Crystal structure and electronic and magnetic properties of hexacyanoosmate(III)
The [OsIII(CN)6]3- anion is prepared by chemical oxidation in aqueous solution and isolated as yellow prisms of [Ph 4P]3[OsIII(CN)6]·6H 2O (1). This species crystallizes in the triclinic space group P1 with cell parameters a = 13.7609(11) Å, b = 16.2275(13) Å, c = 17.0895(14) Å, α = 91.4040(10)°, β...
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todo:paper_00201669_v45_n6_p2361_Albores2023-10-03T14:16:57Z Crystal structure and electronic and magnetic properties of hexacyanoosmate(III) Albores, P. Slep, L.D. Baraldo, L.M. Baggio, R. Garland, M.T. Rentschler, E. The [OsIII(CN)6]3- anion is prepared by chemical oxidation in aqueous solution and isolated as yellow prisms of [Ph 4P]3[OsIII(CN)6]·6H 2O (1). This species crystallizes in the triclinic space group P1 with cell parameters a = 13.7609(11) Å, b = 16.2275(13) Å, c = 17.0895(14) Å, α = 91.4040(10)°, β = 109.3600(10)°, γ = 102.3970(10)°, V = 3497.4(5) Å3, and Z = 2. The slightly distorted octahedral moiety displays Os-C and C-N bond lengths that average 2.058 and 1.146 Å, respectively. Spin-orbit-coupling splitting of the ground-state term dominates the NIR region of the electronic spectrum and the magnetic behavior of 1. The experimental information points to higher spin delocalization over the coordinated cyanides than in [FeIII(CN) 6]3-. © 2006 American Chemical Society. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00201669_v45_n6_p2361_Albores |
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 [OsIII(CN)6]3- anion is prepared by chemical oxidation in aqueous solution and isolated as yellow prisms of [Ph 4P]3[OsIII(CN)6]·6H 2O (1). This species crystallizes in the triclinic space group P1 with cell parameters a = 13.7609(11) Å, b = 16.2275(13) Å, c = 17.0895(14) Å, α = 91.4040(10)°, β = 109.3600(10)°, γ = 102.3970(10)°, V = 3497.4(5) Å3, and Z = 2. The slightly distorted octahedral moiety displays Os-C and C-N bond lengths that average 2.058 and 1.146 Å, respectively. Spin-orbit-coupling splitting of the ground-state term dominates the NIR region of the electronic spectrum and the magnetic behavior of 1. The experimental information points to higher spin delocalization over the coordinated cyanides than in [FeIII(CN) 6]3-. © 2006 American Chemical Society. |
format |
JOUR |
author |
Albores, P. Slep, L.D. Baraldo, L.M. Baggio, R. Garland, M.T. Rentschler, E. |
spellingShingle |
Albores, P. Slep, L.D. Baraldo, L.M. Baggio, R. Garland, M.T. Rentschler, E. Crystal structure and electronic and magnetic properties of hexacyanoosmate(III) |
author_facet |
Albores, P. Slep, L.D. Baraldo, L.M. Baggio, R. Garland, M.T. Rentschler, E. |
author_sort |
Albores, P. |
title |
Crystal structure and electronic and magnetic properties of hexacyanoosmate(III) |
title_short |
Crystal structure and electronic and magnetic properties of hexacyanoosmate(III) |
title_full |
Crystal structure and electronic and magnetic properties of hexacyanoosmate(III) |
title_fullStr |
Crystal structure and electronic and magnetic properties of hexacyanoosmate(III) |
title_full_unstemmed |
Crystal structure and electronic and magnetic properties of hexacyanoosmate(III) |
title_sort |
crystal structure and electronic and magnetic properties of hexacyanoosmate(iii) |
url |
http://hdl.handle.net/20.500.12110/paper_00201669_v45_n6_p2361_Albores |
work_keys_str_mv |
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_version_ |
1807315792166912000 |