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Artigo de periodico
Diphenyl ditelluride assisted synthesis of noble metal-based silver-telluride 2D organometallic nanofibers with enhanced aggregation-induced emission (AIE) after oleylamine treatment (2023)
Djafari, Jamila; Duarte, Frederico; Lodeiro, Javier Fernández; Lodeiro, Adrián Fernández ; Santos, Hugo; Bladt, Eva; Bals, Sara; Savvidou, Aikaterini Flessa; Balicas, Luis; González, Benito Rodríguez; Santos, Alcindo Aparecido dos ; Martínez, José Luis Capelo; Lodeiro, Carlos
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: MATERIAIS NANOESTRUTURADOS, FLUORESCÊNCIA
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ABNT
DJAFARI, Jamila et al. Diphenyl ditelluride assisted synthesis of noble metal-based silver-telluride 2D organometallic nanofibers with enhanced aggregation-induced emission (AIE) after oleylamine treatment. Dyes and Pigments, v. 220, p. 1-6 art. 111754, 2023Tradução . . Disponível em: https://dx.doi.org/10.1016/j.dyepig.2023.111754. Acesso em: 05 jul. 2024.
APA
Djafari, J., Duarte, F., Lodeiro, J. F., Lodeiro, A. F., Santos, H., Bladt, E., et al. (2023). Diphenyl ditelluride assisted synthesis of noble metal-based silver-telluride 2D organometallic nanofibers with enhanced aggregation-induced emission (AIE) after oleylamine treatment. Dyes and Pigments, 220, 1-6 art. 111754. doi:10.1016/j.dyepig.2023.111754
NLM
Djafari J, Duarte F, Lodeiro JF, Lodeiro AF, Santos H, Bladt E, Bals S, Savvidou AF, Balicas L, González BR, Santos AA dos, Martínez JLC, Lodeiro C. Diphenyl ditelluride assisted synthesis of noble metal-based silver-telluride 2D organometallic nanofibers with enhanced aggregation-induced emission (AIE) after oleylamine treatment [Internet]. Dyes and Pigments. 2023 ; 220 1-6 art. 111754.[citado 2024 jul. 05 ] Available from: https://dx.doi.org/10.1016/j.dyepig.2023.111754
Vancouver
Djafari J, Duarte F, Lodeiro JF, Lodeiro AF, Santos H, Bladt E, Bals S, Savvidou AF, Balicas L, González BR, Santos AA dos, Martínez JLC, Lodeiro C. Diphenyl ditelluride assisted synthesis of noble metal-based silver-telluride 2D organometallic nanofibers with enhanced aggregation-induced emission (AIE) after oleylamine treatment [Internet]. Dyes and Pigments. 2023 ; 220 1-6 art. 111754.[citado 2024 jul. 05 ] Available from: https://dx.doi.org/10.1016/j.dyepig.2023.111754
Artigo de periodico
Ecofriendly synthesis of Zn-abietate complex derived from Pinus elliottii resin and its application as an antibacterial pigment against S. aureus and E. coli (2022)
Correa, Jamille S ; Primo, Júlia O ; Bittencourt, Carla ; Horsth, Dienifer F. L; Radovanovic, Eduardo; Toma, Henrique Eisi ; Zanette, Cristina M ; Anaissi, Fauze Jacó
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: ESCHERICHIA COLI, STAPHYLOCOCCUS, RESINAS, ESPECTROMETRIA DE MASSAS, PIGMENTOS
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CORREA, Jamille S et al. Ecofriendly synthesis of Zn-abietate complex derived from Pinus elliottii resin and its application as an antibacterial pigment against S. aureus and E. coli. Dyes and Pigments, v. 197, p. 1-9 art. 109946, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2021.109946. Acesso em: 05 jul. 2024.
