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  • Source: Chemical Communications. Unidade: IQSC

    Subjects: HIDROGÊNIO, SACARÍDEOS

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      IOST, Rodrigo M et al. Hydrogen bioelectrogeneration with pH-resilient and oxygen-tolerant cobalt apoenzyme-saccharide. Chemical Communications, v. 60, p. 2509, 2024Tradução . . Disponível em: https://doi.org/ 10.1039/d3cc06185j. Acesso em: 26 abr. 2024.
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      Iost, R. M., Venkatkarthick, R., Nascimento, S. Q., Lima, F. H. B. de, & Crespilho, F. N. (2024). Hydrogen bioelectrogeneration with pH-resilient and oxygen-tolerant cobalt apoenzyme-saccharide. Chemical Communications, 60, 2509. doi:10.1039/d3cc06185j
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      Iost RM, Venkatkarthick R, Nascimento SQ, Lima FHB de, Crespilho FN. Hydrogen bioelectrogeneration with pH-resilient and oxygen-tolerant cobalt apoenzyme-saccharide [Internet]. Chemical Communications. 2024 ;60 2509.[citado 2024 abr. 26 ] Available from: https://doi.org/ 10.1039/d3cc06185j
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      Iost RM, Venkatkarthick R, Nascimento SQ, Lima FHB de, Crespilho FN. Hydrogen bioelectrogeneration with pH-resilient and oxygen-tolerant cobalt apoenzyme-saccharide [Internet]. Chemical Communications. 2024 ;60 2509.[citado 2024 abr. 26 ] Available from: https://doi.org/ 10.1039/d3cc06185j
  • Source: Chemical Communications. Unidade: IQSC

    Subjects: PEPTÍDEOS, ALQUILAÇÃO, FOTOCATÁLISE

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      LIMA, Rafaely N. et al. Post-synthetic functionalization of tryptophan protected peptide sequences through indole (C-2) photocatalytic alkylation. Chemical Communications, v. 57, p. 5758–5761, 2021Tradução . . Disponível em: https://doi.org/10.1039/d1cc01822a. Acesso em: 26 abr. 2024.
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      Lima, R. N., Delgado, J. A. C., Bernardi, D. I., Berlinck, R. G. de S., Kaplaneris, N., Ackermann, L., & Paixão, M. W. (2021). Post-synthetic functionalization of tryptophan protected peptide sequences through indole (C-2) photocatalytic alkylation. Chemical Communications, 57, 5758–5761. doi:10.1039/d1cc01822a
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      Lima RN, Delgado JAC, Bernardi DI, Berlinck RG de S, Kaplaneris N, Ackermann L, Paixão MW. Post-synthetic functionalization of tryptophan protected peptide sequences through indole (C-2) photocatalytic alkylation [Internet]. Chemical Communications. 2021 ; 57 5758–5761.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d1cc01822a
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      Lima RN, Delgado JAC, Bernardi DI, Berlinck RG de S, Kaplaneris N, Ackermann L, Paixão MW. Post-synthetic functionalization of tryptophan protected peptide sequences through indole (C-2) photocatalytic alkylation [Internet]. Chemical Communications. 2021 ; 57 5758–5761.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d1cc01822a
  • Source: Chemical Communications. Unidade: FCF

    Subjects: ESPECTROSCOPIA, ANTIBIÓTICOS

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      DEMARQUE, Daniel Pecoraro e KEMPER, Michael e MERTEN, Christian. VCD spectroscopy reveals that a water molecule determines the conformation of azithromycin in solution. Chemical Communications, v. 57, p. 4031–4034, 2021Tradução . . Disponível em: https://doi.org/10.1039/d1cc00932j. Acesso em: 26 abr. 2024.
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      Demarque, D. P., Kemper, M., & Merten, C. (2021). VCD spectroscopy reveals that a water molecule determines the conformation of azithromycin in solution. Chemical Communications, 57, 4031–4034. doi:10.1039/d1cc00932j
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      Demarque DP, Kemper M, Merten C. VCD spectroscopy reveals that a water molecule determines the conformation of azithromycin in solution [Internet]. Chemical Communications. 2021 ; 57 4031–4034.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d1cc00932j
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      Demarque DP, Kemper M, Merten C. VCD spectroscopy reveals that a water molecule determines the conformation of azithromycin in solution [Internet]. Chemical Communications. 2021 ; 57 4031–4034.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d1cc00932j
  • Source: Chemical Communications. Unidade: IQ

