Dimanganese decacarbonyl

Dimanganese decacarbonyl

Names
IUPAC name bis(pentacarbonylmanganese)(Mn—Mn)
Other names Manganese carbonyl Decacarbonyldimanganese
Identifiers
CAS Number	10170-69-1 Y
3D model ( JSmol )	Interactive image
ChemSpider	451751 Y
ECHA InfoCard	100.030.392
EC Number	233-445-6
PubChem CID	517769
UNII	85SI7K7FWW Y
CompTox Dashboard (EPA)	DTXSID50895049
InChI InChI=1S/10CO.2Mn/c10*1-2;; Y Key: QFEOTYVTTQCYAZ-UHFFFAOYSA-N Y InChI=1/10CO.2Mn/c10*1-2;; Key: QFEOTYVTTQCYAZ-UHFFFAOYAD
SMILES O=C=[Mn](=C=O)(=C=O)(=C=O)(=C=O)[Mn](=C=O)(=C=O)(=C=O)(=C=O)=C=O
Properties
Chemical formula	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
Solubility in water	Insoluble
Structure[1]
Crystal structure	monoclinic
Lattice constant	a = 14.14 Å, b = 7.10 Å, c = 14.63 Å α = 90°, β = 105.2°, γ = 90°
Formula units (Z)	4
Dipole moment	0 D
Hazards
Occupational safety and health (OHS/OSH):
Main hazards	CO source
GHS labelling:[2]
Pictograms
Signal word	Danger
Hazard statements	H301, H311, H331
Precautionary statements	P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P311, P312, P321, P322, P330, P361, P363, P403+P233, P405, P501
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 verify (what is YN ?) Infobox references

Dimanganese decacarbonyl,^[3] which has the chemical formula Mn₂(CO)₁₀, is a binary bimetallic carbonyl complex centered around the first row transition metal manganese. The first reported synthesis of Mn₂(CO)₁₀ was in 1954 at Linde Air Products Company and was performed by Brimm, Lynch, and Sesny.^[4] Their hypothesis about, and synthesis of, dimanganese decacarbonyl was fundamentally guided by the previously known dirhenium decacarbonyl (Re₂(CO)₁₀), the heavy atom analogue of Mn₂(CO)₁₀. Since its first synthesis, Mn₂(CO)₁₀ has been use sparingly as a reagent in the synthesis of other chemical species, but has found the most use as a simple system on which to study fundamental chemical and physical phenomena, most notably, the metal-metal bond. Dimanganese decacarbonyl is also used as a classic example to reinforce fundamental topics in organometallic chemistry like d-electron count, the 18-electron rule, oxidation state, valency,^[5] and the isolobal analogy.

Synthesis

Many procedures have been reported for the synthesis of Mn₂(CO)₁₀ since 1954, the two most common general types are discussed herein. Some of these methods were not designed to create Mn₂(CO)₁₀, but rather treat Mn(I), Mn(II), or Mn(-I) as an oxidizing or reducing agent, respectively, for other species in the reaction, but produce Mn₂(CO)₁₀ nonetheless.

Reduction/carbonylation syntheses

The carbonylation route involves the reduction of a Mn(I) or Mn(II) salt to the Mn(0) species in concert with carbonylation to a coordinatively saturated metal center with CO gas. The carbonylation using CO can be under heightened pressures of CO, relative to atmospheric pressure, or at ambient pressure. Examples of each are given.

High pressure carbonylation

As previously mentioned, Mn₂(CO)₁₀ was first prepared in 1954 by Brimm, Lynch, and Sesny, albeit in yields of ~1%, by the reduction of manganese(II) iodide with magnesium(0) under 3000 psi (~200 atm) of carbon monoxide (CO).^[4] The balanced reaction is represented by:

A more efficient preparation was developed in 1958 and entails reduction of anhydrous manganese(II) chloride with sodium benzophenone ketyl radical under similarly high pressures (200 atm) of CO.^[6] This method yielded ~32% of the dimanganese decacarbonyl complex, producing enough material for the first real opportunities to rigorously study the chemical and physical properties of the molecule. This method is represented by the balanced equation:

Low pressure carbonylation

Despite successes in the synthesis of Mn₂(CO)₁₀, the safety concerns and limited batch size surrounding high pressure carbonylation methods necessitated alternative, low pressure procedures to obtain the target compound. In 1968, the first ambient CO pressure carbonylation synthesis of Mn₂(CO)₁₀ was reported from the commercially available and inexpensive methylcyclopentadienyl manganese tricarbonyl (MMT) and sodium(0) as the reductant.^[7] The balanced equation being:

The efficiency of the method ranged from 16 to 20% yield, lower than what was previously reported, however, it could be performed more safely and on mole scale.

Dimerization syntheses

The second overarching method used to make Mn₂(CO)₁₀ is similar to the first in that it usually requires alteration of a Mn(I), or in this case, Mn(-I) to the corresponding Mn(0) species. These preparations differ, however, by beginning with manganese precursors, sometimes commercially available, that need no additional CO ligands and simply

to form the target molecule. This poses the significant logistic and safety advantage of not dealing with toxic CO gas and is the prevailing general method for the academic synthesis of Mn₂(CO)₁₀.

