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Artigo de periodico
1,1-Difluoro-1,3,5,2-triazaborinines containing benzo-fused imidazo-, oxazolo-, and thiazolo-pyrimido as a new luminescent framework (2024)
Cassol, Ricardo R.C.; Luz, Fábio M.; Machado, Érica T.O.; Pereira, Victor S.; Frizzo, Clarissa P.; Martins, Marcos A.P.; Zanatta, Nilo; Deflon, Victor Marcelo ; Cunha, Rafaela C.; Iglesias, Bernardo A.; Bonacorso, Helio G.
Fonte: Dyes and Pigments. Unidade: IQSC
Assuntos: FLUORESCÊNCIA, SÍNTESE QUÍMICA
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ABNT
CASSOL, Ricardo R.C. et al. 1,1-Difluoro-1,3,5,2-triazaborinines containing benzo-fused imidazo-, oxazolo-, and thiazolo-pyrimido as a new luminescent framework. Dyes and Pigments, v. 231, p. 112435, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2024.112435. Acesso em: 05 out. 2024.
APA
Cassol, R. R. C., Luz, F. M., Machado, É. T. O., Pereira, V. S., Frizzo, C. P., Martins, M. A. P., et al. (2024). 1,1-Difluoro-1,3,5,2-triazaborinines containing benzo-fused imidazo-, oxazolo-, and thiazolo-pyrimido as a new luminescent framework. Dyes and Pigments, 231, 112435. doi:10.1016/j.dyepig.2024.112435
NLM
Cassol RRC, Luz FM, Machado ÉTO, Pereira VS, Frizzo CP, Martins MAP, Zanatta N, Deflon VM, Cunha RC, Iglesias BA, Bonacorso HG. 1,1-Difluoro-1,3,5,2-triazaborinines containing benzo-fused imidazo-, oxazolo-, and thiazolo-pyrimido as a new luminescent framework [Internet]. Dyes and Pigments. 2024 ;231 112435.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2024.112435
Vancouver
Cassol RRC, Luz FM, Machado ÉTO, Pereira VS, Frizzo CP, Martins MAP, Zanatta N, Deflon VM, Cunha RC, Iglesias BA, Bonacorso HG. 1,1-Difluoro-1,3,5,2-triazaborinines containing benzo-fused imidazo-, oxazolo-, and thiazolo-pyrimido as a new luminescent framework [Internet]. Dyes and Pigments. 2024 ;231 112435.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2024.112435
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 out. 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 out. 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 out. 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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ABNT
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 out. 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 out. 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 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109946
Artigo de periodico
Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines (2022)
Bertallo, Camila Rodrigues de Souza ; Berlim, Leonardo S.; Olivier, Danilo S.; Arroio, Thais Rodrigues ; Ito, Amando Siuiti ; Clososki, Giuliano Cesar
Fonte: Dyes and Pigments. Unidades: FFCLRP, FCFRP
Assuntos: FÍSICO-QUÍMICA, COMPOSIÇÃO QUÍMICA
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ABNT
BERTALLO, Camila Rodrigues de Souza et al. Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines. Dyes and Pigments, v. 198, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2021.109996. Acesso em: 05 out. 2024.