    Subjects: ESPECTROSCOPIA, NANOPARTÍCULAS, OURO

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      OLIVEIRA, Paulo Filho Marques de et al. Tandem X-ray absorption spectroscopy and scattering for in situ time-resolved monitoring of gold nanoparticle mechanosynthesis. Chemical Communications, v. 56, p. 10329-10332, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0cc03862h. Acesso em: 26 abr. 2024.
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      Oliveira, P. F. M. de, Michalchuk, A. A. L., Buzanich, A. G., Bienert, R., Torresi, R. M., Camargo, P. H. C. de, & Emmerling, F. (2020). Tandem X-ray absorption spectroscopy and scattering for in situ time-resolved monitoring of gold nanoparticle mechanosynthesis. Chemical Communications, 56, 10329-10332. doi:10.1039/d0cc03862h
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      Oliveira PFM de, Michalchuk AAL, Buzanich AG, Bienert R, Torresi RM, Camargo PHC de, Emmerling F. Tandem X-ray absorption spectroscopy and scattering for in situ time-resolved monitoring of gold nanoparticle mechanosynthesis [Internet]. Chemical Communications. 2020 ; 56 10329-10332.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc03862h
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      Oliveira PFM de, Michalchuk AAL, Buzanich AG, Bienert R, Torresi RM, Camargo PHC de, Emmerling F. Tandem X-ray absorption spectroscopy and scattering for in situ time-resolved monitoring of gold nanoparticle mechanosynthesis [Internet]. Chemical Communications. 2020 ; 56 10329-10332.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc03862h
  • Source: Chemical Communications. Unidade: IQ

    Subjects: ELETROQUÍMICA, SILÍCIO

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      GAUTAM, Shreedhar et al. High-resolution light-activated electrochemistry on amorphous silicon-based photoelectrodes. Chemical Communications, v. 56, p. 7435-7438, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0cc02959a. Acesso em: 26 abr. 2024.
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      Gautam, S., Gonçales, V. R., Colombo, R. N. P., Tang, W., Torresi, S. I. C. de, Reece, P. J., et al. (2020). High-resolution light-activated electrochemistry on amorphous silicon-based photoelectrodes. Chemical Communications, 56, 7435-7438. doi:10.1039/d0cc02959a
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      Gautam S, Gonçales VR, Colombo RNP, Tang W, Torresi SIC de, Reece PJ, Tilley RD, Gooding JJ. High-resolution light-activated electrochemistry on amorphous silicon-based photoelectrodes [Internet]. Chemical Communications. 2020 ; 56 7435-7438.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc02959a
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      Gautam S, Gonçales VR, Colombo RNP, Tang W, Torresi SIC de, Reece PJ, Tilley RD, Gooding JJ. High-resolution light-activated electrochemistry on amorphous silicon-based photoelectrodes [Internet]. Chemical Communications. 2020 ; 56 7435-7438.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc02959a
  • Source: Chemical Communications. Unidades: IQ, IFSC

    Subjects: BIOCOMBUSTÍVEIS, CARBONO

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      SEMPIONATTO, Juliane Renata et al. Enzymatic biofuel cells based on protective hydrophobic carbon paste electrodes: towards epidermal bioenergy harvesting in the acidic sweat environment. Chemical Communications, v. 56, n. 13, p. 2004-2007, 2020Tradução . . Disponível em: https://doi.org/10.1039/c9cc09533k. Acesso em: 26 abr. 2024.
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      Sempionatto, J. R., Raymundo-Pereira, P. A., Azeredo, N. F. B., Silva, A. N. D. L. e, Angnes, L., & Wang, J. (2020). Enzymatic biofuel cells based on protective hydrophobic carbon paste electrodes: towards epidermal bioenergy harvesting in the acidic sweat environment. Chemical Communications, 56( 13), 2004-2007. doi:10.1039/c9cc09533k
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      Sempionatto JR, Raymundo-Pereira PA, Azeredo NFB, Silva ANDL e, Angnes L, Wang J. Enzymatic biofuel cells based on protective hydrophobic carbon paste electrodes: towards epidermal bioenergy harvesting in the acidic sweat environment [Internet]. Chemical Communications. 2020 ; 56( 13): 2004-2007.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c9cc09533k
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      Sempionatto JR, Raymundo-Pereira PA, Azeredo NFB, Silva ANDL e, Angnes L, Wang J. Enzymatic biofuel cells based on protective hydrophobic carbon paste electrodes: towards epidermal bioenergy harvesting in the acidic sweat environment [Internet]. Chemical Communications. 2020 ; 56( 13): 2004-2007.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c9cc09533k
  • Source: Chemical Communications. Unidade: IQ

