The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates
The electrophilic reactivity of the pentacyanonitrosylferrate(II) ion, [Fe(CN)5NO]2-, toward hydrazine (Hz) and substituted hydrazines (MeHz, 1, 1-Me2Hz, and 1,2-Me2Hz) has been studied by means of stoichiometric and kinetic experiments (pH 6-10). The reaction of Hz led to N2O and NH3, with similar...
| Autor principal: | |
|---|---|
| Publicado: |
2002
|
| Materias: | |
| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00027863_v124_n35_p10307_Gutierrez http://hdl.handle.net/20.500.12110/paper_00027863_v124_n35_p10307_Gutierrez |
| Aporte de: |
| id |
paper:paper_00027863_v124_n35_p10307_Gutierrez |
|---|---|
| record_format |
dspace |
| spelling |
paper:paper_00027863_v124_n35_p10307_Gutierrez2023-06-08T14:22:38Z The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates Olabe Iparraguirre, Jose Antonio Electrophilic reactivity Decomposition Derivatives Enzymes Hydrazine Rate constants Chemical reactions amine ammonium derivative ferric ion hydrazine hydrazine derivative hydroxylamine nitrate nitric oxide nitric oxide reductase nitrite nitroprusside sodium nitrous oxide pentacyanonitrosylferrate(ii) tempol unclassified drug article binding kinetics catalysis chemical binding chemical reaction chemical reaction kinetics computer prediction decomposition electric conductivity intermethod comparison isomerism methylation product recovery reaction analysis reaction optimization reduction stoichiometry theory The electrophilic reactivity of the pentacyanonitrosylferrate(II) ion, [Fe(CN)5NO]2-, toward hydrazine (Hz) and substituted hydrazines (MeHz, 1, 1-Me2Hz, and 1,2-Me2Hz) has been studied by means of stoichiometric and kinetic experiments (pH 6-10). The reaction of Hz led to N2O and NH3, with similar paths for MeHz and 1,1-Me2Hz, which form the corresponding amines. A parallel path has been found for MeHz, leading to N2O, N2, and MeOH. The reaction of 1,2-Me2Hz follows a different route, characterized by azomethane formation (MeNNMe), full reduction of nitrosyl to NH3, and intermediate detection of [Fe(CN)5NO]3-. In the above reactions, [Fe(CN)5H2O]3- was always a product, allowing the system to proceed catalytically for nitrite reduction, an issue relevant in relation to the behavior of the nitrite and nitric oxide reductase enzymes. The mechanism comprises initial reversible adduct formation through the binding of the nucleophile to the N-atom of nitrosyl. The adducts decompose through OH- attack giving the final products, without intermediate detection. Rate constants for the adduct-formation steps (k = 0.43 M-1 s-1, 25 °C for Hz) decrease with methylation by about an order of magnitude. Among the different systems studied, one-, two-, and multielectron reductions of bound NO+ are analyzed comparatively, with consideration of the role of NO, HNO (nitroxyl), and hydroxylamine as bound intermediates. A DFT study (B3LYP) of the reaction profile allows one to characterize intermediates in the potential hypersurface. These are the initial adducts, as well as their decomposition products, the η1- and η2-linkage isomers of N2O. Fil:Olabe, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2002 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00027863_v124_n35_p10307_Gutierrez http://hdl.handle.net/20.500.12110/paper_00027863_v124_n35_p10307_Gutierrez |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Electrophilic reactivity Decomposition Derivatives Enzymes Hydrazine Rate constants Chemical reactions amine ammonium derivative ferric ion hydrazine hydrazine derivative hydroxylamine nitrate nitric oxide nitric oxide reductase nitrite nitroprusside sodium nitrous oxide pentacyanonitrosylferrate(ii) tempol unclassified drug article binding kinetics catalysis chemical binding chemical reaction chemical reaction kinetics computer prediction decomposition electric conductivity intermethod comparison isomerism methylation product recovery reaction analysis reaction optimization reduction stoichiometry theory |
| spellingShingle |
