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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: 25 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. 25 ] 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. 25 ] 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: 25 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. 25 ] 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. 25 ] 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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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: 25 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. 25 ] 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. 25 ] 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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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: 25 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. 25 ] 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. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2020.109131
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: 25 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. 25 ] 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. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108598
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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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: 25 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. 25 ] 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. 25 ] 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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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: 25 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. 25 ] 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. 25 ] 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: 25 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. 25 ] 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. 25 ] 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: 25 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. 25 ] 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. 25 ] 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
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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: 25 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. 25 ] 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. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
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: 25 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. 25 ] 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. 25 ] 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
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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: 25 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. 25 ] 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. 25 ] 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
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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: 25 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. 25 ] 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. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2017.06.011
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
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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: 25 jul. 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 jul. 25 ] 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 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2013.08.018
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: 25 jul. 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 jul. 25 ] 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 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2013.10.026
Artigo de periodico
Synthesis of functionalized chlorins sterically-prevented from self-aggregation (2013)
Santos, Fabiane A. B. dos; Uchoa, Adjaci Fernandes; Baptista, Maurício da Silva ; Iamamoto, Yassuko; Serra, Osvaldo Antonio; Brocksom, Timothy John; Oliveira, Kleber Thiago de
Fonte: Dyes and Pigments. Unidades: IQ, FFCLRP
Assunto: FOTOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Fabiane A. B. dos et al. Synthesis of functionalized chlorins sterically-prevented from self-aggregation. Dyes and Pigments, v. 99, n. 2, p. 402-411, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.05.024. Acesso em: 25 jul. 2024.
APA
Santos, F. A. B. dos, Uchoa, A. F., Baptista, M. da S., Iamamoto, Y., Serra, O. A., Brocksom, T. J., & Oliveira, K. T. de. (2013). Synthesis of functionalized chlorins sterically-prevented from self-aggregation. Dyes and Pigments, 99( 2), 402-411. doi:10.1016/j.dyepig.2013.05.024
NLM
Santos FAB dos, Uchoa AF, Baptista M da S, Iamamoto Y, Serra OA, Brocksom TJ, Oliveira KT de. Synthesis of functionalized chlorins sterically-prevented from self-aggregation [Internet]. Dyes and Pigments. 2013 ; 99( 2): 402-411.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
Vancouver
Santos FAB dos, Uchoa AF, Baptista M da S, Iamamoto Y, Serra OA, Brocksom TJ, Oliveira KT de. Synthesis of functionalized chlorins sterically-prevented from self-aggregation [Internet]. Dyes and Pigments. 2013 ; 99( 2): 402-411.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
Artigo de periodico
Cerium phosphate nanoparticles with low photocatalytic activity for UV light absorption application in photoprotection (2013)
Lima, Juliana Fonseca de; Serra, Osvaldo Antonio
Fonte: Dyes and Pigments. Unidade: FFCLRP
Assuntos: CÉRIO, NANOPARTÍCULAS, TERRAS RARAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Juliana Fonseca de e SERRA, Osvaldo Antonio. Cerium phosphate nanoparticles with low photocatalytic activity for UV light absorption application in photoprotection. Dyes and Pigments, v. 97, n. 2, p. 291-296, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2012.12.020. Acesso em: 25 jul. 2024.
APA
Lima, J. F. de, & Serra, O. A. (2013). Cerium phosphate nanoparticles with low photocatalytic activity for UV light absorption application in photoprotection. Dyes and Pigments, 97( 2), 291-296. doi:10.1016/j.dyepig.2012.12.020
NLM
Lima JF de, Serra OA. Cerium phosphate nanoparticles with low photocatalytic activity for UV light absorption application in photoprotection [Internet]. Dyes and Pigments. 2013 ; 97( 2): 291-296.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2012.12.020
Vancouver
Lima JF de, Serra OA. Cerium phosphate nanoparticles with low photocatalytic activity for UV light absorption application in photoprotection [Internet]. Dyes and Pigments. 2013 ; 97( 2): 291-296.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2012.12.020
Artigo de periodico
Synthesis of functionalized chlorins sterically-prevented from self-aggregation (2013)
Santos, Fabiane A. B. dos; Uchoa, Adjaci F.; Baptista, Maurício da Silva ; Iamamoto, Yassuko; Serra, Osvaldo Antonio; Brocksom, Timothy J.; Oliveira, Kleber T. de
Fonte: Dyes and Pigments. Unidades: IQ, FFCLRP
Assuntos: QUÍMICA INORGÂNICA, SÍNTESE INORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Fabiane A. B. dos et al. Synthesis of functionalized chlorins sterically-prevented from self-aggregation. Dyes and Pigments, v. 99, n. 2, p. 402-411, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2013.05.024. Acesso em: 25 jul. 2024.
