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1 - 13 (13 records)

  • Artigo de periodico

    The molecular basis of organic Chemiluminescence (2023)

    Cabello, Maidileyvis Castro; Bartoloni, Fernando Heering ; Bastos, Erick Leite ; Baader, Wilhelm Josef

    Source: Biosensors. Unidade: IQ

    Subjects: LUMINESCÊNCIA, REAÇÕES QUÍMICAS, BIOLUMINESCÊNCIA

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      CABELLO, Maidileyvis Castro et al. The molecular basis of organic Chemiluminescence. Biosensors, v. 13, p. 1-21 art. 452, 2023Tradução . . Disponível em: https://doi.org/10.3390/bios13040452. Acesso em: 12 ago. 2024.

    • APA

      Cabello, M. C., Bartoloni, F. H., Bastos, E. L., & Baader, W. J. (2023). The molecular basis of organic Chemiluminescence. Biosensors, 13, 1-21 art. 452. doi:10.3390/bios13040452

    • NLM

      Cabello MC, Bartoloni FH, Bastos EL, Baader WJ. The molecular basis of organic Chemiluminescence [Internet]. Biosensors. 2023 ; 13 1-21 art. 452.[citado 2024 ago. 12 ] Available from: https://doi.org/10.3390/bios13040452

    • Vancouver

      Cabello MC, Bartoloni FH, Bastos EL, Baader WJ. The molecular basis of organic Chemiluminescence [Internet]. Biosensors. 2023 ; 13 1-21 art. 452.[citado 2024 ago. 12 ] Available from: https://doi.org/10.3390/bios13040452

  • Artigo de periodico

    Can single cell respiration be measured by scanning electrochemical microscopy (SECM)? (2023)

    Cremin, Kelsey; Meloni, Gabriel Negrão ; Valavanis, Dimitrios; Soyer, Orkun S; Unwin, Patrick R

    Source: ACS Measurement Science Au. Unidade: IQ

    Subjects: ELETROQUÍMICA, OXIGÊNIO, REAÇÕES QUÍMICAS

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      CREMIN, Kelsey et al. Can single cell respiration be measured by scanning electrochemical microscopy (SECM)?. ACS Measurement Science Au, v. 3, p. 361−370, 2023Tradução . . Disponível em: https://dx.doi.org/10.1021/acsmeasuresciau.3c00019. Acesso em: 12 ago. 2024.

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      Cremin, K., Meloni, G. N., Valavanis, D., Soyer, O. S., & Unwin, P. R. (2023). Can single cell respiration be measured by scanning electrochemical microscopy (SECM)? ACS Measurement Science Au, 3, 361−370. doi:10.1021/acsmeasuresciau.3c00019

    • NLM

      Cremin K, Meloni GN, Valavanis D, Soyer OS, Unwin PR. Can single cell respiration be measured by scanning electrochemical microscopy (SECM)? [Internet]. ACS Measurement Science Au. 2023 ; 3 361−370.[citado 2024 ago. 12 ] Available from: https://dx.doi.org/10.1021/acsmeasuresciau.3c00019

    • Vancouver

      Cremin K, Meloni GN, Valavanis D, Soyer OS, Unwin PR. Can single cell respiration be measured by scanning electrochemical microscopy (SECM)? [Internet]. ACS Measurement Science Au. 2023 ; 3 361−370.[citado 2024 ago. 12 ] Available from: https://dx.doi.org/10.1021/acsmeasuresciau.3c00019

  • Artigo de periodico

    Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions (2021)

    Sanabria, Marialy Nieves ; Andrade, Leandro Helgueira

    Source: ACS Sustainable Chemistry & Engineering. Unidade: IQ

    Subjects: COMPOSTOS AROMÁTICOS, SOLVENTE, REAÇÕES QUÍMICAS, RADIAÇÃO ELETROMAGNÉTICA, IRRADIAÇÃO

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      SANABRIA, Marialy Nieves e ANDRADE, Leandro Helgueira. Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions. ACS Sustainable Chemistry & Engineering, v. 9, n. 41, p. 13735-13741, 2021Tradução . . Disponível em: https://doi.org/10.1021/acssuschemeng.1c04077. Acesso em: 12 ago. 2024.