APA
Correa, J. S., Primo, J. O., Bittencourt, C., Horsth, D. F. L., Radovanovic, E., Toma, H. E., et al. (2022). Ecofriendly synthesis of Zn-abietate complex derived from Pinus elliottii resin and its application as an antibacterial pigment against S. aureus and E. coli. Dyes and Pigments, 197, 1-9 art. 109946. doi:10.1016/j.dyepig.2021.109946
NLM
Correa JS, Primo JO, Bittencourt C, Horsth DFL, Radovanovic E, Toma HE, Zanette CM, Anaissi FJ. Ecofriendly synthesis of Zn-abietate complex derived from Pinus elliottii resin and its application as an antibacterial pigment against S. aureus and E. coli [Internet]. Dyes and Pigments. 2022 ; 197 1-9 art. 109946.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109946
Vancouver
Correa JS, Primo JO, Bittencourt C, Horsth DFL, Radovanovic E, Toma HE, Zanette CM, Anaissi FJ. Ecofriendly synthesis of Zn-abietate complex derived from Pinus elliottii resin and its application as an antibacterial pigment against S. aureus and E. coli [Internet]. Dyes and Pigments. 2022 ; 197 1-9 art. 109946.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109946
Artigo de periodico
Influence of electron-withdrawing groups in two-photon absorption of imidazopyridines derivatives (2022)
Pelosi, André Gasparotto; Cocca, Leandro Henrique Zucolotto; Abegão, Luis Miguel Gomes ; Sciuti, Lucas Fiocco ; Piguel, Sandrine; De Boni, Leonardo ; Mendonça, Cleber Renato
Fonte: Dyes and Pigments. Unidade: IFSC
Assuntos: FOTÔNICA, PROPRIEDADES DOS MATERIAIS, ÓPTICA NÃO LINEAR
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PELOSI, André Gasparotto et al. Influence of electron-withdrawing groups in two-photon absorption of imidazopyridines derivatives. Dyes and Pigments, v. 198, p. 109972-1-109972-7, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2021.109972. Acesso em: 05 jul. 2024.
APA
Pelosi, A. G., Cocca, L. H. Z., Abegão, L. M. G., Sciuti, L. F., Piguel, S., De Boni, L., & Mendonça, C. R. (2022). Influence of electron-withdrawing groups in two-photon absorption of imidazopyridines derivatives. Dyes and Pigments, 198, 109972-1-109972-7. doi:10.1016/j.dyepig.2021.109972
NLM
Pelosi AG, Cocca LHZ, Abegão LMG, Sciuti LF, Piguel S, De Boni L, Mendonça CR. Influence of electron-withdrawing groups in two-photon absorption of imidazopyridines derivatives [Internet]. Dyes and Pigments. 2022 ; 198 109972-1-109972-7.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109972
Vancouver
Pelosi AG, Cocca LHZ, Abegão LMG, Sciuti LF, Piguel S, De Boni L, Mendonça CR. Influence of electron-withdrawing groups in two-photon absorption of imidazopyridines derivatives [Internet]. Dyes and Pigments. 2022 ; 198 109972-1-109972-7.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109972
Artigo de periodico
Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding (2021)
Bertozo, Luiza Carvalho; Maszota-Zieleniak, Martyna; Bolean, Maytê ; Ciancaglini, Pietro ; Samsonov, Sergey A.; Ximenes, Valdecir Farias
Fonte: Dyes and Pigments. Unidade: FFCLRP
Assuntos: ALBUMINAS, FLUORESCÊNCIA, QUÍMICA FARMACÊUTICA, MODELAGEM MOLECULAR
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BERTOZO, Luiza Carvalho et al. Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding. Dyes and Pigments, v. 188, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2021.109195. Acesso em: 05 jul. 2024.
APA
Bertozo, L. C., Maszota-Zieleniak, M., Bolean, M., Ciancaglini, P., Samsonov, S. A., & Ximenes, V. F. (2021). Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding. Dyes and Pigments, 188. doi:10.1016/j.dyepig.2021.109195
NLM
Bertozo LC, Maszota-Zieleniak M, Bolean M, Ciancaglini P, Samsonov SA, Ximenes VF. Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding [Internet]. Dyes and Pigments. 2021 ; 188[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109195
Vancouver
Bertozo LC, Maszota-Zieleniak M, Bolean M, Ciancaglini P, Samsonov SA, Ximenes VF. Binding of fluorescent dansyl amino acids in albumin: when access to the protein cavity is more important than the strength of binding [Internet]. Dyes and Pigments. 2021 ; 188[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109195
Artigo de periodico
Color formulation in maxillofacial elastomer by genetic algorithm (2021)
Nakamura, Denise Moral ; Tessaro, Yargo Vo ; Furuie, Sérgio Shiguemi ; Coto, Neide Pena
Fonte: Dyes and Pigments. Unidades: FO, EP
Assuntos: ELASTÔMEROS, ALGORITMOS, PRÓTESE MAXILAR
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ABNT
NAKAMURA, Denise Moral et al. Color formulation in maxillofacial elastomer by genetic algorithm. Dyes and Pigments, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2021.109820. Acesso em: 05 jul. 2024.
