Manganese pentacarbonyl bromide

Manganese pentacarbonyl bromide
Names
Other names
bromopentacarbonylmanganese
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.035.005
EC Number
  • 238-522-8
  • InChI=1S/5CO.BrH.Mn/c5*1-2;;/h;;;;;1H;/q;;;;;;+1/p-1
    Key: OESORJHGSXJTKX-UHFFFAOYSA-M
  • [C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[Mn].[Br-]
Properties
C5BrMnO5
Molar mass 274.892 g·mol−1
Appearance orange solid
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H302, H312, H332
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Manganese pentacarbonyl bromide is an organomanganese compound with the formula BrMn(CO)5. It is a bright orange solid that is a precursor to other manganese complexes. The compound is prepared by treatment of dimanganese decacarbonyl with bromine:[1]

Mn2(CO)10 + Br2 → 2 BrMn(CO)5

The complex undergoes substitution by a variety of donor ligands (L), e.g. to give derivatives of the type BrMn(CO)3L2.

The complex adopts an octahedral coordination geometry.[2]

Manganese pentacarbonyl bromide is a precursor to the arene complexes [(η6-arene)Mn(CO)3]+.[3]

References

  1. ^ King, R. B. (1965). Organometallic Syntheses. Volume 1 Transition-Metal Compounds. New York: Academic Press. ISBN 0-444-42607-8.
  2. ^ J. G. Hernandez; I. S. Butler; T. Friščić (214). "Multi-step and multi-component organometallic synthesis in one pot using orthogonal mechanochemical reactions". Chemical Science. 5 (9): 3576. doi:10.1039/C4SC01252F.
  3. ^ S. B. Kim, S. Lotz, S. Sun, Y. K. Chung, R. D. Pike, D. A. Sweigart "Manganese Tricarbonyl Transfer (MTT) Agents" Inorganic Syntheses, 2010, Vol. 35, 109–128. doi:10.1002/9780470651568.ch6
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