    Subjects: ELETRODEPOSIÇÃO, ESPECTROSCOPIA RAMAN

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      COLOMBO, Rafael Neri Prystaj et al. Spatially localized electrodeposition of multiple metals via light-activated electrochemistry for surface enhanced Raman spectroscopy applications. Chemical Communications, v. 56, p. 5831-5834, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0cc01661f. Acesso em: 26 abr. 2024.
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      Colombo, R. N. P., Gonçales, V. R., Gautam, S., Tilley, R., Gooding, J. J., & Torresi, S. I. C. de. (2020). Spatially localized electrodeposition of multiple metals via light-activated electrochemistry for surface enhanced Raman spectroscopy applications. Chemical Communications, 56, 5831-5834. doi:10.1039/d0cc01661f
    • NLM

      Colombo RNP, Gonçales VR, Gautam S, Tilley R, Gooding JJ, Torresi SIC de. Spatially localized electrodeposition of multiple metals via light-activated electrochemistry for surface enhanced Raman spectroscopy applications [Internet]. Chemical Communications. 2020 ; 56 5831-5834.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc01661f
    • Vancouver

      Colombo RNP, Gonçales VR, Gautam S, Tilley R, Gooding JJ, Torresi SIC de. Spatially localized electrodeposition of multiple metals via light-activated electrochemistry for surface enhanced Raman spectroscopy applications [Internet]. Chemical Communications. 2020 ; 56 5831-5834.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc01661f
  • Source: Chemical Communications. Unidade: IFSC

    Subjects: LIPOSSOMOS, NANOPARTÍCULAS

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      RIBOVSKI, Laís et al. Light-induced molecular rotation triggers on-demand release from liposomes. Chemical Communications, v. 56, n. 62, p. 8774-8777, 2020Tradução . . Disponível em: https://doi.org/10.1039/D0CC02499F. Acesso em: 26 abr. 2024.
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      Ribovski, L., Zhou, Q., Chen, J., Feringa, B. L., Rijn, P. van, & Zuhorn, I. S. (2020). Light-induced molecular rotation triggers on-demand release from liposomes. Chemical Communications, 56( 62), 8774-8777. doi:10.1039/D0CC02499F
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      Ribovski L, Zhou Q, Chen J, Feringa BL, Rijn P van, Zuhorn IS. Light-induced molecular rotation triggers on-demand release from liposomes [Internet]. Chemical Communications. 2020 ; 56( 62): 8774-8777.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/D0CC02499F
    • Vancouver

      Ribovski L, Zhou Q, Chen J, Feringa BL, Rijn P van, Zuhorn IS. Light-induced molecular rotation triggers on-demand release from liposomes [Internet]. Chemical Communications. 2020 ; 56( 62): 8774-8777.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/D0CC02499F
  • Source: Chemical Communications. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, CARBONO (ESTRUTURA;ESTUDO), QUÍMICA INORGÂNICA

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      SANTOS, Fernando Machado dos et al. A giant hybrid organic-inorganic octahedron from a narrow rim carboxylate calixarene. Chemical Communications, v. 56, n. 95, p. 15024-15027, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0cc07043b. Acesso em: 26 abr. 2024.
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      Santos, F. M. dos, Alvarenga, M. E., Valdo, A. K. S. M., Rabelo, R., Gomes, D. C. de C., Fátima, Â. de, et al. (2020). A giant hybrid organic-inorganic octahedron from a narrow rim carboxylate calixarene. Chemical Communications, 56( 95), 15024-15027. doi:10.1039/d0cc07043b
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      Santos FM dos, Alvarenga ME, Valdo AKSM, Rabelo R, Gomes DC de C, Fátima  de, Lara TVC, Silva CM da, Tasso TT, Araujo Neto JH, Batista AA, Ayala AP, Ellena J, Guimarães VF, Oliveira CMA, Silva LC da, Vaz BG, Martins FT. A giant hybrid organic-inorganic octahedron from a narrow rim carboxylate calixarene [Internet]. Chemical Communications. 2020 ; 56( 95): 15024-15027.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc07043b
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      Santos FM dos, Alvarenga ME, Valdo AKSM, Rabelo R, Gomes DC de C, Fátima  de, Lara TVC, Silva CM da, Tasso TT, Araujo Neto JH, Batista AA, Ayala AP, Ellena J, Guimarães VF, Oliveira CMA, Silva LC da, Vaz BG, Martins FT. A giant hybrid organic-inorganic octahedron from a narrow rim carboxylate calixarene [Internet]. Chemical Communications. 2020 ; 56( 95): 15024-15027.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/d0cc07043b
  • Source: Chemical Communications. Unidades: ICB, FCFRP, IO, IQSC