APA
Bertallo, C. R. de S., Berlim, L. S., Olivier, D. S., Arroio, T. R., Ito, A. S., & Clososki, G. C. (2022). Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines. Dyes and Pigments, 198. doi:10.1016/j.dyepig.2021.109996
NLM
Bertallo CR de S, Berlim LS, Olivier DS, Arroio TR, Ito AS, Clososki GC. Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines [Internet]. Dyes and Pigments. 2022 ; 198[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109996
Vancouver
Bertallo CR de S, Berlim LS, Olivier DS, Arroio TR, Ito AS, Clososki GC. Synthesis and photophysical properties of 2-aryl-5-carbonyl indolizines [Internet]. Dyes and Pigments. 2022 ; 198[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109996
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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ABNT
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 out. 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 out. 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 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109972
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 out. 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 out. 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 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109820
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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ABNT
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 out. 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 out. 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 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109195
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 out. 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 out. 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 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2020.109131
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
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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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 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)
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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 out. 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 out. 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 out. 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
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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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 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 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2017.06.011
Artigo de periodico
The confidence of blue: a new highly selective bio-inspired coumarin emissive probe for fluoride recognition (2016)
Gonçalves, Augusto Cesar; Sato, Nayara C; Santos, Hugo M; Capelo, José Luis; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Fonte: Dyes and Pigments. Unidade: IQ
Assunto: FLUORESCÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GONÇALVES, Augusto Cesar et al. The confidence of blue: a new highly selective bio-inspired coumarin emissive probe for fluoride recognition. Dyes and Pigments, v. 135, p. 177-183, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2016.02.032. Acesso em: 05 out. 2024.
APA
Gonçalves, A. C., Sato, N. C., Santos, H. M., Capelo, J. L., Lodeiro, C., & Santos, A. A. dos. (2016). The confidence of blue: a new highly selective bio-inspired coumarin emissive probe for fluoride recognition. Dyes and Pigments, 135, 177-183. doi:10.1016/j.dyepig.2016.02.032
NLM
Gonçalves AC, Sato NC, Santos HM, Capelo JL, Lodeiro C, Santos AA dos. The confidence of blue: a new highly selective bio-inspired coumarin emissive probe for fluoride recognition [Internet]. Dyes and Pigments. 2016 ; 135 177-183.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2016.02.032
Vancouver
Gonçalves AC, Sato NC, Santos HM, Capelo JL, Lodeiro C, Santos AA dos. The confidence of blue: a new highly selective bio-inspired coumarin emissive probe for fluoride recognition [Internet]. Dyes and Pigments. 2016 ; 135 177-183.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2016.02.032
Artigo de periodico
Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures (2015)
Santin, Luiza R. R; Santos, Sandra Carvalho dos; Novo, Diogo La Rosa; Bianchini, Daniela; Gerola, Adriana P; Braga, Gustavo; Caetano, Wilker; Moreira, Leonardo M; Bastos, Erick Leite ; Romani, Ana Paula; Oliveira, Hueder P. M. de
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: FLUORESCÊNCIA, SOLVENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTIN, Luiza R. R et al. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures. Dyes and Pigments, v. 119, p. 12-21, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2015.03.004. Acesso em: 05 out. 2024.
APA
Santin, L. R. R., Santos, S. C. dos, Novo, D. L. R., Bianchini, D., Gerola, A. P., Braga, G., et al. (2015). Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures. Dyes and Pigments, 119, 12-21. doi:10.1016/j.dyepig.2015.03.004
NLM
Santin LRR, Santos SC dos, Novo DLR, Bianchini D, Gerola AP, Braga G, Caetano W, Moreira LM, Bastos EL, Romani AP, Oliveira HPM de. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures [Internet]. Dyes and Pigments. 2015 ; 119 12-21.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
Vancouver
Santin LRR, Santos SC dos, Novo DLR, Bianchini D, Gerola AP, Braga G, Caetano W, Moreira LM, Bastos EL, Romani AP, Oliveira HPM de. Study between solvatochromism and steady-state and time-resolved fluorescence measurements of the Methylene blue in binary mixtures [Internet]. Dyes and Pigments. 2015 ; 119 12-21.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
Artigo de periodico
Preparation, characterization, and in vitro phototoxic effect of zinc phthalocyanine cucurbit[7]uril complex encapsulated into liposomes (2014)
Bolfarini, Gisele C.; Siqueira-Moura, Marigilson P.; Demets, Grégoire Jean-François; Tedesco, Antonio Claudio
Fonte: Dyes and Pigments. Unidade: FFCLRP
Assuntos: LIPOSSOMOS, MELANOMA, TERAPIA FOTODINÂMICA, ENGENHARIA TECIDUAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BOLFARINI, Gisele C. et al. Preparation, characterization, and in vitro phototoxic effect of zinc phthalocyanine cucurbit[7]uril complex encapsulated into liposomes. Dyes and Pigments, v. 100, p. 162-167, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.08.018. Acesso em: 05 out. 2024.
