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==Structure and synthesis==
==Structure and synthesis==
The cluster has ''D<sub>3h</sub>'' [[symmetry group|symmetry]], consisting of an [[equilateral triangle]] of Ru atoms, each of which bears two axial and two equatorial CO ligands.<ref>Slebodnick, C.; Zhao, J.; Angel, R.; Hanson, B. E.; Song, Y.; Liu, Z.; Hemley, R. J., "High Pressure Study of Ru<sub>3</sub>(CO)<sub>12</sub> by X-ray Diffraction, Raman, and Infrared Spectroscopy", Inorg. Chem., 2004, vol. 43, 5245-52. {{doi|10.1021/ic049617y }}</ref> [[triosmium dodecacarbonyl|Os<sub>3</sub>(CO)<sub>12</sub>]] has the same structure, whereas [[triiron dodecacarbonyl|Fe<sub>3</sub>(CO)<sub>12</sub>]] is different, with two bridging CO ligands, resulting in C<sub>2v</sub> symmetry.
The cluster has ''D<sub>3h</sub>'' [[symmetry group|symmetry]], consisting of an [[equilateral triangle]] of Ru atoms, each of which bears two axial and two equatorial CO ligands. The Ru-Ru distance is 284 [[picometer|pm]].<ref>{{cite journal|last1=Slebodnick|first1=C.|last2=Zhao|first2=J.|last3=Angel|first3=R.|last4=Hanson|first4=B. E.|last5=Song|first5=Y.|last6=Liu|first6=Z.|last7=Hemley|first7=R. J.|title=High Pressure Study of Ru<sub>3</sub>(CO)<sub>12</sub> by X-ray Diffraction, Raman, and Infrared Spectroscopy|journal=Inorg. Chem.|year=2004|volume= 43|page=5245-52|doi=10.1021/ic049617y }}</ref> [[triosmium dodecacarbonyl|Os<sub>3</sub>(CO)<sub>12</sub>]] has the same structure. In [[triiron dodecacarbonyl|Fe<sub>3</sub>(CO)<sub>12</sub>]], two CO ligands are [[bridging ligand|bridging]], resulting in C<sub>2v</sub> symmetry.


Ru<sub>3</sub>(CO)<sub>12</sub> is prepared by treating solutions of [[ruthenium(III) chloride|ruthenium trichloride]] with [[carbon monoxide]] in the presence of a base. [[Dichlororuthenium tricarbonyl dimer]] is an intermediate.<ref>{{cite book|last1=Bruce|first1=M. I.|last2=Jensen|first2=C. M.|last3=Jones|first3=N. L.|title=Dodecacarbonyltriruthenium, Ru<sub>3</sub>(CO)<sub>12</sub>|series=Inorganic Syntheses|year=1989|volume=26|pages=259–61|doi=10.1002/9780470132579.ch45}}</ref><ref>{{cite book|first1=Matthieu|last1=Fauré|first2=Catherine|last2=Saccavini|first3=Guy|last3=Lavigne|title=Dodecacarbonyltriruthenium|doi=10.1002/0471653683.ch3|page=110|volume=34|year=2004|series=Inorganic Syntheses}}</ref> The stoichiometry of the reaction is uncertain, one possibility being the following:
Ru<sub>3</sub>(CO)<sub>12</sub> is prepared by treating solutions of [[ruthenium(III) chloride|ruthenium trichloride]] with [[carbon monoxide]] in the presence of a base. [[Dichlororuthenium tricarbonyl dimer]] is an intermediate.<ref>{{cite book|last1=Bruce|first1=M. I.|last2=Jensen|first2=C. M.|last3=Jones|first3=N. L.|title=Dodecacarbonyltriruthenium, Ru<sub>3</sub>(CO)<sub>12</sub>|series=Inorganic Syntheses|year=1989|volume=26|pages=259–61|doi=10.1002/9780470132579.ch45}}</ref><ref>{{cite book|first1=Matthieu|last1=Fauré|first2=Catherine|last2=Saccavini|first3=Guy|last3=Lavigne|title=Dodecacarbonyltriruthenium|doi=10.1002/0471653683.ch3|page=110|volume=34|year=2004|series=Inorganic Syntheses}}</ref> The stoichiometry of the reaction is uncertain, one possibility being the following:

Revision as of 17:19, 18 April 2023

Triruthenium dodecacarbonyl
Names
IUPAC name
cyclo-tris(tetracarbonylruthenium)(3 RuRu)
Other names
Ruthenium carbonyl
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.035.701 Edit this at Wikidata
EC Number
  • 239-287-4
  • InChI=1S/12CO.3Ru/c12*1-2;;;
    Key: NQZFAUXPNWSLBI-UHFFFAOYSA-N
  • [C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[Ru].[Ru].[Ru]
Properties
C12O12Ru3
Molar mass 639.33 g/mol
Appearance orange solid
Density 2.48 g/cm3
Melting point 224 °C (435 °F; 497 K)
Boiling point sublimes in vacuum
insoluble
Solubility in organic solvents soluble
Structure
D3h cluster
0 D
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Toxic, CO Source
GHS labelling:
GHS07: Exclamation mark
Warning
H302, H315, H319, H332, H335
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
Related compounds
Related compounds
Triiron dodecacarbonyl
Triosmium dodecacarbonyl
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Triruthenium dodecacarbonyl is the chemical compound with the formula Ru3(CO)12. Classified as metal carbonyl cluster, it is a dark orange-colored solid that is soluble in nonpolar organic solvents. The compound serves as a precursor to other organoruthenium compounds.