    Subjects: ANTHOZOA, ESPECTROMETRIA DE MASSAS, METABOLÔMICA, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)

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      LOTUFO, Leticia Veras Costa et al. Chemical profiling of two congeneric sea mat corals along the Brazilian coast: adaptive and functional patterns. Chemical Communications, v. 54, n. 16, p. 1952-1955, 2018Tradução . . Disponível em: https://doi.org/10.1039/c7cc08411k. Acesso em: 26 abr. 2024.
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      Lotufo, L. V. C., Carnevale Neto, F., Trindade-Silva, A. E., Silva, R. R. da, Silva, G. G. Z., Wilke, D. V., et al. (2018). Chemical profiling of two congeneric sea mat corals along the Brazilian coast: adaptive and functional patterns. Chemical Communications, 54( 16), 1952-1955. doi:10.1039/c7cc08411k
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      Lotufo LVC, Carnevale Neto F, Trindade-Silva AE, Silva RR da, Silva GGZ, Wilke DV, Pinto F das CL, Sahm BDB, Jimenez PC, Silva JNMG, Lotufo TM da C, Pessoa ODL, Lopes NP. Chemical profiling of two congeneric sea mat corals along the Brazilian coast: adaptive and functional patterns [Internet]. Chemical Communications. 2018 ; 54( 16): 1952-1955.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c7cc08411k
    • Vancouver

      Lotufo LVC, Carnevale Neto F, Trindade-Silva AE, Silva RR da, Silva GGZ, Wilke DV, Pinto F das CL, Sahm BDB, Jimenez PC, Silva JNMG, Lotufo TM da C, Pessoa ODL, Lopes NP. Chemical profiling of two congeneric sea mat corals along the Brazilian coast: adaptive and functional patterns [Internet]. Chemical Communications. 2018 ; 54( 16): 1952-1955.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c7cc08411k
  • Source: Chemical Communications. Unidade: IFSC

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, PROTEÍNAS (ESTUDO), PEPTÍDEOS

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      CAVINI, Italo A. et al. Inhibition of amyloid Aβ aggregation by high pressures or specific D-enantiomeric peptides. Chemical Communications, v. 54, n. 26, p. 3294-3297, 2018Tradução . . Disponível em: https://doi.org/10.1039/C8CC01458B. Acesso em: 26 abr. 2024.
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      Cavini, I. A., Munte, C. E., Erlach, M. B., Groen, T. van, Kadish, I., Zhang, T., et al. (2018). Inhibition of amyloid Aβ aggregation by high pressures or specific D-enantiomeric peptides. Chemical Communications, 54( 26), 3294-3297. doi:10.1039/C8CC01458B
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      Cavini IA, Munte CE, Erlach MB, Groen T van, Kadish I, Zhang T, Ziehm T, Nagel-Steger L, Kutzsche J, Kremer W, Willbold D, Kalbitzer HR. Inhibition of amyloid Aβ aggregation by high pressures or specific D-enantiomeric peptides [Internet]. Chemical Communications. 2018 ; 54( 26): 3294-3297.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/C8CC01458B
    • Vancouver

      Cavini IA, Munte CE, Erlach MB, Groen T van, Kadish I, Zhang T, Ziehm T, Nagel-Steger L, Kutzsche J, Kremer W, Willbold D, Kalbitzer HR. Inhibition of amyloid Aβ aggregation by high pressures or specific D-enantiomeric peptides [Internet]. Chemical Communications. 2018 ; 54( 26): 3294-3297.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/C8CC01458B
  • Source: Chemical Communications. Unidade: IQSC