APA
Bolfarini, G. C., Siqueira-Moura, M. P., Demets, G. J. -F., & Tedesco, A. C. (2014). Preparation, characterization, and in vitro phototoxic effect of zinc phthalocyanine cucurbit[7]uril complex encapsulated into liposomes. Dyes and Pigments, 100, 162-167. doi:10.1016/j.dyepig.2013.08.018
NLM
Bolfarini GC, Siqueira-Moura MP, Demets GJ-F, Tedesco AC. Preparation, characterization, and in vitro phototoxic effect of zinc phthalocyanine cucurbit[7]uril complex encapsulated into liposomes [Internet]. Dyes and Pigments. 2014 ; 100 162-167.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2013.08.018
Vancouver
Bolfarini GC, Siqueira-Moura MP, Demets GJ-F, Tedesco AC. Preparation, characterization, and in vitro phototoxic effect of zinc phthalocyanine cucurbit[7]uril complex encapsulated into liposomes [Internet]. Dyes and Pigments. 2014 ; 100 162-167.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2013.08.018
Artigo de periodico
New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices (2014)
Núñez, Cristina; Diniz, Mário; Santos, Alcindo Aparecido dos ; Capelo, José Luis; Lodeiro, Carlos
Fonte: Dyes and Pigments. Unidade: IQ
Assuntos: FLUORESCÊNCIA, MERCÚRIO (ELEMENTO QUÍMICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NÚÑEZ, Cristina et al. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices. Dyes and Pigments, v. 101, p. 156-163, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.09.019. Acesso em: 05 out. 2024.
APA
Núñez, C., Diniz, M., Santos, A. A. dos, Capelo, J. L., & Lodeiro, C. (2014). New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices. Dyes and Pigments, 101, 156-163. doi:10.1016/j.dyepig.2013.09.019
NLM
Núñez C, Diniz M, Santos AA dos, Capelo JL, Lodeiro C. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices [Internet]. Dyes and Pigments. 2014 ; 101 156-163.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2013.09.019
Vancouver
Núñez C, Diniz M, Santos AA dos, Capelo JL, Lodeiro C. New rhodamine dimer probes for mercury detection via color changes and enhancement of the fluorescence emission: Fast recognition in cellulose supported devices [Internet]. Dyes and Pigments. 2014 ; 101 156-163.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2013.09.019
Artigo de periodico
Investigation of ground and excited state photophysical properties of gadolinium phthalocyanine (2014)
Vivas, Marcelo G.; De Boni, Leonardo ; Gaffo, Luciana; Mendonça, Cleber Renato
Fonte: Dyes and Pigments. Unidade: IFSC
Assuntos: FLUORESCÊNCIA, ABSORÇÃO DA LUZ, FOTÔNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIVAS, Marcelo G. et al. Investigation of ground and excited state photophysical properties of gadolinium phthalocyanine. Dyes and Pigments, v. 101, p. 338-343, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.10.026. Acesso em: 05 out. 2024.
APA
Vivas, M. G., De Boni, L., Gaffo, L., & Mendonça, C. R. (2014). Investigation of ground and excited state photophysical properties of gadolinium phthalocyanine. Dyes and Pigments, 101, 338-343. doi:10.1016/j.dyepig.2013.10.026
NLM
Vivas MG, De Boni L, Gaffo L, Mendonça CR. Investigation of ground and excited state photophysical properties of gadolinium phthalocyanine [Internet]. Dyes and Pigments. 2014 ; 101 338-343.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2013.10.026
Vancouver
Vivas MG, De Boni L, Gaffo L, Mendonça CR. Investigation of ground and excited state photophysical properties of gadolinium phthalocyanine [Internet]. Dyes and Pigments. 2014 ; 101 338-343.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.dyepig.2013.10.026

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