The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions

Sodium nitroprusside (SNP, Na 2 [Fe(CN) 5 (NO)] •2H 2 O) is a widely used NO-donor hypotensive agent, containing the formally described nitrosonium (NO + ) ligand, which may be redox-interconverted to the corresponding one-electron (NO) and two-electron (NO - /HNO) reduced bound species. Thus, the c...

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Publicado: 2008
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14779226_v_n28_p3633_Olabe
http://hdl.handle.net/20.500.12110/paper_14779226_v_n28_p3633_Olabe
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spelling paper:paper_14779226_v_n28_p3633_Olabe2023-06-08T16:18:19Z The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions Sodium Coordination chemistry Cyanoferrates Relevant reactions Sodium nitroprusside (SNP) Coordination reactions antihypertensive agent ligand nitrogen oxide nitroprusside sodium animal article chemistry inorganic chemistry oxidation reduction reaction Animals Antihypertensive Agents Chemistry, Bioinorganic Ligands Nitrogen Oxides Nitroprusside Oxidation-Reduction Sodium nitroprusside (SNP, Na 2 [Fe(CN) 5 (NO)] •2H 2 O) is a widely used NO-donor hypotensive agent, containing the formally described nitrosonium (NO + ) ligand, which may be redox-interconverted to the corresponding one-electron (NO) and two-electron (NO - /HNO) reduced bound species. Thus, the chemistry of the three nitrosyl ligands may be explored with adequate, biologically relevant substrates. The nitrosonium complex, [Fe(CN) 5 (NO)] 2- , is formed through a reductive nitrosylation reaction of [Fe III (CN) 5 (H 2 O)] 2- with NO, or, alternatively, through the coordination of NO 2 - to [Fe II (CN) 5 (H 2 O)] 3- and further proton-assisted dehydration. It is extremely inert toward NO + -dissociation, and behaves as an electrophile toward different bases: OH - , amines, thiolates, etc. Also, SNP releases NO upon UV-vis photo-activation, with formation of [Fe III (CN) 5 (H 2 O)] 2- . The more electron rich [Fe(CN) 5 (NO)] 3- may be prepared from [Fe II (CN) 5 (H 2 O)] 3- and NO, and is also highly inert toward the dissociation of NO (k = 1.6 × 10 -5 s -1 , 25.0 °C, pH 10.2). It reacts with O 2 leading to SNP, with the intermediacy of a peroxynitrite adduct. The [Fe(CN) 5 (NO)] 3- ion is labile toward the release of trans-cyanide, forming the [Fe(CN) 4 (NO)] 2- ion. Both complexes exist in a pH-dependent equilibrium, and decompose thermally in the hours time scale, releasing cyanides and NO. The latter may further bind to [Fe(CN) 4 (NO)] 2- with formation of a singlet dinitrosyl species, [Fe(CN) 4 (NO) 2 ] 2- , which in turn is unstable toward disproportionation into SNP and N 2 O, and toward the parallel formation of a tetrahedral paramagnetic dinitrosyl compound, [Fe(CN) 2 (NO) 2 ]. Emerging studies with the putative nitroxyl complex, [Fe(CN) 5 (HNO)] 3- , should allow for a complete picture of the three nitrosyl ligands in the same pentacyano fragment. The present Perspective, based on an adequate characterization of structural and spectroscopic properties, will focus on the kinetic and mechanistic description of the above mentioned reactions, which display a versatile scenario, fundamentally related to the biologically relevant processes associated with NO reactivity. © 2008 The Royal Society of Chemistry. 2008 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14779226_v_n28_p3633_Olabe http://hdl.handle.net/20.500.12110/paper_14779226_v_n28_p3633_Olabe
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Sodium
Coordination chemistry
Cyanoferrates
Relevant reactions
Sodium nitroprusside (SNP)
Coordination reactions
antihypertensive agent
ligand
nitrogen oxide
nitroprusside sodium
animal
article
chemistry
inorganic chemistry
oxidation reduction reaction
Animals
Antihypertensive Agents