    • APA

      Sanabria, M. N., & Andrade, L. H. (2021). Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions. ACS Sustainable Chemistry & Engineering, 9( 41), 13735-13741. doi:10.1021/acssuschemeng.1c04077

    • NLM

      Sanabria MN, Andrade LH. Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions [Internet]. ACS Sustainable Chemistry & Engineering. 2021 ; 9( 41): 13735-13741.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1021/acssuschemeng.1c04077

    • Vancouver

      Sanabria MN, Andrade LH. Microwave irradiation and formamide: a perfect match for ultrafast carbamoylation via radical reactions [Internet]. ACS Sustainable Chemistry & Engineering. 2021 ; 9( 41): 13735-13741.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1021/acssuschemeng.1c04077

  • Artigo de periodico

    Limitations of teaching and learning redox: a systematic review (2020)

    Goes, Luciane F; Nogueira, keysy S. C; Fernandez, Carmen

    Source: Problems of Education in the 21st Century. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, ENSINO E APRENDIZAGEM

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      GOES, Luciane F e NOGUEIRA, keysy S. C e FERNANDEZ, Carmen. Limitations of teaching and learning redox: a systematic review. Problems of Education in the 21st Century, v. 78, n. 5, p. 698-718, 2020Tradução . . Disponível em: https://doi.org/10.33225/pec/20.78.698. Acesso em: 12 ago. 2024.

    • APA

      Goes, L. F., Nogueira, keysy S. C., & Fernandez, C. (2020). Limitations of teaching and learning redox: a systematic review. Problems of Education in the 21st Century, 78( 5), 698-718. doi:10.33225/pec/20.78.698

    • NLM

      Goes LF, Nogueira keysy SC, Fernandez C. Limitations of teaching and learning redox: a systematic review [Internet]. Problems of Education in the 21st Century. 2020 ; 78( 5): 698-718.[citado 2024 ago. 12 ] Available from: https://doi.org/10.33225/pec/20.78.698

    • Vancouver

      Goes LF, Nogueira keysy SC, Fernandez C. Limitations of teaching and learning redox: a systematic review [Internet]. Problems of Education in the 21st Century. 2020 ; 78( 5): 698-718.[citado 2024 ago. 12 ] Available from: https://doi.org/10.33225/pec/20.78.698

  • Artigo de periodico

    Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity (2020)

    Polo, Ellen Christine; Wang, Martí Fernández; Angnes, Ricardo Almir; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte

    Source: Advanced Synthesis and Catalysis. Unidade: IQ

    Subjects: CATÁLISE ASSIMÉTRICA, REAÇÕES QUÍMICAS, PALÁDIO

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    • ABNT

      POLO, Ellen Christine et al. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, v. 362, p. 884 – 892, 2020Tradução . . Disponível em: https://doi.org/10.1002/adsc.201901471. Acesso em: 12 ago. 2024.

    • APA

      Polo, E. C., Wang, M. F., Angnes, R. A., Braga, A. A. C., & Correia, C. R. D. (2020). Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, 362, 884 – 892. doi:10.1002/adsc.201901471

    • NLM

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/adsc.201901471

    • Vancouver

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/adsc.201901471

  • Artigo de periodico

    DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts (2019)

    Silva, Vitor Hugo Menezes da ; Morgon, Nelson H ; Correia, Carlos R. D ; Braga, Ataualpa Albert Carmo

    Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, SÍNTESE ORGÂNICA

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    • ABNT

      SILVA, Vitor Hugo Menezes da et al. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, v. 896, p. 5-15, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2019.05.023. Acesso em: 12 ago. 2024.

    • APA

      Silva, V. H. M. da, Morgon, N. H., Correia, C. R. D., & Braga, A. A. C. (2019). DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, 896, 5-15. doi:10.1016/j.jorganchem.2019.05.023

    • NLM

      Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023

    • Vancouver

      Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023

  • Artigo de periodico-divulgacao

    Theories of molecular reaction dfynamics: the microscopic foundation of chemical kinetics (2019)

    Camargo, Pedro Henrique Cury de

    Source: Journal of Materials Science. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, DINÂMICA, FÍSICA MOLECULAR

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      CAMARGO, Pedro Henrique Cury de. Theories of molecular reaction dfynamics: the microscopic foundation of chemical kinetics. Journal of Materials Science. New York: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1007/s10853-019-03671-w. Acesso em: 12 ago. 2024. , 2019

    • APA

      Camargo, P. H. C. de. (2019). Theories of molecular reaction dfynamics: the microscopic foundation of chemical kinetics. Journal of Materials Science. New York: Instituto de Química, Universidade de São Paulo. doi:10.1007/s10853-019-03671-w

    • NLM

      Camargo PHC de. Theories of molecular reaction dfynamics: the microscopic foundation of chemical kinetics [Internet]. Journal of Materials Science. 2019 ; 54( 15): 10595-10599.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1007/s10853-019-03671-w