    Assunto: ELETROCATÁLISE

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      KHALID, Mohd et al. Nano-flocks of bimetallic organic framework for efficient hydrogen evolution electrocatalysis. Chemical Communications, v. 54, p. 11048-11051, 2018Tradução . . Disponível em: http://pubs-rsc-org.ez67.periodicos.capes.gov.br/en/content/articlepdf/2018/cc/c8cc06918b?page=search. Acesso em: 26 abr. 2024.
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      Khalid, M., Hassan, A., Honorato, A. M. B., Crespilho, F. N., & Varela, H. (2018). Nano-flocks of bimetallic organic framework for efficient hydrogen evolution electrocatalysis. Chemical Communications, 54, 11048-11051. doi:10.1039/c8cc06918b
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      Khalid M, Hassan A, Honorato AMB, Crespilho FN, Varela H. Nano-flocks of bimetallic organic framework for efficient hydrogen evolution electrocatalysis [Internet]. Chemical Communications. 2018 ;54 11048-11051.[citado 2024 abr. 26 ] Available from: http://pubs-rsc-org.ez67.periodicos.capes.gov.br/en/content/articlepdf/2018/cc/c8cc06918b?page=search
    • Vancouver

      Khalid M, Hassan A, Honorato AMB, Crespilho FN, Varela H. Nano-flocks of bimetallic organic framework for efficient hydrogen evolution electrocatalysis [Internet]. Chemical Communications. 2018 ;54 11048-11051.[citado 2024 abr. 26 ] Available from: http://pubs-rsc-org.ez67.periodicos.capes.gov.br/en/content/articlepdf/2018/cc/c8cc06918b?page=search
  • Source: Chemical Communications. Unidade: IQ

    Subjects: DIFRAÇÃO POR RAIOS X, QUÍMICA DE COORDENAÇÃO

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      SURBELLA, Robert G et al. A new Pu(III) coordination geometry in ('C IND. 5''H IND. 5'NBr)'IND. 2'['PuCl IND. 3'('H IND. 2'O)'IND. 5']·2Cl·'2H IND. 2'O as obtained via supramolecular assembly in aqueous, high chloride media. Chemical Communications, v. 53, n. 78, p. 10816-10819, 2017Tradução . . Disponível em: https://doi.org/10.1039/C7CC05988D. Acesso em: 26 abr. 2024.
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      Surbella, R. G., Ducati, L. C., Pellegrini, K. L., McNamara, B. K., Autschbach, J., Schwantes, J. M., & Cahill, C. L. (2017). A new Pu(III) coordination geometry in ('C IND. 5''H IND. 5'NBr)'IND. 2'['PuCl IND. 3'('H IND. 2'O)'IND. 5']·2Cl·'2H IND. 2'O as obtained via supramolecular assembly in aqueous, high chloride media. Chemical Communications, 53( 78), 10816-10819. doi:10.1039/C7CC05988D
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      Surbella RG, Ducati LC, Pellegrini KL, McNamara BK, Autschbach J, Schwantes JM, Cahill CL. A new Pu(III) coordination geometry in ('C IND. 5''H IND. 5'NBr)'IND. 2'['PuCl IND. 3'('H IND. 2'O)'IND. 5']·2Cl·'2H IND. 2'O as obtained via supramolecular assembly in aqueous, high chloride media [Internet]. Chemical Communications. 2017 ; 53( 78): 10816-10819.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/C7CC05988D
    • Vancouver

      Surbella RG, Ducati LC, Pellegrini KL, McNamara BK, Autschbach J, Schwantes JM, Cahill CL. A new Pu(III) coordination geometry in ('C IND. 5''H IND. 5'NBr)'IND. 2'['PuCl IND. 3'('H IND. 2'O)'IND. 5']·2Cl·'2H IND. 2'O as obtained via supramolecular assembly in aqueous, high chloride media [Internet]. Chemical Communications. 2017 ; 53( 78): 10816-10819.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/C7CC05988D
  • Source: Chemical Communications. Unidade: IQ

