Dimanganese decacarbonyl

From Wikipedia, the free encyclopedia

[1]

Dimanganese decacarbonyl
Dimanganese decacarbonyl
Dimanganese-decacarbonyl-3D-balls.png
Names
IUPAC name
bis(pentacarbonylmanganese)(Mn—Mn)
Other names
Manganese carbonyl
Decacarbonyldimanganese
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.392 Edit this at Wikidata
UNII
Properties
Mn2(CO)10
Molar mass 389.98 g/mol
Appearance Yellow crystals
Density 1.750 g/cm3
Melting point 154 °C (309 °F; 427 K)
Boiling point sublimes 60 °C (140 °F; 333 K) at 0.5 mm Hg
Insoluble
Structure[1]
monoclinic
a = 14.14 Å, b = 7.10 Å, c = 14.63 Å
α = 90°, β = 105.2°, γ = 90°
4
Dipole moment
 0 D
Hazards
Main hazards CO source
R-phrases (outdated) 23/24/25
S-phrases (outdated) 22-26-36/37/39-45
Related compounds
Related compounds
 Re2(CO)10
Co2(CO)8
Fe3(CO)12
Fe2(CO)9
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N  (what is checkY☒N ?)
Infobox references

Dimanganese decacarbonyl is the chemical compound with the formula Mn2(CO)10. This metal carbonyl is an important reagent in the organometallic chemistry of manganese.[2]

Synthesis[]

The compound was first prepared in low yield by the reduction of manganese iodide with magnesium under CO.[3] A more efficient preparation entails reduction of anhydrous MnCl2 with sodium benzophenone ketyl under 200 atmospheres of CO.[4] The availability of inexpensive methylcyclopentadienyl manganese tricarbonyl ("MMT") has led to a low pressure route to Mn2(CO)10.[5]

Structure[]

The crystal structure of Mn2(CO)10 was redetermined at high precision at room temperature in 1981[1] and bond lengths mentioned herein refer to results from that study. Mn2(CO)10 has no bridging CO ligands: it can be described as containing two axially-linked (CO)5Mn- subunits. There are two kinds of CO ligands; there is one CO linked to each Mn atom that is coaxial with the Mn-Mn bond and there are four “equatorial” carbonyls bonded to each Mn atom that are nearly perpendicular to the Mn-Mn bond (Mn’-Mn-CO(equatorial) angles range from 84.61(7) to 89.16(7) degrees). The axial carbonyl distance of (181.1 pm) is 4.5 pm shorter than the average equatorial manganese-carbonyl distance of 185.6 pm. In the stable rotamer, the two Mn(CO)5 subunits are staggered. Thus, the overall molecule has approximate point group D4d symmetry, which is an uncommon symmetry shared with S2F10.[6] The Mn2(CO)10 molecule is isomorphous with Re2(CO)10 and the corresponding decacarbonyl of Tc.

Reactions[]

Mn2(CO)10 is air stable as a crystalline solid, but solutions require Schlenk techniques. It finds limited use in organic synthesis.[7] Characteristic reactions:

  • Reduction of Mn2(CO)10 gives the manganese pentacarbonyl anion, which can be isolated as a salt:
Mn2(CO)10 + 2 Na → 2 Na[Mn(CO)5]

The anion is a versatile nucleophile. Protonation gives the hydride [HMn(CO)5], and methylation gives [(CH3)Mn(CO)5].

Mn2(CO)10 + Br2 → 2[Mn(CO)5Br]
  • Homolysis of Mn2(CO)10 by either heat or light gives the ·Mn(CO)5 radical, allowing Mn2(CO)10 to be used as an initiator for various polymerization reactions.[7]

Safety[]

Mn2(CO)10 is a volatile source of a metal and a source of CO.

References[]

  1. ^ Jump up to: a b c Melvyn Rowen Churchill, Kwame N. Amoh, and Harvey J. Wasserman. "Redetermination of the crystal structure of dimanganese decacarbonyl and determination of the crystal structure of dirhenium decacarbonyl. Revised values for the manganese-manganese and rhenium-rhenium bond lengths in dimanganese decacarbonyl and dirhenium decacarbonyl". Inorg. Chem. 20 (5): 1609–1611. doi:10.1021/ic50219a056.CS1 maint: multiple names: authors list (link)
  2. ^ Elschenbroich, C. "Organometallics" (2006) Wiley-VCH: Weinheim. ISBN 978-3-527-29390-2
  3. ^ Brimm, E. O.; Lynch, M. A.; Sesny, W. J. "Preparation and Properties of Manganese Carbonyl" Journal of the American Chemical Society 1954, volume 76, page 3831 - 3835.
  4. ^ King, R. B. Organometallic Syntheses. Volume 1 Transition-Metal Compounds; Academic Press: New York, 1965. ISBN 0-444-42607-8
  5. ^ King, R. B.; Stokes, J. C.; Korenowski, T. F. "A Convenient Synthesis of Dimanganese Decarbonyl from Inexpensive Starting Materials at Atmospheric Pressure" Journal of Organometallic Chemistry 1968, volume 11, Pages 641-643.
  6. ^ L. F. Dahl, E. Ishishi, R. E. Rundle "Polynuclear Metal Carbonyls. I. Structures of Mn2(CO)10 and Re2(CO)10 J. Chem. Phys. 1957, volume 26, p. 1750. doi:10.1063/1.1743615
  7. ^ Jump up to: a b Pauson, P. L. "Decacarbonyldimanganese" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289X.rd001.pub2.
Retrieved from ""