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Dissertação (Mestrado)
Síntese por ultrassom da bambus[6]urila e estudo de suas propriedades físico-químicas (2017)
Cicolani, Renato Salviato; Demets, Gregoire Jean Francois (Orientador)
Unidade: FFCLRP
Subjects: SOLUBILIDADE, TEMPERATURA, REAÇÕES QUÍMICAS, QUÍMICA
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ABNT
CICOLANI, Renato Salviato. Síntese por ultrassom da bambus[6]urila e estudo de suas propriedades físico-químicas. 2017. Dissertação (Mestrado) – Universidade de São Paulo, Ribeirão Preto, 2017. Disponível em: http://www.teses.usp.br/teses/disponiveis/59/59138/tde-30082017-105639/. Acesso em: 12 ago. 2024.
APA
Cicolani, R. S. (2017). Síntese por ultrassom da bambus[6]urila e estudo de suas propriedades físico-químicas (Dissertação (Mestrado). Universidade de São Paulo, Ribeirão Preto. Recuperado de http://www.teses.usp.br/teses/disponiveis/59/59138/tde-30082017-105639/
NLM
Cicolani RS. Síntese por ultrassom da bambus[6]urila e estudo de suas propriedades físico-químicas [Internet]. 2017 ;[citado 2024 ago. 12 ] Available from: http://www.teses.usp.br/teses/disponiveis/59/59138/tde-30082017-105639/
Vancouver
Cicolani RS. Síntese por ultrassom da bambus[6]urila e estudo de suas propriedades físico-químicas [Internet]. 2017 ;[citado 2024 ago. 12 ] Available from: http://www.teses.usp.br/teses/disponiveis/59/59138/tde-30082017-105639/
Artigo de periodico
Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways (2017)
Baptista, Maurício da Silva ; Cadet, Jean; Di Mascio, Paolo ; Ghogare, Ashwini A; Greer, Alexander; Hamblin, Michael; Lorente, Carolina; Núñez, Silvia Cristina; Ribeiro, Martha Simões; Thomas, Andrés H; Vignoni, Mariana; Yoshimura, Tania Mateus
Source: Photochemistry and Photobiology. Unidade: IQ
Subjects: OXIDAÇÃO, REAÇÕES QUÍMICAS
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ABNT
BAPTISTA, Maurício da Silva et al. Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways. Photochemistry and Photobiology, v. 93, p. 912-919, 2017Tradução . . Disponível em: https://doi.org/10.1111/php.12716. Acesso em: 12 ago. 2024.
APA
Baptista, M. da S., Cadet, J., Di Mascio, P., Ghogare, A. A., Greer, A., Hamblin, M., et al. (2017). Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways. Photochemistry and Photobiology, 93, 912-919. doi:10.1111/php.12716
NLM
Baptista M da S, Cadet J, Di Mascio P, Ghogare AA, Greer A, Hamblin M, Lorente C, Núñez SC, Ribeiro MS, Thomas AH, Vignoni M, Yoshimura TM. Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways [Internet]. Photochemistry and Photobiology. 2017 ; 93 912-919.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1111/php.12716
Vancouver
Baptista M da S, Cadet J, Di Mascio P, Ghogare AA, Greer A, Hamblin M, Lorente C, Núñez SC, Ribeiro MS, Thomas AH, Vignoni M, Yoshimura TM. Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways [Internet]. Photochemistry and Photobiology. 2017 ; 93 912-919.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1111/php.12716
Artigo de periodico
A versatile and greener multicommuted flow-based system for exploiting relatively slow chemical reactions (2017)
Silva, Amanda R. M; Kamogawa, Marcos Yassuo; Melchert, Wanessa R
Source: Microchemical Journal. Unidade: ESALQ
Subjects: ANÁLISE POR INJEÇÃO EM FLUXO, ESPECTROFOTOMETRIA, REAÇÕES QUÍMICAS
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ABNT
SILVA, Amanda R. M e KAMOGAWA, Marcos Yassuo e MELCHERT, Wanessa R. A versatile and greener multicommuted flow-based system for exploiting relatively slow chemical reactions. Microchemical Journal, v. 133, p. 121-125, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.microc.2017.03.027. Acesso em: 12 ago. 2024.
APA
Silva, A. R. M., Kamogawa, M. Y., & Melchert, W. R. (2017). A versatile and greener multicommuted flow-based system for exploiting relatively slow chemical reactions. Microchemical Journal, 133, 121-125. doi:10.1016/j.microc.2017.03.027
NLM
Silva ARM, Kamogawa MY, Melchert WR. A versatile and greener multicommuted flow-based system for exploiting relatively slow chemical reactions [Internet]. Microchemical Journal. 2017 ; 133 121-125.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.microc.2017.03.027
Vancouver
Silva ARM, Kamogawa MY, Melchert WR. A versatile and greener multicommuted flow-based system for exploiting relatively slow chemical reactions [Internet]. Microchemical Journal. 2017 ; 133 121-125.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.microc.2017.03.027
Artigo de periodico
How computational methods and relativistic effects influence the study of chemical reactions involving Ru-NO complexes? (2017)
Orenha, Renato Pereira; Santiago, Regis Tadeu; Haiduke, Roberto Luiz Andrade ; Galembeck, Sérgio Emanuel
Source: Journal of computational chemistry. Unidades: IQSC, FFCLRP
Assunto: REAÇÕES QUÍMICAS
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ABNT
ORENHA, Renato Pereira et al. How computational methods and relativistic effects influence the study of chemical reactions involving Ru-NO complexes?. Journal of computational chemistry, v. 38, p. 883-891, 2017Tradução . . Disponível em: https://doi.org/10.1002/jcc.24762. Acesso em: 12 ago. 2024.