    • Vancouver

      Camargo PHC de. Theories of molecular reaction dfynamics: the microscopic foundation of chemical kinetics [Internet]. Journal of Materials Science. 2019 ; 54( 15): 10595-10599.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1007/s10853-019-03671-w

  • Artigo de periodico

    Probe effects on concentration profiles in the diffusion layer: computational modeling and near-surface pH measurements using microelectrodes (2018)

    Critelli, Renan A. J; Bertotti, Mauro ; Torresi, Roberto Manuel

    Source: Electrochimica Acta. Unidade: IQ

    Subjects: ELETROQUÍMICA, REAÇÕES QUÍMICAS

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      CRITELLI, Renan A. J e BERTOTTI, Mauro e TORRESI, Roberto Manuel. Probe effects on concentration profiles in the diffusion layer: computational modeling and near-surface pH measurements using microelectrodes. Electrochimica Acta, v. 292, p. 511-521 , 2018Tradução . . Disponível em: https://doi.org/10.1016/j.electacta.2018.09.157. Acesso em: 12 ago. 2024.

    • APA

      Critelli, R. A. J., Bertotti, M., & Torresi, R. M. (2018). Probe effects on concentration profiles in the diffusion layer: computational modeling and near-surface pH measurements using microelectrodes. Electrochimica Acta, 292, 511-521 . doi:10.1016/j.electacta.2018.09.157

    • NLM

      Critelli RAJ, Bertotti M, Torresi RM. Probe effects on concentration profiles in the diffusion layer: computational modeling and near-surface pH measurements using microelectrodes [Internet]. Electrochimica Acta. 2018 ; 292 511-521 .[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.electacta.2018.09.157

    • Vancouver

      Critelli RAJ, Bertotti M, Torresi RM. Probe effects on concentration profiles in the diffusion layer: computational modeling and near-surface pH measurements using microelectrodes [Internet]. Electrochimica Acta. 2018 ; 292 511-521 .[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.electacta.2018.09.157

  • Artigo de periodico

    Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction (2017)

    Leitao, Ezequiel F. V; Ventura, Elizete; Souza, Miguel A. F. de; Riveros, José Manuel; Monte, Silmar A

    Source: ChemistryOpen. Unidade: IQ

    Subjects: FÍSICO-QUÍMICA, REAÇÕES QUÍMICAS

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      LEITAO, Ezequiel F. V et al. Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction. ChemistryOpen, v. 6, p. 360 –363, 2017Tradução . . Disponível em: https://doi.org/10.1002/open.201600169. Acesso em: 12 ago. 2024.

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      Leitao, E. F. V., Ventura, E., Souza, M. A. F. de, Riveros, J. M., & Monte, S. A. (2017). Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction. ChemistryOpen, 6, 360 –363. doi:10.1002/open.201600169

    • NLM

      Leitao EFV, Ventura E, Souza MAF de, Riveros JM, Monte SA. Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction [Internet]. ChemistryOpen. 2017 ; 6 360 –363.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/open.201600169

    • Vancouver

      Leitao EFV, Ventura E, Souza MAF de, Riveros JM, Monte SA. Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction [Internet]. ChemistryOpen. 2017 ; 6 360 –363.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/open.201600169

  • Artigo de periodico

    New insights into the electrophilic aromatic substitution mechanism of tricyanovinylation reaction involving tetracyanoethylene and N,N-dimethylaniline: an interpretation based on density functional theory calculations (2017)

    Silva, Vitor Hugo Menezes da; Monezi, Natália Mariana; Ando, Rômulo Augusto ; Braga, Ataualpa Albert Carmo

    Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, SOLVENTE

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      SILVA, Vitor Hugo Menezes da et al. New insights into the electrophilic aromatic substitution mechanism of tricyanovinylation reaction involving tetracyanoethylene and N,N-dimethylaniline: an interpretation based on density functional theory calculations. Journal of Molecular Structure, v. 1142, p. 58–65, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2017.04.053. Acesso em: 12 ago. 2024.