APA
Nakamura, D. M., Tessaro, Y. V., Furuie, S. S., & Coto, N. P. (2021). Color formulation in maxillofacial elastomer by genetic algorithm. Dyes and Pigments. doi:10.1016/j.dyepig.2021.109820
NLM
Nakamura DM, Tessaro YV, Furuie SS, Coto NP. Color formulation in maxillofacial elastomer by genetic algorithm [Internet]. Dyes and Pigments. 2021 ;[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109820
Vancouver
Nakamura DM, Tessaro YV, Furuie SS, Coto NP. Color formulation in maxillofacial elastomer by genetic algorithm [Internet]. Dyes and Pigments. 2021 ;[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109820
Artigo de periodico
Alkylation of a hydrophilic photosensitizer enhances the contact-dependent photo-induced oxidation of phospholipid membranes (2021)
Vignoni, Alejandro ; Layana, Carla; Junqueira, Helena Couto; Thomas, Andrés H.; Itri, Rosangela ; Baptista, Maurício da Silva ; Vignoni, Mariana
Fonte: Dyes and Pigments. Unidades: IF, IQ
Assuntos: BIOFÍSICA, FÍSICO-QUÍMICA, MEMBRANAS CELULARES, FOTOSSENSIBILIZAÇÃO EM ANIMAL
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ABNT
VIGNONI, Alejandro et al. Alkylation of a hydrophilic photosensitizer enhances the contact-dependent photo-induced oxidation of phospholipid membranes. Dyes and Pigments, v. 187, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.109131. Acesso em: 05 jul. 2024.
APA
Vignoni, A., Layana, C., Junqueira, H. C., Thomas, A. H., Itri, R., Baptista, M. da S., & Vignoni, M. (2021). Alkylation of a hydrophilic photosensitizer enhances the contact-dependent photo-induced oxidation of phospholipid membranes. Dyes and Pigments, 187. doi:10.1016/j.dyepig.2020.109131
NLM
Vignoni A, Layana C, Junqueira HC, Thomas AH, Itri R, Baptista M da S, Vignoni M. Alkylation of a hydrophilic photosensitizer enhances the contact-dependent photo-induced oxidation of phospholipid membranes [Internet]. Dyes and Pigments. 2021 ; 187[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.109131
Vancouver
Vignoni A, Layana C, Junqueira HC, Thomas AH, Itri R, Baptista M da S, Vignoni M. Alkylation of a hydrophilic photosensitizer enhances the contact-dependent photo-induced oxidation of phospholipid membranes [Internet]. Dyes and Pigments. 2021 ; 187[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.109131
Artigo de periodico
Comparison of the effect of N-methyl and N-aryl groups on the hydrolytic stability and electronic properties of betalain dyes (2020)
Pioli, Renan Moraes ; Mattioli, Renan Rodini ; Esteves, Larissa Cerrato ; Dochev, Stefan; Bastos, Erick Leite
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: HIDRÓLISE, FLUORESCÊNCIA, PRODUTOS NATURAIS
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ABNT
PIOLI, Renan Moraes et al. Comparison of the effect of N-methyl and N-aryl groups on the hydrolytic stability and electronic properties of betalain dyes. Dyes and Pigments, v. 183, p. 1-7 art. 108609, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108609. Acesso em: 05 jul. 2024.