APA
Orenha, R. P., Santiago, R. T., Haiduke, R. L. A., & Galembeck, S. E. (2017). How computational methods and relativistic effects influence the study of chemical reactions involving Ru-NO complexes? Journal of computational chemistry, 38, 883-891. doi:10.1002/jcc.24762
NLM
Orenha RP, Santiago RT, Haiduke RLA, Galembeck SE. How computational methods and relativistic effects influence the study of chemical reactions involving Ru-NO complexes? [Internet]. Journal of computational chemistry. 2017 ; 38 883-891.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/jcc.24762
Vancouver
Orenha RP, Santiago RT, Haiduke RLA, Galembeck SE. How computational methods and relativistic effects influence the study of chemical reactions involving Ru-NO complexes? [Internet]. Journal of computational chemistry. 2017 ; 38 883-891.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1002/jcc.24762
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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ABNT
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.
APA
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
Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles (2017)
Ali, Bakhat; Vasconcelos, Stanley N. S; Shamim, Anwar; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre
Source: Arabian Journal of Chemistry. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS
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ABNT
ALI, Bakhat et al. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, v. 10, n. 4, p. 500-508, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.06.003. Acesso em: 12 ago. 2024.
APA
Ali, B., Vasconcelos, S. N. S., Shamim, A., Schpector, J. Z., & Stefani, H. A. (2017). Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, 10( 4), 500-508. doi:10.1016/j.arabjc.2016.06.003
NLM
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Vancouver
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
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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ABNT
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
Parte de monografia/livro
Reactions under ultrasound (2017)
Stefani, Hélio Alexandre ; Cella, Rodrigo
Source: Encyclopedia of Physical Organic Chemistry. Unidade: FCF
Subjects: REAÇÕES QUÍMICAS, FÍSICO-QUÍMICA ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre e CELLA, Rodrigo. Reactions under ultrasound. Encyclopedia of Physical Organic Chemistry. Tradução . Hoboken: Wiley, 2017. . . Acesso em: 12 ago. 2024.
APA
Stefani, H. A., & Cella, R. (2017). Reactions under ultrasound. In Encyclopedia of Physical Organic Chemistry. Hoboken: Wiley.
NLM
Stefani HA, Cella R. Reactions under ultrasound. In: Encyclopedia of Physical Organic Chemistry. Hoboken: Wiley; 2017. [citado 2024 ago. 12 ]
Vancouver
Stefani HA, Cella R. Reactions under ultrasound. In: Encyclopedia of Physical Organic Chemistry. Hoboken: Wiley; 2017. [citado 2024 ago. 12 ]
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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ABNT
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
New operational mode of an electrochemical reactor and its application to the degradation of levofloxacin (2017)
Rocha, Robson Silva; Valim, Ricardo Bertholo; Trevelin, Leandro Cesar; Silva, Fernando Lindo; Steter, Juliana Ribeiro; Zaiat, Marcelo; Lanza, Marcos Roberto de Vasconcelos
Source: Journal of Enviromental Chemical Engineering. Unidades: EESC, IQSC
Subjects: ELETRODO, REAÇÕES QUÍMICAS
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ABNT
ROCHA, Robson Silva et al. New operational mode of an electrochemical reactor and its application to the degradation of levofloxacin. Journal of Enviromental Chemical Engineering, v. 5, p. 4441-4446, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jece.2017.08.041. Acesso em: 12 ago. 2024.
APA
Rocha, R. S., Valim, R. B., Trevelin, L. C., Silva, F. L., Steter, J. R., Zaiat, M., & Lanza, M. R. de V. (2017). New operational mode of an electrochemical reactor and its application to the degradation of levofloxacin. Journal of Enviromental Chemical Engineering, 5, 4441-4446. doi:10.1016/j.jece.2017.08.041
NLM
Rocha RS, Valim RB, Trevelin LC, Silva FL, Steter JR, Zaiat M, Lanza MR de V. New operational mode of an electrochemical reactor and its application to the degradation of levofloxacin [Internet]. Journal of Enviromental Chemical Engineering. 2017 ; 5 4441-4446.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.jece.2017.08.041
Vancouver
Rocha RS, Valim RB, Trevelin LC, Silva FL, Steter JR, Zaiat M, Lanza MR de V. New operational mode of an electrochemical reactor and its application to the degradation of levofloxacin [Internet]. Journal of Enviromental Chemical Engineering. 2017 ; 5 4441-4446.[citado 2024 ago. 12 ] Available from: https://doi.org/10.1016/j.jece.2017.08.041

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