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  • Source: Magnetic Resonance in Chemistry. Unidade: IQ

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, ÁCIDOS CARBOXÍLICOS

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      DOMINGUES, Nelson Luís de Campos et al. Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some alpha-arylthio and alpha-arylsulfonyl substituted N-methoxy-N-methyl propionamides. Magnetic Resonance in Chemistry, v. 45, n. 1, p. 87-89, 2007Tradução . . Acesso em: 23 ago. 2024.
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      Domingues, N. L. de C., Mondino, M. G., Reis, A. K. C. A., Rittner, R., Lima, F. da S., & Olivato, P. R. (2007). Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some alpha-arylthio and alpha-arylsulfonyl substituted N-methoxy-N-methyl propionamides. Magnetic Resonance in Chemistry, 45( 1), 87-89.
    • NLM

      Domingues NL de C, Mondino MG, Reis AKCA, Rittner R, Lima F da S, Olivato PR. Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some alpha-arylthio and alpha-arylsulfonyl substituted N-methoxy-N-methyl propionamides. Magnetic Resonance in Chemistry. 2007 ; 45( 1): 87-89.[citado 2024 ago. 23 ]
    • Vancouver

      Domingues NL de C, Mondino MG, Reis AKCA, Rittner R, Lima F da S, Olivato PR. Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some alpha-arylthio and alpha-arylsulfonyl substituted N-methoxy-N-methyl propionamides. Magnetic Resonance in Chemistry. 2007 ; 45( 1): 87-89.[citado 2024 ago. 23 ]
  • Source: Luminescence. Unidade: IQ

    Subjects: SOLUÇÕES AQUOSAS, OXIGÊNIO, OXIDAÇÃO

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      BASTOS, Erick Leite et al. Studies on PVP hydrogel-supported luminol chemiluminescence: 1. Kinetic and mechanistic aspects using multivariate factorial analysis. Luminescence, v. 22, n. 2, p. 113-125, 2007Tradução . . Disponível em: https://doi.org/10.1002/bio.934. Acesso em: 23 ago. 2024.
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      Bastos, E. L., Ciscato, L. F. M. L., Bartoloni, F. H., Catalani, L. H., & Baader, W. J. (2007). Studies on PVP hydrogel-supported luminol chemiluminescence: 1. Kinetic and mechanistic aspects using multivariate factorial analysis. Luminescence, 22( 2), 113-125. doi:10.1002/bio.934
    • NLM

      Bastos EL, Ciscato LFML, Bartoloni FH, Catalani LH, Baader WJ. Studies on PVP hydrogel-supported luminol chemiluminescence: 1. Kinetic and mechanistic aspects using multivariate factorial analysis [Internet]. Luminescence. 2007 ; 22( 2): 113-125.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/bio.934
    • Vancouver

      Bastos EL, Ciscato LFML, Bartoloni FH, Catalani LH, Baader WJ. Studies on PVP hydrogel-supported luminol chemiluminescence: 1. Kinetic and mechanistic aspects using multivariate factorial analysis [Internet]. Luminescence. 2007 ; 22( 2): 113-125.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/bio.934
  • Source: Luminescence. Unidade: IQ

    Subjects: ANÁLISE EM FLUXO CONTÍNUO, OXIDAÇÃO, VITAMINA E (ANÁLOGOS E DERIVADOS)

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      BASTOS, Erick Leite et al. Studies on PVP hydrogel-supported luminol chemiluminescence: 2. Luminometer calibration and potential analytical applications. Luminescence, v. 22, n. 2, p. 126-133, 2007Tradução . . Disponível em: https://doi.org/10.1002/bio.935. Acesso em: 23 ago. 2024.
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      Bastos, E. L., Ciscato, L. F. M. L., Bartoloni, F. H., Catalani, L. H., Romoff, P., & Baader, W. J. (2007). Studies on PVP hydrogel-supported luminol chemiluminescence: 2. Luminometer calibration and potential analytical applications. Luminescence, 22( 2), 126-133. doi:10.1002/bio.935
    • NLM