APA
Pioli, R. M., Mattioli, R. R., Esteves, L. C., Dochev, S., & Bastos, E. L. (2020). Comparison of the effect of N-methyl and N-aryl groups on the hydrolytic stability and electronic properties of betalain dyes. Dyes and Pigments, 183, 1-7 art. 108609. doi:10.1016/j.dyepig.2020.108609
NLM
Pioli RM, Mattioli RR, Esteves LC, Dochev S, Bastos EL. Comparison of the effect of N-methyl and N-aryl groups on the hydrolytic stability and electronic properties of betalain dyes [Internet]. Dyes and Pigments. 2020 ; 183 1-7 art. 108609.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108609
Vancouver
Pioli RM, Mattioli RR, Esteves LC, Dochev S, Bastos EL. Comparison of the effect of N-methyl and N-aryl groups on the hydrolytic stability and electronic properties of betalain dyes [Internet]. Dyes and Pigments. 2020 ; 183 1-7 art. 108609.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108609
Artigo de periodico
Self-aggregation of verteporfin in glioblastoma multiforme cells: a static and time-resolved fluorescence study (2020)
Calori, Italo Rodrigo ; Caetano, Wilker; Tedesco, Antônio Cláudio ; Hioka, Noboru
Fonte: Dyes and Pigments. Unidade: FFCLRP
Assuntos: PORFIRINAS, TERAPIA FOTODINÂMICA, FLUORESCÊNCIA
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ABNT
CALORI, Italo Rodrigo et al. Self-aggregation of verteporfin in glioblastoma multiforme cells: a static and time-resolved fluorescence study. Dyes and Pigments, v. 182, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108598. Acesso em: 05 jul. 2024.
APA
Calori, I. R., Caetano, W., Tedesco, A. C., & Hioka, N. (2020). Self-aggregation of verteporfin in glioblastoma multiforme cells: a static and time-resolved fluorescence study. Dyes and Pigments, 182. doi:10.1016/j.dyepig.2020.108598
NLM
Calori IR, Caetano W, Tedesco AC, Hioka N. Self-aggregation of verteporfin in glioblastoma multiforme cells: a static and time-resolved fluorescence study [Internet]. Dyes and Pigments. 2020 ; 182[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108598
Vancouver
Calori IR, Caetano W, Tedesco AC, Hioka N. Self-aggregation of verteporfin in glioblastoma multiforme cells: a static and time-resolved fluorescence study [Internet]. Dyes and Pigments. 2020 ; 182[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108598
Artigo de periodico
Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor (2020)
Paulino, Antonio Augusto Soares; Giroldo, Lilian; Pradie, Noriberto Araújo; Reis, Joel Savi dos; Back, Davi F; Braga, Ataualpa Albert Carmo ; Stefani, Hélio Alexandre ; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Fonte: Dyes and Pigments. Unidades: IQ, FCF
Assuntos: SELÊNIO, PALÁDIO, FLUORESCÊNCIA
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ABNT
PAULINO, Antonio Augusto Soares et al. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, v. 179, p. 1-10 art. 108355, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108355. Acesso em: 05 jul. 2024.
APA
Paulino, A. A. S., Giroldo, L., Pradie, N. A., Reis, J. S. dos, Back, D. F., Braga, A. A. C., et al. (2020). Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, 179, 1-10 art. 108355. doi:10.1016/j.dyepig.2020.108355
NLM
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Vancouver
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Artigo de periodico
Natural dye from Croton urucurana Baill. bark: Extraction, physicochemical characterization, textile dyeing and color fastness properties (2020)
Silva, Patrícia Muniz dos Santos; Fiaschitello, Ticiane Rossi; Queiroz, Rayana Santiago de; Freeman, Harold S; Costa, Silgia Aparecida da ; Leo, Patrícia; Montemor, Antonio Fernando; Costa, Sirlene Maria da
Fonte: Dyes and Pigments. Unidade: EACH
Assuntos: INDÚSTRIA TÊXTIL, CORANTES
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ABNT
SILVA, Patrícia Muniz dos Santos et al. Natural dye from Croton urucurana Baill. bark: Extraction, physicochemical characterization, textile dyeing and color fastness properties. Dyes and Pigments, v. 173, p. 01-14, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.107953. Acesso em: 05 jul. 2024.