    Subjects: NANOTECNOLOGIA, MATERIAIS NANOESTRUTURADOS, CATÁLISE

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      SILVA, Anderson G. M. da et al. Galvanic replacement reaction: recent developments for engineering metal nanostructures towards catalytic applications. Chemical Communications, v. 53, p. 7135-7148, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7cc02352a. Acesso em: 26 abr. 2024.
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      Silva, A. G. M. da, Rodrigues, T. S., Haigh, S. J., & Camargo, P. H. C. de. (2017). Galvanic replacement reaction: recent developments for engineering metal nanostructures towards catalytic applications. Chemical Communications, 53, 7135-7148. doi:10.1039/c7cc02352a
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      Silva AGM da, Rodrigues TS, Haigh SJ, Camargo PHC de. Galvanic replacement reaction: recent developments for engineering metal nanostructures towards catalytic applications [Internet]. Chemical Communications. 2017 ; 53 7135-7148.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c7cc02352a
    • Vancouver

      Silva AGM da, Rodrigues TS, Haigh SJ, Camargo PHC de. Galvanic replacement reaction: recent developments for engineering metal nanostructures towards catalytic applications [Internet]. Chemical Communications. 2017 ; 53 7135-7148.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c7cc02352a
  • Source: Chemical Communications. Unidades: IQ, IF

    Subjects: NANOTECNOLOGIA, LUMINESCÊNCIA

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      MORAIS, Alysson Ferreira et al. Hierarchical self-supported ZnAlEu LDH nanotubes hosting luminescent CdTe quantum dots. Chemical Communications, v. 53, p. 7341-7344 : + supplementary materials (S1-S9), 2017Tradução . . Disponível em: https://doi.org/10.1039/c7cc02097j. Acesso em: 26 abr. 2024.
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      Morais, A. F., Silva, I. G. N. da, Sree, S. P., Melo, F. M. de, Brabants, G., Brito, H. F. de, et al. (2017). Hierarchical self-supported ZnAlEu LDH nanotubes hosting luminescent CdTe quantum dots. Chemical Communications, 53, 7341-7344 : + supplementary materials (S1-S9). doi:10.1039/c7cc02097j
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      Morais AF, Silva IGN da, Sree SP, Melo FM de, Brabants G, Brito HF de, Martens JA, Toma HE, Kirschhock CEA, Breynaert E, Mustafa D. Hierarchical self-supported ZnAlEu LDH nanotubes hosting luminescent CdTe quantum dots [Internet]. Chemical Communications. 2017 ; 53 7341-7344 : + supplementary materials (S1-S9).[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c7cc02097j
    • Vancouver

      Morais AF, Silva IGN da, Sree SP, Melo FM de, Brabants G, Brito HF de, Martens JA, Toma HE, Kirschhock CEA, Breynaert E, Mustafa D. Hierarchical self-supported ZnAlEu LDH nanotubes hosting luminescent CdTe quantum dots [Internet]. Chemical Communications. 2017 ; 53 7341-7344 : + supplementary materials (S1-S9).[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c7cc02097j
  • Source: Chemical Communications. Unidade: IQ

    Assunto: NANOCOMPOSITOS

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      ZAMARION, Vitor de Moraes et al. Photonic metal-polymer resin nanocomposites with chiral nematic order. Chemical Communications, v. 52, n. 50, p. 7810-7813, 2016Tradução . . Disponível em: https://doi.org/10.1039/c6cc03147a. Acesso em: 26 abr. 2024.
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      Zamarion, V. de M., Khan, M. K., Schlesinger, M., Bsoul, A., Walus, K., Hamad, W. Y., & MacLachlan, M. J. (2016). Photonic metal-polymer resin nanocomposites with chiral nematic order. Chemical Communications, 52( 50), 7810-7813. doi:10.1039/c6cc03147a
    • NLM

      Zamarion V de M, Khan MK, Schlesinger M, Bsoul A, Walus K, Hamad WY, MacLachlan MJ. Photonic metal-polymer resin nanocomposites with chiral nematic order [Internet]. Chemical Communications. 2016 ; 52( 50): 7810-7813.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c6cc03147a
    • Vancouver

      Zamarion V de M, Khan MK, Schlesinger M, Bsoul A, Walus K, Hamad WY, MacLachlan MJ. Photonic metal-polymer resin nanocomposites with chiral nematic order [Internet]. Chemical Communications. 2016 ; 52( 50): 7810-7813.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c6cc03147a
  • Source: Chemical Communications. Unidade: IQSC