APA
Santos, F. A. B. dos, Uchoa, A. F., Baptista, M. da S., Iamamoto, Y., Serra, O. A., Brocksom, T. J., & Oliveira, K. T. de. (2013). Synthesis of functionalized chlorins sterically-prevented from self-aggregation. Dyes and Pigments, 99( 2), 402-411. doi:10.1016/j.dyepig.2013.05.024
NLM
Santos FAB dos, Uchoa AF, Baptista M da S, Iamamoto Y, Serra OA, Brocksom TJ, Oliveira KT de. Synthesis of functionalized chlorins sterically-prevented from self-aggregation [Internet]. Dyes and Pigments. 2013 ; 99( 2): 402-411.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
Vancouver
Santos FAB dos, Uchoa AF, Baptista M da S, Iamamoto Y, Serra OA, Brocksom TJ, Oliveira KT de. Synthesis of functionalized chlorins sterically-prevented from self-aggregation [Internet]. Dyes and Pigments. 2013 ; 99( 2): 402-411.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
Artigo de periodico
New porphyrins tailored as biodiesel fluorescent markers (2011)
Figueira, Ana Cecília B.; Oliveira, Kleber T.; Serra, Osvaldo Antonio
Fonte: Dyes and Pigments. Unidade: FFCLRP
Assuntos: BIODIESEL, FLUORESCÊNCIA, ESPECTROSCOPIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIGUEIRA, Ana Cecília B. e OLIVEIRA, Kleber T. e SERRA, Osvaldo Antonio. New porphyrins tailored as biodiesel fluorescent markers. Dyes and Pigments, v. 1, n. 3, p. 383-388, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2011.05.020. Acesso em: 25 jul. 2024.
APA
Figueira, A. C. B., Oliveira, K. T., & Serra, O. A. (2011). New porphyrins tailored as biodiesel fluorescent markers. Dyes and Pigments, 1( 3), 383-388. doi:10.1016/j.dyepig.2011.05.020
NLM
Figueira ACB, Oliveira KT, Serra OA. New porphyrins tailored as biodiesel fluorescent markers [Internet]. Dyes and Pigments. 2011 ; 1( 3): 383-388.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2011.05.020
Vancouver
Figueira ACB, Oliveira KT, Serra OA. New porphyrins tailored as biodiesel fluorescent markers [Internet]. Dyes and Pigments. 2011 ; 1( 3): 383-388.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2011.05.020
Artigo de periodico
Colored films produced by electron beam deposition from nanometric Ti'O IND. 2' and 'Al IND. 2''O IND. 3' pigment powders obtained by modified polymeric precursor method (2007)
Bernardi, Maria Inês Basso; De Vicente, Fábio Simões; Siu Li, Máximo; Hernandes, Antônio Carlos
Fonte: Dyes and Pigments. Unidade: IFSC
Assuntos: NANOTECNOLOGIA, FILMES FINOS, POLÍMEROS (MATERIAIS), PIGMENTOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDI, Maria Inês Basso et al. Colored films produced by electron beam deposition from nanometric Ti'O IND. 2' and 'Al IND. 2''O IND. 3' pigment powders obtained by modified polymeric precursor method. Dyes and Pigments, v. 75, n. 3, p. 693-700, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2006.07.022. Acesso em: 25 jul. 2024.
APA
Bernardi, M. I. B., De Vicente, F. S., Siu Li, M., & Hernandes, A. C. (2007). Colored films produced by electron beam deposition from nanometric Ti'O IND. 2' and 'Al IND. 2''O IND. 3' pigment powders obtained by modified polymeric precursor method. Dyes and Pigments, 75( 3), 693-700. doi:10.1016/j.dyepig.2006.07.022
NLM
Bernardi MIB, De Vicente FS, Siu Li M, Hernandes AC. Colored films produced by electron beam deposition from nanometric Ti'O IND. 2' and 'Al IND. 2''O IND. 3' pigment powders obtained by modified polymeric precursor method [Internet]. Dyes and Pigments. 2007 ; 75( 3): 693-700.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2006.07.022
Vancouver
Bernardi MIB, De Vicente FS, Siu Li M, Hernandes AC. Colored films produced by electron beam deposition from nanometric Ti'O IND. 2' and 'Al IND. 2''O IND. 3' pigment powders obtained by modified polymeric precursor method [Internet]. Dyes and Pigments. 2007 ; 75( 3): 693-700.[citado 2024 jul. 25 ] Available from: https://doi.org/10.1016/j.dyepig.2006.07.022

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