APA
Silva, P. M. dos S., Fiaschitello, T. R., Queiroz, R. S. de, Freeman, H. S., Costa, S. A. da, Leo, P., et al. (2020). Natural dye from Croton urucurana Baill. bark: Extraction, physicochemical characterization, textile dyeing and color fastness properties. Dyes and Pigments, 173, 01-14. doi:10.1016/j.dyepig.2019.107953
NLM
Silva PM dos S, Fiaschitello TR, Queiroz RS de, Freeman HS, Costa SA da, Leo P, Montemor AF, Costa SM da. Natural dye from Croton urucurana Baill. bark: Extraction, physicochemical characterization, textile dyeing and color fastness properties [Internet]. Dyes and Pigments. 2020 ; 173 01-14.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107953
Vancouver
Silva PM dos S, Fiaschitello TR, Queiroz RS de, Freeman HS, Costa SA da, Leo P, Montemor AF, Costa SM da. Natural dye from Croton urucurana Baill. bark: Extraction, physicochemical characterization, textile dyeing and color fastness properties [Internet]. Dyes and Pigments. 2020 ; 173 01-14.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107953
Artigo de periodico
Nitrosation of BODIPY dyes and their applications in the development of thiol sensors (2020)
Melo, Shaiani Maria Gil de; Rezende, Lucas Cunha Dias de; Petrilli, Raquel ; Lopez, Renata Fonseca Vianna ; Goulart, Marilia O. F.; Emery, Flavio da Silva
Fonte: Dyes and Pigments. Unidade: FCFRP
Assuntos: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS, SENSORES QUÍMICOS, CORANTES FLUORESCENTES
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ABNT
MELO, Shaiani Maria Gil de et al. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors. Dyes and Pigments, v. 173, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.107885. Acesso em: 05 jul. 2024.
APA
Melo, S. M. G. de, Rezende, L. C. D. de, Petrilli, R., Lopez, R. F. V., Goulart, M. O. F., & Emery, F. da S. (2020). Nitrosation of BODIPY dyes and their applications in the development of thiol sensors. Dyes and Pigments, 173, 1-7. doi:10.1016/j.dyepig.2019.107885
NLM
Melo SMG de, Rezende LCD de, Petrilli R, Lopez RFV, Goulart MOF, Emery F da S. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors [Internet]. Dyes and Pigments. 2020 ; 173 1-7.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107885
Vancouver
Melo SMG de, Rezende LCD de, Petrilli R, Lopez RFV, Goulart MOF, Emery F da S. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors [Internet]. Dyes and Pigments. 2020 ; 173 1-7.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107885
Artigo de periodico
Aluminum chloride phthalocyanine in MCF-7: Rationally accounting for state of aggregation of photosensitizers inside cells (2020)
Calori, Italo Rodrigo ; Tedesco, Antônio Cláudio
Fonte: Dyes and Pigments. Unidade: FFCLRP
Assuntos: FITOTERAPIA, NANOTECNOLOGIA, NEOPLASIAS
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ABNT
CALORI, Italo Rodrigo e TEDESCO, Antônio Cláudio. Aluminum chloride phthalocyanine in MCF-7: Rationally accounting for state of aggregation of photosensitizers inside cells. Dyes and Pigments, v. 173, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.107940. Acesso em: 05 jul. 2024.
APA
Calori, I. R., & Tedesco, A. C. (2020). Aluminum chloride phthalocyanine in MCF-7: Rationally accounting for state of aggregation of photosensitizers inside cells. Dyes and Pigments, 173. doi:10.1016/j.dyepig.2019.107940
NLM
Calori IR, Tedesco AC. Aluminum chloride phthalocyanine in MCF-7: Rationally accounting for state of aggregation of photosensitizers inside cells [Internet]. Dyes and Pigments. 2020 ; 173[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107940
Vancouver
Calori IR, Tedesco AC. Aluminum chloride phthalocyanine in MCF-7: Rationally accounting for state of aggregation of photosensitizers inside cells [Internet]. Dyes and Pigments. 2020 ; 173[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107940
Artigo de periodico
Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation (2020)
Amorim, Vanessa G.; Melo, Shaiani Maria Gil de; Leite, Ruan F.; Coutinho, Paulo Arthur; Silva, Sarah M. P. da; Silva, André R.; Amorim, Fernanda G.; Pires, Rita G. W.; Coitinho, Juliana B.; Emery, Flavio da Silva ; Rezende, Lucas C. D.
