC Advances, v. 5, n. 46, p. 36449-36455, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ra02641e. Acesso em: 01 maio 2024.
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      Ungaro, V. A., Liria, C. W., Romagna, C. D., Costa, N. J. S., Philippot, K., Rossi, L. M., & Machini, M. T. (2015). A green route for the synthesis of a bitter-taste dipeptide combining biocatalysis, heterogeneous metal catalysis and magnetic nanoparticles. RSC Advances, 5( 46), 36449-36455. doi:10.1039/c5ra02641e
    • NLM

      Ungaro VA, Liria CW, Romagna CD, Costa NJS, Philippot K, Rossi LM, Machini MT. A green route for the synthesis of a bitter-taste dipeptide combining biocatalysis, heterogeneous metal catalysis and magnetic nanoparticles [Internet]. RSC Advances. 2015 ; 5( 46): 36449-36455.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/c5ra02641e
    • Vancouver

      Ungaro VA, Liria CW, Romagna CD, Costa NJS, Philippot K, Rossi LM, Machini MT. A green route for the synthesis of a bitter-taste dipeptide combining biocatalysis, heterogeneous metal catalysis and magnetic nanoparticles [Internet]. RSC Advances. 2015 ; 5( 46): 36449-36455.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/c5ra02641e
  • Source: ACS Catalysis. Unidade: IQ

    Subjects: NANOPARTÍCULAS, NÍQUEL, PALÁDIO, HIDROGENAÇÃO

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      COSTA, Natália de Jesus da Silva et al. Organometallic preparation of Ni, Pd, and NiPd nanoparticles for the design of supported nanocatalysts. ACS Catalysis, v. 4, n. 6, p. 1735-1742, 2014Tradução . . Disponível em: https://doi.org/10.1021/cs500337a. Acesso em: 01 maio 2024.
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      Costa, N. de J. da S., Guerrero, M., Collière, V., Teixeira Neto, É., Landers, R., Philippot, K., & Rossi, L. M. (2014). Organometallic preparation of Ni, Pd, and NiPd nanoparticles for the design of supported nanocatalysts. ACS Catalysis, 4( 6), 1735-1742. doi:10.1021/cs500337a
    • NLM

      Costa N de J da S, Guerrero M, Collière V, Teixeira Neto É, Landers R, Philippot K, Rossi LM. Organometallic preparation of Ni, Pd, and NiPd nanoparticles for the design of supported nanocatalysts [Internet]. ACS Catalysis. 2014 ; 4( 6): 1735-1742.[citado 2024 maio 01 ] Available from: https://doi.org/10.1021/cs500337a
    • Vancouver

      Costa N de J da S, Guerrero M, Collière V, Teixeira Neto É, Landers R, Philippot K, Rossi LM. Organometallic preparation of Ni, Pd, and NiPd nanoparticles for the design of supported nanocatalysts [Internet]. ACS Catalysis. 2014 ; 4( 6): 1735-1742.[citado 2024 maio 01 ] Available from: https://doi.org/10.1021/cs500337a
  • Source: Green Chemistry. Unidade: IQ

    Subjects: HIDROGENAÇÃO, QUÍMICA INORGÂNICA

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      UBERMAN, Paula M et al. A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model. Green Chemistry, v. 16, p. 4566-4574, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4gc00669k. Acesso em: 01 maio 2024.
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      Uberman, P. M., Costa, N. J. S., Philippot, K., Carmona, R. C., Santos, A. A. dos, & Rossi, L. M. (2014). A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model. Green Chemistry, 16, 4566-4574. doi:10.1039/c4gc00669k
    • NLM

      Uberman PM, Costa NJS, Philippot K, Carmona RC, Santos AA dos, Rossi LM. A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model [Internet]. Green Chemistry. 2014 ; 16 4566-4574.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/c4gc00669k
    • Vancouver

      Uberman PM, Costa NJS, Philippot K, Carmona RC, Santos AA dos, Rossi LM. A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model [Internet]. Green Chemistry. 2014 ; 16 4566-4574.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/c4gc00669k
  • Source: Journal of Materials Chemistry A. Unidade: IQ