Chemistry, Bioinorganic
Ligands
Nitrogen Oxides
Nitroprusside
Oxidation-Reduction
spellingShingle Sodium
Coordination chemistry
Cyanoferrates
Relevant reactions
Sodium nitroprusside (SNP)
Coordination reactions
antihypertensive agent
ligand
nitrogen oxide
nitroprusside sodium
animal
article
chemistry
inorganic chemistry
oxidation reduction reaction
Animals
Antihypertensive Agents
Chemistry, Bioinorganic
Ligands
Nitrogen Oxides
Nitroprusside
Oxidation-Reduction
The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions
topic_facet Sodium
Coordination chemistry
Cyanoferrates
Relevant reactions
Sodium nitroprusside (SNP)
Coordination reactions
antihypertensive agent
ligand
nitrogen oxide
nitroprusside sodium
animal
article
chemistry
inorganic chemistry
oxidation reduction reaction
Animals
Antihypertensive Agents
Chemistry, Bioinorganic
Ligands
Nitrogen Oxides
Nitroprusside
Oxidation-Reduction
description Sodium nitroprusside (SNP, Na 2 [Fe(CN) 5 (NO)] •2H 2 O) is a widely used NO-donor hypotensive agent, containing the formally described nitrosonium (NO + ) ligand, which may be redox-interconverted to the corresponding one-electron (NO) and two-electron (NO - /HNO) reduced bound species. Thus, the chemistry of the three nitrosyl ligands may be explored with adequate, biologically relevant substrates. The nitrosonium complex, [Fe(CN) 5 (NO)] 2- , is formed through a reductive nitrosylation reaction of [Fe III (CN) 5 (H 2 O)] 2- with NO, or, alternatively, through the coordination of NO 2 - to [Fe II (CN) 5 (H 2 O)] 3- and further proton-assisted dehydration. It is extremely inert toward NO + -dissociation, and behaves as an electrophile toward different bases: OH - , amines, thiolates, etc. Also, SNP releases NO upon UV-vis photo-activation, with formation of [Fe III (CN) 5 (H 2 O)] 2- . The more electron rich [Fe(CN) 5 (NO)] 3- may be prepared from [Fe II (CN) 5 (H 2 O)] 3- and NO, and is also highly inert toward the dissociation of NO (k = 1.6 × 10 -5 s -1 , 25.0 °C, pH 10.2). It reacts with O 2 leading to SNP, with the intermediacy of a peroxynitrite adduct. The [Fe(CN) 5 (NO)] 3- ion is labile toward the release of trans-cyanide, forming the [Fe(CN) 4 (NO)] 2- ion. Both complexes exist in a pH-dependent equilibrium, and decompose thermally in the hours time scale, releasing cyanides and NO. The latter may further bind to [Fe(CN) 4 (NO)] 2- with formation of a singlet dinitrosyl species, [Fe(CN) 4 (NO) 2 ] 2- , which in turn is unstable toward disproportionation into SNP and N 2 O, and toward the parallel formation of a tetrahedral paramagnetic dinitrosyl compound, [Fe(CN) 2 (NO) 2 ]. Emerging studies with the putative nitroxyl complex, [Fe(CN) 5 (HNO)] 3- , should allow for a complete picture of the three nitrosyl ligands in the same pentacyano fragment. The present Perspective, based on an adequate characterization of structural and spectroscopic properties, will focus on the kinetic and mechanistic description of the above mentioned reactions, which display a versatile scenario, fundamentally related to the biologically relevant processes associated with NO reactivity. © 2008 The Royal Society of Chemistry.
title The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions
title_short The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions
title_full The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions
title_fullStr The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions
title_full_unstemmed The coordination chemistry of nitrosyl in cyanoferrates. An exhibit of bioinorganic relevant reactions
title_sort coordination chemistry of nitrosyl in cyanoferrates. an exhibit of bioinorganic relevant reactions
publishDate 2008
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14779226_v_n28_p3633_Olabe
http://hdl.handle.net/20.500.12110/paper_14779226_v_n28_p3633_Olabe
_version_ 1768545112429690880