    • APA

      Silva, V. H. M. da, Monezi, N. M., Ando, R. A., & Braga, A. A. C. (2017). New insights into the electrophilic aromatic substitution mechanism of tricyanovinylation reaction involving tetracyanoethylene and N,N-dimethylaniline: an interpretation based on density functional theory calculations. Journal of Molecular Structure, 1142, 58–65. doi:10.1016/j.molstruc.2017.04.053

    • NLM

      Silva VHM da, Monezi NM, Ando RA, Braga AAC. New insights into the electrophilic aromatic substitution mechanism of tricyanovinylation reaction involving tetracyanoethylene and N,N-dimethylaniline: an interpretation based on density functional theory calculations [Internet]. Journal of Molecular Structure. 2017 ; 1142 58–65.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2017.04.053

    • Vancouver

      Silva VHM da, Monezi NM, Ando RA, Braga AAC. New insights into the electrophilic aromatic substitution mechanism of tricyanovinylation reaction involving tetracyanoethylene and N,N-dimethylaniline: an interpretation based on density functional theory calculations [Internet]. Journal of Molecular Structure. 2017 ; 1142 58–65.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.molstruc.2017.04.053

  • Trabalho de evento-resumo

    Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium (2017)

    Albuquerque, Gabriela Zuleide Correia; Vairolette, Lucas E; Rocha, Fernando; Goes, Luciane Fernandes de; Fernandez, Carmen ; Agostinho, Sílvia Maria Leite

    Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, FORMAÇÃO DE PROFESSORES, QUÍMICA

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      ALBUQUERQUE, Gabriela Zuleide Correia et al. Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 12 ago. 2024.

    • APA

      Albuquerque, G. Z. C., Vairolette, L. E., Rocha, F., Goes, L. F. de, Fernandez, C., & Agostinho, S. M. L. (2017). Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/

    • NLM

      Albuquerque GZC, Vairolette LE, Rocha F, Goes LF de, Fernandez C, Agostinho SML. Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium [Internet]. Proceedings. 2017 ;[citado 2024 ago. 12 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/

    • Vancouver

      Albuquerque GZC, Vairolette LE, Rocha F, Goes LF de, Fernandez C, Agostinho SML. Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium [Internet]. Proceedings. 2017 ;[citado 2024 ago. 12 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/

  • Artigo de periodico

    Resonance Raman and UV-VIS spectroscopic investigation of the reaction of tetracyanoethylene and N-methyldiphenylamine (2017)

    Monezi, Natália Mariana; Ando, Rômulo Augusto

    Source: Journal of Raman Spectroscopy. Unidade: IQ

    Subjects: ESPECTROSCOPIA RAMAN, REAÇÕES QUÍMICAS

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      MONEZI, Natália Mariana e ANDO, Rômulo Augusto. Resonance Raman and UV-VIS spectroscopic investigation of the reaction of tetracyanoethylene and N-methyldiphenylamine. Journal of Raman Spectroscopy, v. 48, n. 5, p. 758-764, 2017Tradução . . Disponível em: https://doi.org/10.1002/jrs.5091. Acesso em: 12 ago. 2024.

    • APA

      Monezi, N. M., & Ando, R. A. (2017). Resonance Raman and UV-VIS spectroscopic investigation of the reaction of tetracyanoethylene and N-methyldiphenylamine. Journal of Raman Spectroscopy, 48( 5), 758-764. doi:10.1002/jrs.5091

    • NLM

      Monezi NM, Ando RA. Resonance Raman and UV-VIS spectroscopic investigation of the reaction of tetracyanoethylene and N-methyldiphenylamine [Internet]. Journal of Raman Spectroscopy. 2017 ; 48( 5): 758-764.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/jrs.5091

    • Vancouver

      Monezi NM, Ando RA. Resonance Raman and UV-VIS spectroscopic investigation of the reaction of tetracyanoethylene and N-methyldiphenylamine [Internet]. Journal of Raman Spectroscopy. 2017 ; 48( 5): 758-764.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/jrs.5091

  • Artigo de periodico

    Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds (2016)

    Silva, Juliana de Oliveira; Angnes, Ricardo A; Silva, Vitor Hugo Menezes da; Servilha, Bruno M; Adeel, Muhammad; Braga, Ataualpa Albert Carmo ; Aponick, Aaron; Correia, Carlos Roque Duarte

    Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: SOLVENTE, CATÁLISE, REAÇÕES QUÍMICAS

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      SILVA, Juliana de Oliveira et al. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, v. 81, n. 5, p. 2010-2018, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b02846. Acesso em: 12 ago. 2024.

    • APA

      Silva, J. de O., Angnes, R. A., Silva, V. H. M. da, Servilha, B. M., Adeel, M., Braga, A. A. C., et al. (2016). Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, 81( 5), 2010-2018. doi:10.1021/acs.joc.5b02846

    • NLM

      Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1021/acs.joc.5b02846

    • Vancouver

      Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1021/acs.joc.5b02846
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