      Bastos EL, Ciscato LFML, Bartoloni FH, Catalani LH, Romoff P, Baader WJ. Studies on PVP hydrogel-supported luminol chemiluminescence: 2. Luminometer calibration and potential analytical applications [Internet]. Luminescence. 2007 ; 22( 2): 126-133.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/bio.935
    • Vancouver

      Bastos EL, Ciscato LFML, Bartoloni FH, Catalani LH, Romoff P, Baader WJ. Studies on PVP hydrogel-supported luminol chemiluminescence: 2. Luminometer calibration and potential analytical applications [Internet]. Luminescence. 2007 ; 22( 2): 126-133.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/bio.935
  • Source: Journal of Peptide Science. Unidade: IQ

    Subjects: PEPTÍDEOS (SÍNTESE), BIOQUÍMICA

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      PROTI, Patrícia Barrientos e REMUZGO, César e MIRANDA, Maria Terêsa Machini de. Comparison of procedures for directly obtaining protected peptide acids from peptide-resins. Journal of Peptide Science, v. 13, n. 6, p. 386-392, 2007Tradução . . Disponível em: https://doi.org/10.1002/psc.856. Acesso em: 23 ago. 2024.
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      Proti, P. B., Remuzgo, C., & Miranda, M. T. M. de. (2007). Comparison of procedures for directly obtaining protected peptide acids from peptide-resins. Journal of Peptide Science, 13( 6), 386-392. doi:10.1002/psc.856
    • NLM

      Proti PB, Remuzgo C, Miranda MTM de. Comparison of procedures for directly obtaining protected peptide acids from peptide-resins [Internet]. Journal of Peptide Science. 2007 ; 13( 6): 386-392.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/psc.856
    • Vancouver

      Proti PB, Remuzgo C, Miranda MTM de. Comparison of procedures for directly obtaining protected peptide acids from peptide-resins [Internet]. Journal of Peptide Science. 2007 ; 13( 6): 386-392.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/psc.856
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: SOLUBILIDADE, FÍSICO-QUÍMICA

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      PALATINUS, Joseph A. et al. An improved characteristic molecular volume parameter for linear solvation energy relationships of acyclic alkanes. Journal of Physical Organic Chemistry, v. 19, n. 11, p. 725-730, 2006Tradução . . Disponível em: https://doi.org/10.1002/poc.1065. Acesso em: 23 ago. 2024.
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      Palatinus, J. A., Caroll, F. A., Argenton, A. B., & Quina, F. H. (2006). An improved characteristic molecular volume parameter for linear solvation energy relationships of acyclic alkanes. Journal of Physical Organic Chemistry, 19( 11), 725-730. doi:10.1002/poc.1065
    • NLM

      Palatinus JA, Caroll FA, Argenton AB, Quina FH. An improved characteristic molecular volume parameter for linear solvation energy relationships of acyclic alkanes [Internet]. Journal of Physical Organic Chemistry. 2006 ; 19( 11): 725-730.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.1065
    • Vancouver

      Palatinus JA, Caroll FA, Argenton AB, Quina FH. An improved characteristic molecular volume parameter for linear solvation energy relationships of acyclic alkanes [Internet]. Journal of Physical Organic Chemistry. 2006 ; 19( 11): 725-730.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.1065
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: SOLVENTE, HIDRÓLISE

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      EL SEOUD, Omar A e SIVIERO, Fábio. Kinetics of the pH-independent hydrolyses of 4-nitrophenyl chloroformate and 4-nitrophenyl heptafluorobutyrate in water-acetonitrile mixtures: consequences of solvent composition and ester hydrophobicity. Journal of Physical Organic Chemistry, v. 19, n. 11, p. 793-802, 2006Tradução . . Disponível em: https://doi.org/10.1002/poc.1081. Acesso em: 23 ago. 2024.
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      El Seoud, O. A., & Siviero, F. (2006). Kinetics of the pH-independent hydrolyses of 4-nitrophenyl chloroformate and 4-nitrophenyl heptafluorobutyrate in water-acetonitrile mixtures: consequences of solvent composition and ester hydrophobicity. Journal of Physical Organic Chemistry, 19( 11), 793-802. doi:10.1002/poc.1081
    • NLM