Structure and synthesis

The cluster has D3h symmetry, consisting of an equilateral triangle of Ru atoms, each of which bears two axial and two equatorial CO ligands. The Ru-Ru distance is 284 pm.[1] Os3(CO)12 has the same structure. In Fe3(CO)12, two CO ligands are bridging, resulting in C2v symmetry.

Ru3(CO)12 is prepared by treating solutions of ruthenium trichloride with carbon monoxide in the presence of a base. Dichlororuthenium tricarbonyl dimer is an intermediate.[2][3] The stoichiometry of the reaction is uncertain, one possibility being the following:

6 RuCl3 + 33 CO + 18 CH3OH → 2 Ru3(CO)12 + 9 CO(OCH3)2 + 18 HCl

Reactions

The chemical properties of Ru3(CO)12 have been widely studied, and the cluster has been converted to hundreds of derivatives. High pressures of CO convert the cluster to the monomeric ruthenium pentacarbonyl, which reverts to the parent cluster upon standing.

Ru3(CO)12 + 3 CO ⇌ 3 Ru(CO)5 Keq = 3.3 x 10−7 mol dm−3 at room temperature

The instability of Ru(CO)5 contrasts with the robustness of the corresponding Fe(CO)5. The condensation of Ru(CO)5 into Ru3(CO)12 proceeds via initial, rate-limiting loss of CO to give the unstable, coordinatively unsaturated species Ru(CO)4. This tetracarbonyl binds Ru(CO)5, initiating the condensation.[4]

Upon warming under a pressure of hydrogen, Ru3(CO)12 converts to the tetrahedral cluster H4Ru4(CO)12.[5] Ru3(CO)12 undergoes substitution reactions with Lewis bases:

Ru3(CO)12 + n L → Ru3(CO)12-nLn + n CO (n = 1, 2, or 3)

where L is a tertiary phosphine or an isocyanide. It forms complexes with acenaphthylene.[6]

Ru3(CO)12 forms a variety of alkene complexes, some where the Ru3 core remains intact but often with fragmentation. Upon treatment with 1,5-cyclooctadiene gives the monoRu tricarbonyl derivative:[7]

Ru3(CO)12 + 3 C8H12 → 3 Ru(C8H12)(CO)3 + 3 CO

Ru-carbido clusters

At high temperatures, Ru3(CO)12 converts to a series of clusters that contain interstitial carbido ligands. These include Ru6C(CO)17 and Ru5C(CO)15. Anionic carbido clusters are also known, including [Ru5C(CO)14]2− and the bioctahedral cluster [Ru10C2(CO)24]2−.[8] Ru3(CO)12 -derived carbido compounds have been used to synthesize nanoparticles for catalysis. These particles consist of 6-7 atoms and thus are all surface, resulting in extraordinary activity.

References

  1. ^ Slebodnick, C.; Zhao, J.; Angel, R.; Hanson, B. E.; Song, Y.; Liu, Z.; Hemley, R. J. (2004). "High Pressure Study of Ru3(CO)12 by X-ray Diffraction, Raman, and Infrared Spectroscopy". Inorg. Chem. 43: 5245-52. doi:10.1021/ic049617y.
  2. ^ Bruce, M. I.; Jensen, C. M.; Jones, N. L. (1989). Dodecacarbonyltriruthenium, Ru3(CO)12. Inorganic Syntheses. Vol. 26. pp. 259–61. doi:10.1002/9780470132579.ch45.
  3. ^ Fauré, Matthieu; Saccavini, Catherine; Lavigne, Guy (2004). Dodecacarbonyltriruthenium. Inorganic Syntheses. Vol. 34. p. 110. doi:10.1002/0471653683.ch3.
  4. ^ Hastings, W. R.; Roussel, M. R.; Baird, M. C. "Mechanism of the conversion of [Ru(CO)5] into [Ru3(CO)12]" Journal of the Chemical Society, Dalton Transactions, 1990, pages 203-205. doi:10.1039/DT9900000203
  5. ^ Bruce, M. I.; Williams, M. L. "Dodecacarbonyl(tetrahydrido)tetraruthenium, Ru4(μ-H)4(CO)12" Inorganic Syntheses, 1989, volume 26, pages 262-63. ISBN 0-471-50485-8.
  6. ^ Motoyama, Yukihiro; Itonaga, Chikara; Ishida, Toshiki; Takasaki, Mikihiro; Nagashima, Hideo (2005). "Catalytic Reduction of Amides to Amines with Hydrosilanes Using a Triruthenium Cluster as the Catalyst". 82: 188. doi:10.15227/orgsyn.082.0188. {{cite journal}}: Cite journal requires |journal= (help)
  7. ^ Domingos, A. J. P.; Howell, J. A. S.; Johnson, B. F. G.; Lewis, J. (1990). "Reagents for the Synthesis of η-Diene Complexes of Tricarbonyliron and Tricarbonylruthenium". Inorg. Synth. Inorganic Syntheses. 28: 52–55. doi:10.1002/9780470132593.ch11.
  8. ^ Nicholls, J. N.; Vargas, M. D. "Carbido-Carbonyl Ruthenium Cluster Complexes" Inorganic Syntheses, 1989, volume 26, pages 280-85. doi:10.1002/9780470132579.ch49