    Assunto: BIOMASSA

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      METZKER, Gustavo e BURTOLOSO, Antonio Carlos Bender. Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst. Chemical Communications, v. 51, n. 75, p. 14199-14202, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5cc02993g. Acesso em: 26 abr. 2024.
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      Metzker, G., & Burtoloso, A. C. B. (2015). Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst. Chemical Communications, 51( 75), 14199-14202. doi:10.1039/c5cc02993g
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      Metzker G, Burtoloso ACB. Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst [Internet]. Chemical Communications. 2015 ; 51( 75): 14199-14202.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c5cc02993g
    • Vancouver

      Metzker G, Burtoloso ACB. Conversion of levulinic acid into y-valerolactone using Fe(3)(CO)12: mimicking a biorefinery setting by exploiting crude liquos from biomass acid hydrolyst [Internet]. Chemical Communications. 2015 ; 51( 75): 14199-14202.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c5cc02993g
  • Source: Chemical Communications. Unidade: IFSC

    Subjects: VIDROS METÁLICOS, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      TRICOT, G. et al. P-O-B3 linkages in borophosphate glasses evidenced by high field 11B/31P correlation NMR. Chemical Communications, v. 51, n. 45, p. 9284-9286, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5cc01992c. Acesso em: 26 abr. 2024.
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      Tricot, G., Raguenet, B., Silly, G., Ribes, M., Pradel, A., & Eckert, H. (2015). P-O-B3 linkages in borophosphate glasses evidenced by high field 11B/31P correlation NMR. Chemical Communications, 51( 45), 9284-9286. doi:10.1039/c5cc01992c
    • NLM

      Tricot G, Raguenet B, Silly G, Ribes M, Pradel A, Eckert H. P-O-B3 linkages in borophosphate glasses evidenced by high field 11B/31P correlation NMR [Internet]. Chemical Communications. 2015 ; 51( 45): 9284-9286.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c5cc01992c
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      Tricot G, Raguenet B, Silly G, Ribes M, Pradel A, Eckert H. P-O-B3 linkages in borophosphate glasses evidenced by high field 11B/31P correlation NMR [Internet]. Chemical Communications. 2015 ; 51( 45): 9284-9286.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c5cc01992c
  • Source: Chemical Communications. Unidade: CENA

    Subjects: ESPECTROSCOPIA DE RAIO X, COBRE

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      GÜNTER, Tobias et al. Structural snapshots of the SCR reaction mechanism on Cu-SSZ-13. Chemical Communications, v. 51, p. 9227-9230, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5cc01758k. Acesso em: 26 abr. 2024.
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      Günter, T., Carvalho, H. W. P. de, Doronkin, D. E., Sheppard, T., Glatzel, P., Atkins, A. J., et al. (2015). Structural snapshots of the SCR reaction mechanism on Cu-SSZ-13. Chemical Communications, 51, 9227-9230. doi:10.1039/c5cc01758k
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      Günter T, Carvalho HWP de, Doronkin DE, Sheppard T, Glatzel P, Atkins AJ, Rudolph J, Jacob CR, Casapu M, Grunwaldt J-D. Structural snapshots of the SCR reaction mechanism on Cu-SSZ-13 [Internet]. Chemical Communications. 2015 ; 51 9227-9230.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c5cc01758k
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      Günter T, Carvalho HWP de, Doronkin DE, Sheppard T, Glatzel P, Atkins AJ, Rudolph J, Jacob CR, Casapu M, Grunwaldt J-D. Structural snapshots of the SCR reaction mechanism on Cu-SSZ-13 [Internet]. Chemical Communications. 2015 ; 51 9227-9230.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c5cc01758k
  • Source: Chemical Communications. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA

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      UTAKA, Aline e CAVALCANTI, Livia N e SILVA JUNIOR, Luiz Fernando da. Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, v. 50, n. 29, p. 3810-3813, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4cc00608a. Acesso em: 26 abr. 2024.
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      Utaka, A., Cavalcanti, L. N., & Silva Junior, L. F. da. (2014). Electrophilic alkynylation of ketones using hypervalent iodine. Chemical Communications, 50( 29), 3810-3813. doi:10.1039/c4cc00608a
    • NLM

      Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c4cc00608a
    • Vancouver

      Utaka A, Cavalcanti LN, Silva Junior LF da. Electrophilic alkynylation of ketones using hypervalent iodine [Internet]. Chemical Communications. 2014 ; 50( 29): 3810-3813.[citado 2024 abr. 26 ] Available from: https://doi.org/10.1039/c4cc00608a

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