      El Seoud OA, Siviero F. Kinetics of the pH-independent hydrolyses of 4-nitrophenyl chloroformate and 4-nitrophenyl heptafluorobutyrate in water-acetonitrile mixtures: consequences of solvent composition and ester hydrophobicity [Internet]. Journal of Physical Organic Chemistry. 2006 ; 19( 11): 793-802.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.1081
    • Vancouver

      El Seoud OA, Siviero F. Kinetics of the pH-independent hydrolyses of 4-nitrophenyl chloroformate and 4-nitrophenyl heptafluorobutyrate in water-acetonitrile mixtures: consequences of solvent composition and ester hydrophobicity [Internet]. Journal of Physical Organic Chemistry. 2006 ; 19( 11): 793-802.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.1081
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      BLAGOEVA, Iva B. et al. Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis. Journal of Physical Organic Chemistry, v. 18, n. 8, p. 850-855, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.953. Acesso em: 23 ago. 2024.
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      Blagoeva, I. B., Ouarti, N., El Seoud, O. A., & Ruasse, M. -F. (2005). Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis. Journal of Physical Organic Chemistry, 18( 8), 850-855. doi:10.1002/poc.953
    • NLM

      Blagoeva IB, Ouarti N, El Seoud OA, Ruasse M-F. Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 8): 850-855.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.953
    • Vancouver

      Blagoeva IB, Ouarti N, El Seoud OA, Ruasse M-F. Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 8): 850-855.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.953
  • Source: Luminescence. Unidade: IQ

    Subjects: RUTÊNIO, NÍQUEL, REAÇÕES QUÍMICAS

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      BONIFÁCIO, Rodrigo Leandro e COICHEV, Nina. Chemiluminescent reaction of sulphite auto-oxidation in the presence of Ni(II)/tetraglycine and ruthenium(II)/bipy complexes: mechanistic considerations. Luminescence, v. 20, n. 6, p. 428-434, 2005Tradução . . Disponível em: https://doi.org/10.1002/bio.868. Acesso em: 23 ago. 2024.
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      Bonifácio, R. L., & Coichev, N. (2005). Chemiluminescent reaction of sulphite auto-oxidation in the presence of Ni(II)/tetraglycine and ruthenium(II)/bipy complexes: mechanistic considerations. Luminescence, 20( 6), 428-434. doi:10.1002/bio.868
    • NLM

      Bonifácio RL, Coichev N. Chemiluminescent reaction of sulphite auto-oxidation in the presence of Ni(II)/tetraglycine and ruthenium(II)/bipy complexes: mechanistic considerations [Internet]. Luminescence. 2005 ; 20( 6): 428-434.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/bio.868
    • Vancouver

      Bonifácio RL, Coichev N. Chemiluminescent reaction of sulphite auto-oxidation in the presence of Ni(II)/tetraglycine and ruthenium(II)/bipy complexes: mechanistic considerations [Internet]. Luminescence. 2005 ; 20( 6): 428-434.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/bio.868
  • Source: Physica Status Solidi A - Applied Research. Unidades: FFCLRP, IQ

    Subjects: SEMICONDUTORES, TRANSISTORES

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      MERUVIA, Michelle Sostag et al. Magnetoresistive hybrid transistor in vertical architecture. Physica Status Solidi A - Applied Research, v. 202, n. 14, p. R158-R160, 2005Tradução . . Disponível em: https://doi.org/10.1002/pssa.200521270. Acesso em: 23 ago. 2024.
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      Meruvia, M. S., Benvenho, A. R. V., Hümmelgen, I. A., Gómez, J. A., Graeff, C. F. de O., Li, R. W. C., et al. (2005). Magnetoresistive hybrid transistor in vertical architecture. Physica Status Solidi A - Applied Research, 202( 14), R158-R160. doi:10.1002/pssa.200521270
    • NLM

