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Artigo de periodico
Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis (2005)
Blagoeva, Iva B.; Ouarti, Nadia; El Seoud, Omar A ; Ruasse, Marie-Françoise
Source: Journal of Physical Organic Chemistry. Unidade: IQ
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 01 maio 2024.
APA
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 maio 01 ] 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 maio 01 ] Available from: https://doi.org/10.1002/poc.953
Artigo de periodico
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 (2005)
El Seoud, Omar A ; Ferreira, Mônica; Rodrigues, Wagner Aparecido; Ruasse, Marie-Françoise
Source: Journal of Physical Organic Chemistry. Unidade: IQ
Subjects: HIDRÓLISE, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 01 maio 2024.
APA
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 maio 01 ] 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 maio 01 ] Available from: https://doi.org/10.1002/poc.864
Artigo de periodico
Nucleophilic reactivity of the CTACI-Micelle-bound fluoride ion: the influence of water concentration and ionic strength at the micellar interface (2003)
Tada, Erika Batista; Ouarti, Nadia; Silva, Priscilla Leandro; Blagoeva, Iva B.; El Seoud, Omar A ; Ruasse, Marie-Françoise
Source: Langmuir. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SURFACTANTES, CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TADA, Erika Batista et al. Nucleophilic reactivity of the CTACI-Micelle-bound fluoride ion: the influence of water concentration and ionic strength at the micellar interface. Langmuir, v. 19, n. 26, p. 10666-10672, 2003Tradução . . Acesso em: 01 maio 2024.
APA
Tada, E. B., Ouarti, N., Silva, P. L., Blagoeva, I. B., El Seoud, O. A., & Ruasse, M. -F. (2003). Nucleophilic reactivity of the CTACI-Micelle-bound fluoride ion: the influence of water concentration and ionic strength at the micellar interface. Langmuir, 19( 26), 10666-10672.
NLM
Tada EB, Ouarti N, Silva PL, Blagoeva IB, El Seoud OA, Ruasse M-F. Nucleophilic reactivity of the CTACI-Micelle-bound fluoride ion: the influence of water concentration and ionic strength at the micellar interface. Langmuir. 2003 ; 19( 26): 10666-10672.[citado 2024 maio 01 ]
Vancouver
Tada EB, Ouarti N, Silva PL, Blagoeva IB, El Seoud OA, Ruasse M-F. Nucleophilic reactivity of the CTACI-Micelle-bound fluoride ion: the influence of water concentration and ionic strength at the micellar interface. Langmuir. 2003 ; 19( 26): 10666-10672.[citado 2024 maio 01 ]
Artigo de periodico
Kinetics and mechanism of phosphate-catalyzed hydrolysis of benzoate esters: comparison with nucleophilic catalysis by imidazole and o-iodosobenzoate (2002)
El Seoud, Omar A ; Ruasse, Marie-Françoise; Rodrigues, W. A.
Source: Journal of the Chemical Society - Perkin Transactions 2. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, ESPECTROFOTOMETRIA, FÍSICO-QUÍMICA, CATÁLISE, HIDRÓLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EL SEOUD, Omar A e RUASSE, Marie-Françoise e RODRIGUES, W. A. Kinetics and mechanism of phosphate-catalyzed hydrolysis of benzoate esters: comparison with nucleophilic catalysis by imidazole and o-iodosobenzoate. Journal of the Chemical Society - Perkin Transactions 2, n. 6, p. 1053-1058, 2002Tradução . . Disponível em: https://doi.org/10.1039/b202728n. Acesso em: 01 maio 2024.