Fonte: Dyes and Pigments. Unidade: FCFRP
Assuntos: PROTEÍNAS, FLUORESCÊNCIA, CORANTES FLUORESCENTES, BIOQUÍMICA, BIOTECNOLOGIA
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ABNT
AMORIM, Vanessa G. et al. Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation. Dyes and Pigments, v. 182, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108646. Acesso em: 05 jul. 2024.
APA
Amorim, V. G., Melo, S. M. G. de, Leite, R. F., Coutinho, P. A., Silva, S. M. P. da, Silva, A. R., et al. (2020). Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation. Dyes and Pigments, 182, 1-7. doi:10.1016/j.dyepig.2020.108646
NLM
Amorim VG, Melo SMG de, Leite RF, Coutinho PA, Silva SMP da, Silva AR, Amorim FG, Pires RGW, Coitinho JB, Emery F da S, Rezende LCD. Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation [Internet]. Dyes and Pigments. 2020 ; 182 1-7.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108646
Vancouver
Amorim VG, Melo SMG de, Leite RF, Coutinho PA, Silva SMP da, Silva AR, Amorim FG, Pires RGW, Coitinho JB, Emery F da S, Rezende LCD. Synthesis and characterization of two novel red-shifted isothiocyanate BODIPYs and their application in protein conjugation [Internet]. Dyes and Pigments. 2020 ; 182 1-7.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108646
Artigo de periodico
Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution (2019)
Santos, Fabiano S; Zanotto, Gabriel M; Argomedo, Luiz M. Z; Darbem, Mariana P; Gonçalves, Paulo F. B; Stefani, Hélio Alexandre ; Rodembusch, Fabiano S
Fonte: Dyes and Pigments. Unidade: FCF
Assuntos: SENSORES ÓPTICOS, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Fabiano S et al. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, v. 165, p. 372-382, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.02.047. Acesso em: 05 jul. 2024.
APA
Santos, F. S., Zanotto, G. M., Argomedo, L. M. Z., Darbem, M. P., Gonçalves, P. F. B., Stefani, H. A., & Rodembusch, F. S. (2019). Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, 165, 372-382. doi:10.1016/j.dyepig.2019.02.047
NLM
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
Vancouver
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
Artigo de periodico
Oxidation of tellurium dyes induced by mercury: more insights on the naked-eye and fluorescent Hg2+ detection (2019)
Paulino, Antônio A. Soares; Giroldo, Lilian; Celante, Gizele; Oliveira, Elisabete; Santos, Sérgio M; Mendes, Ricardo F; Paz, Filipe A. Almeida; Fioroto, Alexandre Minami; Oliveira, Pedro Vitoriano de ; Serrano, Silvia Helena Pires ; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: OXIDAÇÃO, TELÚRIO, MERCÚRIO (ELEMENTO QUÍMICO)
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ABNT
PAULINO, Antônio A. Soares et al. Oxidation of tellurium dyes induced by mercury: more insights on the naked-eye and fluorescent Hg2+ detection. Dyes and Pigments, v. 160, p. 208-216, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2018.07.055. Acesso em: 05 jul. 2024.
APA
Paulino, A. A. S., Giroldo, L., Celante, G., Oliveira, E., Santos, S. M., Mendes, R. F., et al. (2019). Oxidation of tellurium dyes induced by mercury: more insights on the naked-eye and fluorescent Hg2+ detection. Dyes and Pigments, 160, 208-216. doi:10.1016/j.dyepig.2018.07.055
NLM
Paulino AAS, Giroldo L, Celante G, Oliveira E, Santos SM, Mendes RF, Paz FAA, Fioroto AM, Oliveira PV de, Serrano SHP, Lodeiro C, Santos AA dos. Oxidation of tellurium dyes induced by mercury: more insights on the naked-eye and fluorescent Hg2+ detection [Internet]. Dyes and Pigments. 2019 ; 160 208-216.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.07.055
Vancouver
Paulino AAS, Giroldo L, Celante G, Oliveira E, Santos SM, Mendes RF, Paz FAA, Fioroto AM, Oliveira PV de, Serrano SHP, Lodeiro C, Santos AA dos. Oxidation of tellurium dyes induced by mercury: more insights on the naked-eye and fluorescent Hg2+ detection [Internet]. Dyes and Pigments. 2019 ; 160 208-216.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.07.055
Artigo de periodico
Formation of an emissive telluroxide promoted by `Hg POT. 2´+ in aqueous environment: a new naked-eye and ratiometric rhodamine dimer fluorescent mercury(II) probe (2018)
Paulino, Antônio A. Soares; Giroldo, Lilian; Celante, Gizele; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: TELÚRIO, MERCÚRIO (ELEMENTO QUÍMICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULINO, Antônio A. Soares et al. Formation of an emissive telluroxide promoted by `Hg POT. 2´+ in aqueous environment: a new naked-eye and ratiometric rhodamine dimer fluorescent mercury(II) probe. Dyes and Pigments, v. 159, p. 121-127, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2018.06.005. Acesso em: 05 jul. 2024.