Electrophilic reactivity Decomposition Derivatives Enzymes Hydrazine Rate constants Chemical reactions amine ammonium derivative ferric ion hydrazine hydrazine derivative hydroxylamine nitrate nitric oxide nitric oxide reductase nitrite nitroprusside sodium nitrous oxide pentacyanonitrosylferrate(ii) tempol unclassified drug article binding kinetics catalysis chemical binding chemical reaction chemical reaction kinetics computer prediction decomposition electric conductivity intermethod comparison isomerism methylation product recovery reaction analysis reaction optimization reduction stoichiometry theory Olabe Iparraguirre, Jose Antonio The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates |
| topic_facet |
Electrophilic reactivity Decomposition Derivatives Enzymes Hydrazine Rate constants Chemical reactions amine ammonium derivative ferric ion hydrazine hydrazine derivative hydroxylamine nitrate nitric oxide nitric oxide reductase nitrite nitroprusside sodium nitrous oxide pentacyanonitrosylferrate(ii) tempol unclassified drug article binding kinetics catalysis chemical binding chemical reaction chemical reaction kinetics computer prediction decomposition electric conductivity intermethod comparison isomerism methylation product recovery reaction analysis reaction optimization reduction stoichiometry theory |
| description |
The electrophilic reactivity of the pentacyanonitrosylferrate(II) ion, [Fe(CN)5NO]2-, toward hydrazine (Hz) and substituted hydrazines (MeHz, 1, 1-Me2Hz, and 1,2-Me2Hz) has been studied by means of stoichiometric and kinetic experiments (pH 6-10). The reaction of Hz led to N2O and NH3, with similar paths for MeHz and 1,1-Me2Hz, which form the corresponding amines. A parallel path has been found for MeHz, leading to N2O, N2, and MeOH. The reaction of 1,2-Me2Hz follows a different route, characterized by azomethane formation (MeNNMe), full reduction of nitrosyl to NH3, and intermediate detection of [Fe(CN)5NO]3-. In the above reactions, [Fe(CN)5H2O]3- was always a product, allowing the system to proceed catalytically for nitrite reduction, an issue relevant in relation to the behavior of the nitrite and nitric oxide reductase enzymes. The mechanism comprises initial reversible adduct formation through the binding of the nucleophile to the N-atom of nitrosyl. The adducts decompose through OH- attack giving the final products, without intermediate detection. Rate constants for the adduct-formation steps (k = 0.43 M-1 s-1, 25 °C for Hz) decrease with methylation by about an order of magnitude. Among the different systems studied, one-, two-, and multielectron reductions of bound NO+ are analyzed comparatively, with consideration of the role of NO, HNO (nitroxyl), and hydroxylamine as bound intermediates. A DFT study (B3LYP) of the reaction profile allows one to characterize intermediates in the potential hypersurface. These are the initial adducts, as well as their decomposition products, the η1- and η2-linkage isomers of N2O. |
| author |
Olabe Iparraguirre, Jose Antonio |
| author_facet |
Olabe Iparraguirre, Jose Antonio |
| author_sort |
Olabe Iparraguirre, Jose Antonio |
| title |
The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates |
| title_short |
The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates |
| title_full |
The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates |
| title_fullStr |
The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates |
| title_full_unstemmed |
The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of η1-, η2-N2O bound intermediates |
| title_sort |
electrophilic reactions of pentacyanonitrosylferrate(ii) with hydrazine and substituted derivatives. catalytic reduction of nitrite and theoretical prediction of η1-, η2-n2o bound intermediates |
| publishDate |
2002 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00027863_v124_n35_p10307_Gutierrez http://hdl.handle.net/20.500.12110/paper_00027863_v124_n35_p10307_Gutierrez |
| work_keys_str_mv |
AT olabeiparraguirrejoseantonio theelectrophilicreactionsofpentacyanonitrosylferrateiiwithhydrazineandsubstitutedderivativescatalyticreductionofnitriteandtheoreticalpredictionofē1ē2n2oboundintermediates AT olabeiparraguirrejoseantonio electrophilicreactionsofpentacyanonitrosylferrateiiwithhydrazineandsubstitutedderivativescatalyticreductionofnitriteandtheoreticalpredictionofē1ē2n2oboundintermediates |
| _version_ |
1768545579502141440 |