Filtros : "Dyes and Pigments" Removidos: "Brasil" "Oliveira, Hueder P. M." Limpar

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  • Fonte: Dyes and Pigments. Unidade: IQ

    Assuntos: MATERIAIS NANOESTRUTURADOS, FLUORESCÊNCIA

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://dx.doi.org/10.1016/j.dyepig.2023.111754
  • 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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109972
  • 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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2021.109820
  • 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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2020.109131
  • Fonte: Dyes and Pigments. Unidade: IQ

    Assuntos: HIDRÓLISE, FLUORESCÊNCIA, PRODUTOS NATURAIS

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108609
  • Fonte: Dyes and Pigments. Unidade: FFCLRP

    Assuntos: FITOTERAPIA, NANOTECNOLOGIA, NEOPLASIAS

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107940
  • Fonte: Dyes and Pigments. Unidade: IQ

    Assuntos: OXIDAÇÃO, TELÚRIO, MERCÚRIO (ELEMENTO QUÍMICO)

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2018.07.055
  • Fonte: Dyes and Pigments. Unidade: IQ

    Assuntos: TELÚRIO, MERCÚRIO (ELEMENTO QUÍMICO)

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2018.06.005
  • Fonte: Dyes and Pigments. Unidade: IFSC

    Assuntos: FOTOLUMINESCÊNCIA, VIDROS METÁLICOS

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2018.07.020
  • Fonte: Dyes and Pigments. Unidade: IQ

    Assunto: FLUORESCÊNCIA

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2016.02.032
  • Fonte: Dyes and Pigments. Unidade: IQ

    Assuntos: FLUORESCÊNCIA, SOLVENTE

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2015.03.004
  • Fonte: Dyes and Pigments. Unidade: FFCLRP

    Assuntos: LIPOSSOMOS, MELANOMA, TERAPIA FOTODINÂMICA, ENGENHARIA TECIDUAL

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.08.018
  • Fonte: Dyes and Pigments. Unidade: IQ

    Assuntos: FLUORESCÊNCIA, MERCÚRIO (ELEMENTO QUÍMICO)

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.09.019
  • Fonte: Dyes and Pigments. Unidade: IFSC

    Assuntos: FLUORESCÊNCIA, ABSORÇÃO DA LUZ, FOTÔNICA

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.10.026
  • Fonte: Dyes and Pigments. Unidades: IQ, FFCLRP

    Assunto: FOTOQUÍMICA

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
  • Fonte: Dyes and Pigments. Unidade: FFCLRP

    Assuntos: CÉRIO, NANOPARTÍCULAS, TERRAS RARAS

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    • 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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2012.12.020
  • Fonte: Dyes and Pigments. Unidade: IQ

    Assuntos: LÍQUIDOS IÔNICOS, SOLVENTE

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    • ABNT

      LOFFREDO, Carina et al. β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability. Dyes and Pigments, v. 96, n. 1, p. 16-24, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2012.07.017. Acesso em: 07 nov. 2024.
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      Loffredo, C., Pires, P. A. R., Imran, M., & El Seoud, O. A. (2013). β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability. Dyes and Pigments, 96( 1), 16-24. doi:10.1016/j.dyepig.2012.07.017
    • NLM

      Loffredo C, Pires PAR, Imran M, El Seoud OA. β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability [Internet]. Dyes and Pigments. 2013 ; 96( 1): 16-24.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2012.07.017
    • Vancouver

      Loffredo C, Pires PAR, Imran M, El Seoud OA. β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability [Internet]. Dyes and Pigments. 2013 ; 96( 1): 16-24.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2012.07.017
  • Fonte: Dyes and Pigments. Unidades: IQ, FFCLRP

    Assuntos: QUÍMICA INORGÂNICA, SÍNTESE INORGÂNICA

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      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: 07 nov. 2024.
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      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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2013.05.024
  • Fonte: Dyes and Pigments. Unidade: FFCLRP

    Assuntos: BIODIESEL, FLUORESCÊNCIA, ESPECTROSCOPIA

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    • 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: 07 nov. 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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2011.05.020
  • Fonte: Dyes and Pigments. Unidade: IFSC

    Assuntos: NANOTECNOLOGIA, FILMES FINOS, POLÍMEROS (MATERIAIS), PIGMENTOS

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      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: 07 nov. 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 nov. 07 ] 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 nov. 07 ] Available from: https://doi.org/10.1016/j.dyepig.2006.07.022

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