APA
Paulino, A. A. S., Giroldo, L., Celante, G., Lodeiro, C., & Santos, A. A. dos. (2018). Formation of an emissive telluroxide promoted by `Hg POT. 2´+ in aqueous environment: a new naked-eye and ratiometric rhodamine dimer fluorescent mercury(II) probe. Dyes and Pigments, 159, 121-127. doi:10.1016/j.dyepig.2018.06.005
NLM
Paulino AAS, Giroldo L, Celante G, Lodeiro C, Santos AA dos. Formation of an emissive telluroxide promoted by `Hg POT. 2´+ in aqueous environment: a new naked-eye and ratiometric rhodamine dimer fluorescent mercury(II) probe [Internet]. Dyes and Pigments. 2018 ; 159 121-127.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.06.005
Vancouver
Paulino AAS, Giroldo L, Celante G, Lodeiro C, Santos AA dos. Formation of an emissive telluroxide promoted by `Hg POT. 2´+ in aqueous environment: a new naked-eye and ratiometric rhodamine dimer fluorescent mercury(II) probe [Internet]. Dyes and Pigments. 2018 ; 159 121-127.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.06.005
Artigo de periodico
Bioinspired water-soluble two-photon fluorophores (2018)
Rodrigues, Ana Clara Beltran; Mariz, Inês de Fátima Afonso; Maçoas, Ermelinda Maria Sengo; Tonelli, Renata Rosito; Martinho, José Manuel Gaspar; Quina, Frank Herbert ; Bastos, Erick Leite
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: PIGMENTOS VEGETAIS, FLUORESCÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRIGUES, Ana Clara Beltran et al. Bioinspired water-soluble two-photon fluorophores. Dyes and Pigments, v. 150, p. 105-111, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2017.11.020. Acesso em: 05 jul. 2024.
APA
Rodrigues, A. C. B., Mariz, I. de F. A., Maçoas, E. M. S., Tonelli, R. R., Martinho, J. M. G., Quina, F. H., & Bastos, E. L. (2018). Bioinspired water-soluble two-photon fluorophores. Dyes and Pigments, 150, 105-111. doi:10.1016/j.dyepig.2017.11.020
NLM
Rodrigues ACB, Mariz I de FA, Maçoas EMS, Tonelli RR, Martinho JMG, Quina FH, Bastos EL. Bioinspired water-soluble two-photon fluorophores [Internet]. Dyes and Pigments. 2018 ; 150 105-111.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2017.11.020
Vancouver
Rodrigues ACB, Mariz I de FA, Maçoas EMS, Tonelli RR, Martinho JMG, Quina FH, Bastos EL. Bioinspired water-soluble two-photon fluorophores [Internet]. Dyes and Pigments. 2018 ; 150 105-111.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2017.11.020
Artigo de periodico
New emissive mononuclear copper (I) complex: structural and photophysical characterization focusing on solvatochromism, rigidochromism and oxygen sensing in mesoporous solid matrix (2018)
Ravaro, Leandro P.; Mafud, Ana C.; Li, Zhi; Reinheimer, Eric W.; Simone, Carlos A.; Mascarenhas, Yvonne Primerano; Ford, Peter C.; de Camargo, Andrea Simone Stucchi
Fonte: Dyes and Pigments. Unidade: IFSC
Assuntos: FOTOLUMINESCÊNCIA, VIDROS METÁLICOS
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ABNT
RAVARO, Leandro P. et al. New emissive mononuclear copper (I) complex: structural and photophysical characterization focusing on solvatochromism, rigidochromism and oxygen sensing in mesoporous solid matrix. Dyes and Pigments, v. 159, p. 464-470, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2018.07.020. Acesso em: 05 jul. 2024.
