Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions

The electronic spectra of a series of [Ru(CN)<inf>5</inf>L]n- complexes (L = H<inf>2</inf>O, NH<inf>3</inf>, pyrazine, dimethyl sulphoxide, or CN-) have been measured in aqueous solution. The d-d bands were assigned on the basis of a ligand-field model for tetrago...

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Autores principales: Olabe, J.A., Zerga, H.O., Gentil, L.A.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_14727773_v_n5_p1267_Olabe
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spelling todo:paper_14727773_v_n5_p1267_Olabe2023-10-03T16:17:58Z Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions Olabe, J.A. Zerga, H.O. Gentil, L.A. The electronic spectra of a series of [Ru(CN)<inf>5</inf>L]n- complexes (L = H<inf>2</inf>O, NH<inf>3</inf>, pyrazine, dimethyl sulphoxide, or CN-) have been measured in aqueous solution. The d-d bands were assigned on the basis of a ligand-field model for tetragonally distorted octahedra and the energy of the transitions, which depends on the nature of L, were found to correlate with the rate constant for the dissociation of L from [Ru(CN)<inf>5</inf>L]n-, k<inf>-L</inf>. Comparisons are made with the similar [Fe(CN)<inf>5</inf>L]n- series. A new value of 10Dq, 4.2 μm-1, is proposed for [Ru(CN)<inf>6</inf>]4-, which is significantly higher than that corresponding to [Fe(CN)<inf>6</inf>]4-, as expected from ligand-field theory. Fil:Olabe, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_14727773_v_n5_p1267_Olabe
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description The electronic spectra of a series of [Ru(CN)<inf>5</inf>L]n- complexes (L = H<inf>2</inf>O, NH<inf>3</inf>, pyrazine, dimethyl sulphoxide, or CN-) have been measured in aqueous solution. The d-d bands were assigned on the basis of a ligand-field model for tetragonally distorted octahedra and the energy of the transitions, which depends on the nature of L, were found to correlate with the rate constant for the dissociation of L from [Ru(CN)<inf>5</inf>L]n-, k<inf>-L</inf>. Comparisons are made with the similar [Fe(CN)<inf>5</inf>L]n- series. A new value of 10Dq, 4.2 μm-1, is proposed for [Ru(CN)<inf>6</inf>]4-, which is significantly higher than that corresponding to [Fe(CN)<inf>6</inf>]4-, as expected from ligand-field theory.
format JOUR
author Olabe, J.A.
Zerga, H.O.
Gentil, L.A.
spellingShingle Olabe, J.A.
Zerga, H.O.
Gentil, L.A.
Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions
author_facet Olabe, J.A.
Zerga, H.O.
Gentil, L.A.
author_sort Olabe, J.A.
title Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions
title_short Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions
title_full Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions
title_fullStr Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions
title_full_unstemmed Electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(II) ions
title_sort electronic d-d spectra and ligand-dissociation rates of pentacyanoruthenate(ii) ions
url http://hdl.handle.net/20.500.12110/paper_14727773_v_n5_p1267_Olabe
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