    Assunto: NANOPARTÍCULAS

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      GUERRERO, Miguel et al. Taking advantage of a terpyridine ligand for the deposition of Pd nanoparticles onto a magnetic material for selective hydrogenation reactions†. Journal of Materials Chemistry A, v. 1, n. 4, p. 1441-1449, 2013Tradução . . Disponível em: https://doi.org/10.1039/c2ta00199c. Acesso em: 01 maio 2024.
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      Guerrero, M., Costa, N. de J. da S., Vono, L. L. R., Rossi, L. M., Gusevskaya, E. V., & Philippot, K. (2013). Taking advantage of a terpyridine ligand for the deposition of Pd nanoparticles onto a magnetic material for selective hydrogenation reactions†. Journal of Materials Chemistry A, 1( 4), 1441-1449. doi:10.1039/c2ta00199c
    • NLM

      Guerrero M, Costa N de J da S, Vono LLR, Rossi LM, Gusevskaya EV, Philippot K. Taking advantage of a terpyridine ligand for the deposition of Pd nanoparticles onto a magnetic material for selective hydrogenation reactions† [Internet]. Journal of Materials Chemistry A. 2013 ; 1( 4): 1441-1449.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/c2ta00199c
    • Vancouver

      Guerrero M, Costa N de J da S, Vono LLR, Rossi LM, Gusevskaya EV, Philippot K. Taking advantage of a terpyridine ligand for the deposition of Pd nanoparticles onto a magnetic material for selective hydrogenation reactions† [Internet]. Journal of Materials Chemistry A. 2013 ; 1( 4): 1441-1449.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/c2ta00199c
  • Source: Book Abstracts. Conference titles: Brazilian Meeting on Inorganic Chemistry (BMIC). Unidade: IQ

    Subjects: NANOPARTÍCULAS, CATÁLISE

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      ROSSI, Liane Marcia e COSTA, Natália de Jesus da Silva e PHILIPPOT, Karine. Advances in the design of nickel nanoparticle catalysts using an organometallic approach. 2012, Anais.. São Paulo: Sociedade Brasileira de Química (SBQ), 2012. . Acesso em: 01 maio 2024.
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      Rossi, L. M., Costa, N. de J. da S., & Philippot, K. (2012). Advances in the design of nickel nanoparticle catalysts using an organometallic approach. In Book Abstracts. São Paulo: Sociedade Brasileira de Química (SBQ).
    • NLM

      Rossi LM, Costa N de J da S, Philippot K. Advances in the design of nickel nanoparticle catalysts using an organometallic approach. Book Abstracts. 2012 ;[citado 2024 maio 01 ]
    • Vancouver

      Rossi LM, Costa N de J da S, Philippot K. Advances in the design of nickel nanoparticle catalysts using an organometallic approach. Book Abstracts. 2012 ;[citado 2024 maio 01 ]
  • Source: Journal of Catalysis. Unidades: IF, IQ

    Subjects: PALÁDIO, SEPARAÇÃO MAGNÉTICA, NANOPARTÍCULAS

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      COSTA, Natália de Jesus da Silva et al. A single-step procedure for the preparation of palladium nanoparticles and a phosphine-functionalized support as catalyst for Suzuki cross-coupling reactions. Journal of Catalysis, v. 276, n. 2, p. 382-389, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.jcat.2010.09.028. Acesso em: 01 maio 2024.
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      Costa, N. de J. da S., Kiyohara, P. K., Monteiro, A. L., Coppel, Y., Philippot, K., & Rossi, L. M. (2010). A single-step procedure for the preparation of palladium nanoparticles and a phosphine-functionalized support as catalyst for Suzuki cross-coupling reactions. Journal of Catalysis, 276( 2), 382-389. doi:10.1016/j.jcat.2010.09.028
    • NLM

      Costa N de J da S, Kiyohara PK, Monteiro AL, Coppel Y, Philippot K, Rossi LM. A single-step procedure for the preparation of palladium nanoparticles and a phosphine-functionalized support as catalyst for Suzuki cross-coupling reactions [Internet]. Journal of Catalysis. 2010 ; 276( 2): 382-389.[citado 2024 maio 01 ] Available from: https://doi.org/10.1016/j.jcat.2010.09.028
    • Vancouver

      Costa N de J da S, Kiyohara PK, Monteiro AL, Coppel Y, Philippot K, Rossi LM. A single-step procedure for the preparation of palladium nanoparticles and a phosphine-functionalized support as catalyst for Suzuki cross-coupling reactions [Internet]. Journal of Catalysis. 2010 ; 276( 2): 382-389.[citado 2024 maio 01 ] Available from: https://doi.org/10.1016/j.jcat.2010.09.028

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