APA
Ravaro, L. P., Mafud, A. C., Li, Z., Reinheimer, E. W., Simone, C. A., Mascarenhas, Y. P., et al. (2018). New emissive mononuclear copper (I) complex: structural and photophysical characterization focusing on solvatochromism, rigidochromism and oxygen sensing in mesoporous solid matrix. Dyes and Pigments, 159, 464-470. doi:10.1016/j.dyepig.2018.07.020
NLM
Ravaro LP, Mafud AC, Li Z, Reinheimer EW, Simone CA, Mascarenhas YP, Ford PC, de Camargo ASS. New emissive mononuclear copper (I) complex: structural and photophysical characterization focusing on solvatochromism, rigidochromism and oxygen sensing in mesoporous solid matrix [Internet]. Dyes and Pigments. 2018 ; 159 464-470.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.07.020
Vancouver
Ravaro LP, Mafud AC, Li Z, Reinheimer EW, Simone CA, Mascarenhas YP, Ford PC, de Camargo ASS. New emissive mononuclear copper (I) complex: structural and photophysical characterization focusing on solvatochromism, rigidochromism and oxygen sensing in mesoporous solid matrix [Internet]. Dyes and Pigments. 2018 ; 159 464-470.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.07.020
Artigo de periodico
Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors (2018)
Rezende, Lucas C. D.; Melo, Shaiani M. G.; Boodts, Stijn; Verbelen, Bram; Emery, Flavio da Silva; Dehaen, Wim
Fonte: Dyes and Pigments. Unidade: FCFRP
Assuntos: CORANTES FLUORESCENTES, RESSONÂNCIA MAGNÉTICA NUCLEAR, SENSORES QUÍMICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REZENDE, Lucas C. D. et al. Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors. Dyes and Pigments, v. 154, p. 155-163, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2018.01.043. Acesso em: 05 jul. 2024.
APA
Rezende, L. C. D., Melo, S. M. G., Boodts, S., Verbelen, B., Emery, F. da S., & Dehaen, W. (2018). Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors. Dyes and Pigments, 154, 155-163. doi:10.1016/j.dyepig.2018.01.043
NLM
Rezende LCD, Melo SMG, Boodts S, Verbelen B, Emery F da S, Dehaen W. Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors [Internet]. Dyes and Pigments. 2018 ; 154 155-163.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.01.043
Vancouver
Rezende LCD, Melo SMG, Boodts S, Verbelen B, Emery F da S, Dehaen W. Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors [Internet]. Dyes and Pigments. 2018 ; 154 155-163.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2018.01.043
Artigo de periodico
Chlorin derivatives sterically-prevented from self-aggregation with high antitumor activity for photodynamic therapy (2017)
Linares, Irwin A P; Oliveira, Kleber Thiago de; Perussi, Janice Rodrigues
Fonte: Dyes and Pigments. Unidade: IQSC
Assuntos: CLORO, BIOQUÍMICA CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LINARES, Irwin A P e OLIVEIRA, Kleber Thiago de e PERUSSI, Janice Rodrigues. Chlorin derivatives sterically-prevented from self-aggregation with high antitumor activity for photodynamic therapy. Dyes and Pigments, v. 145, p. 518-527, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2017.06.011. Acesso em: 05 jul. 2024.
APA
Linares, I. A. P., Oliveira, K. T. de, & Perussi, J. R. (2017). Chlorin derivatives sterically-prevented from self-aggregation with high antitumor activity for photodynamic therapy. Dyes and Pigments, 145, 518-527. doi:10.1016/j.dyepig.2017.06.011
NLM
Linares IAP, Oliveira KT de, Perussi JR. Chlorin derivatives sterically-prevented from self-aggregation with high antitumor activity for photodynamic therapy [Internet]. Dyes and Pigments. 2017 ; 145 518-527.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2017.06.011
Vancouver
Linares IAP, Oliveira KT de, Perussi JR. Chlorin derivatives sterically-prevented from self-aggregation with high antitumor activity for photodynamic therapy [Internet]. Dyes and Pigments. 2017 ; 145 518-527.[citado 2024 jul. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2017.06.011

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