The first explicit success in this area was published in 1977, which featured a pentacarbonylhydridomanganese(I) Mn source, with Se(PF₂)₂ as the reductant.^[8] The balanced equation for this transformation is:

Alterations of the terminal reductant have been reported in the manganese hydride case.^[9][10][11] Similar methods exist for Mn(CO)₅X compounds where X = Cl, Br, or I, and more rarely, Mn(CO)₆ bound with a weakly coordinating anion.^{[12][13][14][15][16][17]} Using similar logic, stable salts of the pentacarbonyl manganate anion can also be employed with an oxidant to access the same Mn₂(CO)₁₀ complex.^[18][19][20] An example of this is the reduction of triphenylcyclopropenium tetrafluoroborate with sodium pentacarbonyl manganate to produce the dimer of each.^[21] The balanced equation is given by:

One additional interesting synthesis of Mn₂(CO)₁₀ occurs by combination of a hexacarbonylmanganese(I) tetrafluoroborate salt with a sodium pentacarbonyl manganate salt. In this instance, manganese is both the oxidant and reductant, producing two formal Mn(0) atoms.^[22] The balanced equation is:

Structure and bonding

High precision

and organometallic chemistry.

The stoichiometric composition of Mn₂(CO)₁₀, derived from elemental analysis, informs a 5:1 ratio of CO to Mn. The assumed binary carbonyl complex given this information is pentacarbonylmanganese(0). However, the sum of the d-electron count (7 for Mn(0)) and the electron contributions from the ligands (10 for 5 CO) yields a 17-electron, metalloradical complex for Mn(CO)₅. This is a highly unstable configuration, isolobal to the methyl radical, which can be expected to homodimerize to the constitutionally symmetric dinuclear complex in order for both Mn nuclei to achieve an 18-electron, noble gas configuration. Indeed, the true structure of the Mn(0) binary carbonyl structure is a dimeric, dinuclear complex.

Crystal structure

This hypothesized structure was confirmed explicitly through

.

Electronic structure

Initial fundamental experimental and theoretical studies on the electronic structure of Mn₂(CO)₁₀ were performed used a mixture of photoelectron spectroscopy, infrared spectroscopy, and an iterative extended-Hückel-type molecular orbital calculation.^[27][28] The electronic structure of Mn₂(CO)₁₀ was most reported in 2017 using the BP86D functional with TZP basis set.^[29] The electronic structure described herein, along with relevant orbital plots, are reproduced from the methods used in that study using Orca (5.0.3)^[30] and visualized using IBOView (v20150427).^[31] The two main interactions of interest in the system are the metal-to-ligand pi-backbonding interactions and the metal-metal sigma bonding orbital. The pi-backbonding interactions illustrated below occur between the t_2g d-orbital set and the CO π* antibonding orbitals. The degenerate d_xz and d_yz backbonding interactions with both axial and equitorial CO ligands is the HOMO-15. More total delocalization occurs onto the axial CO antibonding orbital than does the equatorial, which is thought to rationalize the shorter Mn-C bond length.

• Two degenerate pi-backbonding orbitals of dimanganese decacarbonyl
• 
• 

The primary Mn-Mn σ-bonding orbital is composed of two d_z2 orbitals, represented by the HOMO-9.

Other large contributions made in this area were by Ahmed Zewail using ultrafast, femtosecond spectroscopy en route to his 1999 Nobel Prize.^[32] His discoveries elucidated much about the time scales and energies associated with the molecular motions of Mn₂(CO)₁₀, as well as the Mn-Mn and Mn-C bond cleavage events.^[33]

Reactivity

Mn₂(CO)₁₀ is air stable as a crystalline solid, but solutions require Schlenk techniques. Mn₂(CO)₁₀ is chemically active at both the Mn-Mn and Mn-CO bonds due to low, and surprisingly similar, bond dissociation energies of ~36 kcal/mol (151 kJ/mol)^[34] and ~38 kcal/mol (160 kJ/mol),^[35] respectively. For this reason, reactivity can happen at either site of the molecule, sometimes selectively. Examples of each are given.

Mn-Mn bond cleavage reactions

The Mn-Mn bond is sensitive to both oxidation and reduction, producing two equivalents of the corresponding Mn(I) and Mn(-I) species, respectively. Both of the potential resultant species can be derived further. Redox neutral cleavage is possible both thermally and photochemically, producing two equivalents of the Mn(0) radical. Examples of each are given below.

Oxidative cleavage

Selective mono-oxidation of the Mn-Mn bond is most often done via addition of classical metal oxidants (e.g. Ce^IV, Pb^IV, etc) or weak homonuclear single covalent bonds of the form X-X (X is group 16 or 17 element).^{[36][37][38][39][40]} These reactions yield the [Mn(CO)₅]⁺ cation with a bound weakly coordinating anion, or the Mn(CO)₅X complex. The general reaction schemes for each are seen as balanced equations below:

or for two-electron oxidantsandfor E = O, S, Se, Tefor X = F, Cl, Br, I

Reductive cleavage

Reductive cleavage is almost always done with sodium metal,^[41][42] yielding the [Mn(CO)₅]⁻ anion with the sodium counterion. The balanced general reactions are given below:

The resultant manganate anion is a potent nucleophile, which can be protonated to give the manganese hydride,^[43][44] or alkylated with organic halides^[45][46][43] to give a large swath of organomanganese(I) complexes.

Redox-neutral cleavage

Homolytic cleavage, usually via light,^[47] but sometimes heat,^[48] gives the Mn(0) metalloradical, which can react with itself to reform Mn₂(CO)₁₀, or combine with other radical species that usually result in formal oxidation to Mn(I). This reactivity is comparable to that of organic, carbon-based radicals via the isolobal analogy. The homolytic cleavage is given by:

The use of the produced radical species, [Mn(CO)₅]*, has found several applications as a radical initiator for various organic methodologies^[49][50][51] and polymerization reactions.^[52][53][54]

Ligand substitution reactions

Ligand substitution reactions that do not disrupt the Mn-Mn bonding is done by using strongly sigma donating L-type ligands that can outcompete CO without participating in redox reactivity.^[55] This requirement usually necessitates phosphines^[56][57] or N-heterocyclic carbenes (NHCs),^[58] with substitution occurring at the axial position according to the reactions below:

Safety

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

References