      Meruvia MS, Benvenho ARV, Hümmelgen IA, Gómez JA, Graeff CF de O, Li RWC, Aguiar LHJ de M da C, Gruber J. Magnetoresistive hybrid transistor in vertical architecture [Internet]. Physica Status Solidi A - Applied Research. 2005 ; 202( 14): R158-R160.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/pssa.200521270
    • Vancouver

      Meruvia MS, Benvenho ARV, Hümmelgen IA, Gómez JA, Graeff CF de O, Li RWC, Aguiar LHJ de M da C, Gruber J. Magnetoresistive hybrid transistor in vertical architecture [Internet]. Physica Status Solidi A - Applied Research. 2005 ; 202( 14): R158-R160.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/pssa.200521270
  • Source: Journal of Peptide Science. Unidade: IQ

    Subjects: PEPTÍDEOS, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      VALENTE, Ana Paula et al. Study of the effect of the peptide loading and solvent system in SPPS by HRMAS-NMR. Journal of Peptide Science, v. 11, n. 9, p. 556-563, 2005Tradução . . Disponível em: https://doi.org/10.1002/psc.659. Acesso em: 23 ago. 2024.
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      Valente, A. P., Almeida, F. C. L. de, Nakaie, C. R., Schreier, S., Crusca Junior, E., & Cilli, E. M. (2005). Study of the effect of the peptide loading and solvent system in SPPS by HRMAS-NMR. Journal of Peptide Science, 11( 9), 556-563. doi:10.1002/psc.659
    • NLM

      Valente AP, Almeida FCL de, Nakaie CR, Schreier S, Crusca Junior E, Cilli EM. Study of the effect of the peptide loading and solvent system in SPPS by HRMAS-NMR [Internet]. Journal of Peptide Science. 2005 ; 11( 9): 556-563.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/psc.659
    • Vancouver

      Valente AP, Almeida FCL de, Nakaie CR, Schreier S, Crusca Junior E, Cilli EM. Study of the effect of the peptide loading and solvent system in SPPS by HRMAS-NMR [Internet]. Journal of Peptide Science. 2005 ; 11( 9): 556-563.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/psc.659
  • Source: Magnetic Resonance in Chemistry. Unidade: IQ

    Subjects: ESPECTROSCOPIA DE RESSONÂNCIA MAGNÉTICA NUCLEAR, SÍNTESE ORGÂNICA

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      REIS, Adriana Karla Cardoso Amorim e OLIVATO, Paulo Roberto e RITTNER, Roberto. Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some 4 '-substituted diethyl 1-methylthio- and diethyl 1-methylsulfonyl-2-oxo-2-phenylethylphosphonates. Magnetic Resonance in Chemistry, v. 43, n. 1, p. 85-88, 2005Tradução . . Acesso em: 23 ago. 2024.
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      Reis, A. K. C. A., Olivato, P. R., & Rittner, R. (2005). Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some 4 '-substituted diethyl 1-methylthio- and diethyl 1-methylsulfonyl-2-oxo-2-phenylethylphosphonates. Magnetic Resonance in Chemistry, 43( 1), 85-88.
    • NLM

      Reis AKCA, Olivato PR, Rittner R. Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some 4 '-substituted diethyl 1-methylthio- and diethyl 1-methylsulfonyl-2-oxo-2-phenylethylphosphonates. Magnetic Resonance in Chemistry. 2005 ; 43( 1): 85-88.[citado 2024 ago. 23 ]
    • Vancouver

      Reis AKCA, Olivato PR, Rittner R. Complete assignment of 'ANTPOT. 1 H' and 'ANTPOT. 13 C' NMR spectra of some 4 '-substituted diethyl 1-methylthio- and diethyl 1-methylsulfonyl-2-oxo-2-phenylethylphosphonates. Magnetic Resonance in Chemistry. 2005 ; 43( 1): 85-88.[citado 2024 ago. 23 ]
  • Source: Journal of Polymer Science. Part A: Polymer Chemistry. Unidade: IQ

