The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals

The photodetachment of NO from [MII(CN5NO]2- with M = Fe, Ru, and Os, upon laser excitation at various wavelengths (355, 420, and 480 nm) was followed by various techniques. The three complexes showed a wavelength-dependent quantum yield of NO production Φ (NO), as measured with an NO-sensitive elec...

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Autores principales: Videla, M., Braslavsky, S.E., Olabe, J.A.
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Mus
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_1474905X_v4_n1_p75_Videla
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spelling todo:paper_1474905X_v4_n1_p75_Videla2023-10-03T16:18:28Z The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals Videla, M. Braslavsky, S.E. Olabe, J.A. iron complex nitric oxide osmium derivative ruthenium complex water absorption article chemical bond complex formation controlled study electrode enthalpy fluorescence spectroscopy hydrogen bond infrared spectroscopy laser induced optoacoustic spectroscopy low temperature procedures mathematical computing measurement photochemistry photon priority journal quantum yield spectral sensitivity spectroscopy temperature dependence ultraviolet spectrophotometry Cyanides Lasers Metals, Heavy Nitric Oxide Nitroso Compounds Organometallic Compounds Photochemistry Quantum Theory Spectrum Analysis Mus The photodetachment of NO from [MII(CN5NO]2- with M = Fe, Ru, and Os, upon laser excitation at various wavelengths (355, 420, and 480 nm) was followed by various techniques. The three complexes showed a wavelength-dependent quantum yield of NO production Φ (NO), as measured with an NO-sensitive electrode, the highest values corresponding to the larger photon energies. For the same excitation wavelength the decrease of Φ (NO) at 20 °C in the order Fe > Ru ≫ Os, is explained by the increasing M-N bond strength and inertness of the heavier metals. Transient absorption data at 420 nm indicate the formation of the [MIII(CN)5H2O]2- species in less than ca. 1 μs for M = Fe and Ru. The enthalpy content of [FeIII(CN)5H2O]2- with respect to the parent [FeII(CN)5NO]2- state is (190 ± 20) kJ mol-1, as measured by laser-induced optoacoustic spectroscopy (LIOAS) upon excitation at 480 nm. The production of [FeIII(CN5H2O]2- is concomitant with an expansion of (8 ± 3) ml mol-1 consistent with an expansion of the water bound through hydrogen bonds to the CN ligands plus the difference between NO release into the bulk and water entrance into the first coordination sphere. The activated process, as indicated by the relatively strong temperature dependence of the Φ (NO) values and by the temperature dependence of the appearance of the [FeIII(CN)5H2O]2- species, as determined by LIOAS, is attributed to NO detachment in less than ca. 100 ns from the isonitrosyl (ON) ligand (MS1 state). © The Royal Society of Chemistry and Owner Societies 2005. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_1474905X_v4_n1_p75_Videla
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic iron complex
nitric oxide
osmium derivative
ruthenium complex
water
absorption
article
chemical bond
complex formation
controlled study
electrode
enthalpy
fluorescence spectroscopy
hydrogen bond
infrared spectroscopy
laser induced optoacoustic spectroscopy
low temperature procedures
mathematical computing
measurement
photochemistry
photon
priority journal
quantum yield
spectral sensitivity
spectroscopy
temperature dependence
ultraviolet spectrophotometry
Cyanides
Lasers
Metals, Heavy
Nitric Oxide
Nitroso Compounds
Organometallic Compounds
Photochemistry
Quantum Theory
Spectrum Analysis
Mus
spellingShingle iron complex
nitric oxide
osmium derivative
ruthenium complex
water
absorption
article
chemical bond
complex formation
controlled study
electrode
enthalpy
fluorescence spectroscopy
hydrogen bond
infrared spectroscopy
laser induced optoacoustic spectroscopy
low temperature procedures
mathematical computing
measurement
photochemistry
photon
priority journal
quantum yield
spectral sensitivity
spectroscopy
temperature dependence
ultraviolet spectrophotometry
Cyanides
Lasers
Metals, Heavy
Nitric Oxide
Nitroso Compounds
Organometallic Compounds
Photochemistry
Quantum Theory
Spectrum Analysis
Mus
Videla, M.
Braslavsky, S.E.
Olabe, J.A.
The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals
topic_facet iron complex
nitric oxide
osmium derivative
ruthenium complex
water
absorption
article
chemical bond
complex formation
controlled study
electrode
enthalpy
fluorescence spectroscopy
hydrogen bond
infrared spectroscopy
laser induced optoacoustic spectroscopy
low temperature procedures
mathematical computing
measurement
photochemistry
photon
priority journal
quantum yield
spectral sensitivity
spectroscopy
temperature dependence
ultraviolet spectrophotometry
Cyanides
Lasers
Metals, Heavy
Nitric Oxide
Nitroso Compounds
Organometallic Compounds
Photochemistry
Quantum Theory
Spectrum Analysis
Mus
description The photodetachment of NO from [MII(CN5NO]2- with M = Fe, Ru, and Os, upon laser excitation at various wavelengths (355, 420, and 480 nm) was followed by various techniques. The three complexes showed a wavelength-dependent quantum yield of NO production Φ (NO), as measured with an NO-sensitive electrode, the highest values corresponding to the larger photon energies. For the same excitation wavelength the decrease of Φ (NO) at 20 °C in the order Fe > Ru ≫ Os, is explained by the increasing M-N bond strength and inertness of the heavier metals. Transient absorption data at 420 nm indicate the formation of the [MIII(CN)5H2O]2- species in less than ca. 1 μs for M = Fe and Ru. The enthalpy content of [FeIII(CN)5H2O]2- with respect to the parent [FeII(CN)5NO]2- state is (190 ± 20) kJ mol-1, as measured by laser-induced optoacoustic spectroscopy (LIOAS) upon excitation at 480 nm. The production of [FeIII(CN5H2O]2- is concomitant with an expansion of (8 ± 3) ml mol-1 consistent with an expansion of the water bound through hydrogen bonds to the CN ligands plus the difference between NO release into the bulk and water entrance into the first coordination sphere. The activated process, as indicated by the relatively strong temperature dependence of the Φ (NO) values and by the temperature dependence of the appearance of the [FeIII(CN)5H2O]2- species, as determined by LIOAS, is attributed to NO detachment in less than ca. 100 ns from the isonitrosyl (ON) ligand (MS1 state). © The Royal Society of Chemistry and Owner Societies 2005.
format JOUR
author Videla, M.
Braslavsky, S.E.
Olabe, J.A.
author_facet Videla, M.
Braslavsky, S.E.
Olabe, J.A.
author_sort Videla, M.
title The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals
title_short The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals
title_full The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals
title_fullStr The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals
title_full_unstemmed The photorelease of nitrogen monoxide (NO) from pentacyanonitrosyl coordination compounds of group 8 metals
title_sort photorelease of nitrogen monoxide (no) from pentacyanonitrosyl coordination compounds of group 8 metals
url http://hdl.handle.net/20.500.12110/paper_1474905X_v4_n1_p75_Videla
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