APA
El Seoud, O. A., Ruasse, M. -F., & Rodrigues, W. A. (2002). Kinetics and mechanism of phosphate-catalyzed hydrolysis of benzoate esters: comparison with nucleophilic catalysis by imidazole and o-iodosobenzoate. Journal of the Chemical Society - Perkin Transactions 2, ( 6), 1053-1058. doi:10.1039/b202728n
NLM
El Seoud OA, Ruasse M-F, Rodrigues WA. Kinetics and mechanism of phosphate-catalyzed hydrolysis of benzoate esters: comparison with nucleophilic catalysis by imidazole and o-iodosobenzoate [Internet]. Journal of the Chemical Society - Perkin Transactions 2. 2002 ;( 6): 1053-1058.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/b202728n
Vancouver
El Seoud OA, Ruasse M-F, Rodrigues WA. Kinetics and mechanism of phosphate-catalyzed hydrolysis of benzoate esters: comparison with nucleophilic catalysis by imidazole and o-iodosobenzoate [Internet]. Journal of the Chemical Society - Perkin Transactions 2. 2002 ;( 6): 1053-1058.[citado 2024 maio 01 ] Available from: https://doi.org/10.1039/b202728n
Artigo de periodico
pH-independent hydrolysis of 4-nitrophenyl 2,2-dichloropropinate in aqueous micellar solutions: realtive contributions of hydrophobic and electrostatic interactions (2001)
El Seoud, Omar A ; Ruasse, Marie-Françoise; Possidonio, Shirley
Source: Journal of Physical Organic Chemistry. Unidade: IQ
Subjects: SURFACTANTES, HIDRÓLISE, CINÉTICA, FÍSICO-QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EL SEOUD, Omar A e RUASSE, Marie-Françoise e POSSIDONIO, Shirley. pH-independent hydrolysis of 4-nitrophenyl 2,2-dichloropropinate in aqueous micellar solutions: realtive contributions of hydrophobic and electrostatic interactions. Journal of Physical Organic Chemistry, v. 14, n. 8, p. 526-532, 2001Tradução . . Disponível em: https://doi.org/10.1002/poc.384. Acesso em: 01 maio 2024.
APA
El Seoud, O. A., Ruasse, M. -F., & Possidonio, S. (2001). pH-independent hydrolysis of 4-nitrophenyl 2,2-dichloropropinate in aqueous micellar solutions: realtive contributions of hydrophobic and electrostatic interactions. Journal of Physical Organic Chemistry, 14( 8), 526-532. doi:10.1002/poc.384
NLM
El Seoud OA, Ruasse M-F, Possidonio S. pH-independent hydrolysis of 4-nitrophenyl 2,2-dichloropropinate in aqueous micellar solutions: realtive contributions of hydrophobic and electrostatic interactions [Internet]. Journal of Physical Organic Chemistry. 2001 ; 14( 8): 526-532.[citado 2024 maio 01 ] Available from: https://doi.org/10.1002/poc.384
Vancouver
El Seoud OA, Ruasse M-F, Possidonio S. pH-independent hydrolysis of 4-nitrophenyl 2,2-dichloropropinate in aqueous micellar solutions: realtive contributions of hydrophobic and electrostatic interactions [Internet]. Journal of Physical Organic Chemistry. 2001 ; 14( 8): 526-532.[citado 2024 maio 01 ] Available from: https://doi.org/10.1002/poc.384
Artigo de periodico
Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8 (2001)
Ouarti, Nadia; Blagoeva, Iva B.; El Seoud, Omar A ; Ruasse, Marie-Françoise
Source: Journal of Physical Organic Chemistry. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, SOLUÇÕES AQUOSAS, SURFACTANTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OUARTI, Nadia et al. Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8. Journal of Physical Organic Chemistry, v. 14, n. 11, p. 823-831, 2001Tradução . . Disponível em: https://doi.org/10.1002/poc.441.abs. Acesso em: 01 maio 2024.
APA
Ouarti, N., Blagoeva, I. B., El Seoud, O. A., & Ruasse, M. -F. (2001). Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8. Journal of Physical Organic Chemistry, 14( 11), 823-831. doi:10.1002/poc.441.abs
NLM
Ouarti N, Blagoeva IB, El Seoud OA, Ruasse M-F. Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8 [Internet]. Journal of Physical Organic Chemistry. 2001 ; 14( 11): 823-831.[citado 2024 maio 01 ] Available from: https://doi.org/10.1002/poc.441.abs
Vancouver
Ouarti N, Blagoeva IB, El Seoud OA, Ruasse M-F. Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8 [Internet]. Journal of Physical Organic Chemistry. 2001 ; 14( 11): 823-831.[citado 2024 maio 01 ] Available from: https://doi.org/10.1002/poc.441.abs

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