    Subjects: NANOCOMPOSITOS, ESPECTROSCOPIA RAMAN

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      DO NASCIMENTO, G. M. et al. Synthesis and characterization of single-wall-carbon-nanotube-doped emeraldine salt and base polyaniline nanocomposites. Journal of Polymer Science. Part A: Polymer Chemistry, v. 43, n. 4, p. 815-822, 2005Tradução . . Disponível em: https://doi.org/10.1002/pola.20551. Acesso em: 23 ago. 2024.
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      Do Nascimento, G. M., Corio, P., Novickis, R. W., Temperini, M. L. A., & Dresselhaus, M. S. (2005). Synthesis and characterization of single-wall-carbon-nanotube-doped emeraldine salt and base polyaniline nanocomposites. Journal of Polymer Science. Part A: Polymer Chemistry, 43( 4), 815-822. doi:10.1002/pola.20551
    • NLM

      Do Nascimento GM, Corio P, Novickis RW, Temperini MLA, Dresselhaus MS. Synthesis and characterization of single-wall-carbon-nanotube-doped emeraldine salt and base polyaniline nanocomposites [Internet]. Journal of Polymer Science. Part A: Polymer Chemistry. 2005 ; 43( 4): 815-822.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/pola.20551
    • Vancouver

      Do Nascimento GM, Corio P, Novickis RW, Temperini MLA, Dresselhaus MS. Synthesis and characterization of single-wall-carbon-nanotube-doped emeraldine salt and base polyaniline nanocomposites [Internet]. Journal of Polymer Science. Part A: Polymer Chemistry. 2005 ; 43( 4): 815-822.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/pola.20551
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: ÁLCOOL, QUÍMICA ORGÂNICA

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      TADA, Erika Batista e SILVA, Priscilla Leandro e EL SEOUD, Omar A. Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions. Journal of Physical Organic Chemistry, v. 18, n. 5, p. 398-407, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.887. Acesso em: 23 ago. 2024.
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      Tada, E. B., Silva, P. L., & El Seoud, O. A. (2005). Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions. Journal of Physical Organic Chemistry, 18( 5), 398-407. doi:10.1002/poc.887
    • NLM

      Tada EB, Silva PL, El Seoud OA. Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 5): 398-407.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.887
    • Vancouver

      Tada EB, Silva PL, El Seoud OA. Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 5): 398-407.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.887
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: HIDRÓLISE, QUÍMICA ORGÂNICA

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      EL SEOUD, Omar A et al. Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group. Journal of Physical Organic Chemistry, v. 18, n. 2, p. 173-182, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.864. Acesso em: 23 ago. 2024.
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      El Seoud, O. A., Ferreira, M., Rodrigues, W. A., & Ruasse, M. -F. (2005). Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group. Journal of Physical Organic Chemistry, 18( 2), 173-182. doi:10.1002/poc.864
    • NLM

      El Seoud OA, Ferreira M, Rodrigues WA, Ruasse M-F. Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 2): 173-182.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.864
    • Vancouver

      El Seoud OA, Ferreira M, Rodrigues WA, Ruasse M-F. Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 2): 173-182.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.864
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SOLVENTE, FÍSICO-QUÍMICA

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      MARTINS, Clarissa T. e LIMA, Michelle de Souza e EL SEOUD, Omar A. A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle. Journal of Physical Organic Chemistry, v. 18, n. 11, p. 1072-1085, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.975. Acesso em: 23 ago. 2024.
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      Martins, C. T., Lima, M. de S., & El Seoud, O. A. (2005). A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle. Journal of Physical Organic Chemistry, 18( 11), 1072-1085. doi:10.1002/poc.975
    • NLM

      Martins CT, Lima M de S, El Seoud OA. A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 11): 1072-1085.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.975
    • Vancouver

      Martins CT, Lima M de S, El Seoud OA. A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 11): 1072-1085.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/poc.975

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