(Cymene)ruthenium dichloride dimer

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(cymene)ruthenium dichloride dimer
RuCymCl2.png
(cymene)RuCl2 dimer.jpg
Names
Other names
Dichloro(p-cymene)ruthenium(II) dimer
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.126.850
Properties
C20H28Cl4Ru2
Molar mass 612.38 g·mol−1
Appearance Red solid
Melting point 247 to 250 °C (477 to 482 °F; 520 to 523 K) (decomposes)
Slightly, with hydrolysis
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

(Cymene)ruthenium dichloride dimer is the organometallic compound with the formula [(cymene)RuCl2]2. This red-coloured, diamagnetic solid is a reagent in organometallic chemistry and homogeneous catalysis. The complex is structurally similar to (benzene)ruthenium dichloride dimer.

Preparation and reactions[edit]

The dimer is prepared by the reaction of the phellandrene with hydrated ruthenium trichloride.[1] At high temperatures, [(cymene)RuCl2]2 exchanges with other arenes:

[(cymene)RuCl2]2 + 2 C6Me6 → [(C6Me6)RuCl2]2 + 2 cymene

(Cymene)ruthenium dichloride dimer reacts with Lewis bases to give monometallic adducts:

[(cymene)RuCl2]2 + 2 PPh3 → 2 (cymene)RuCl2(PPh3)

Such monomers adopt pseudo-octahedral piano-stool structures.

Precursor to catalysts[edit]

Treatment of [(cymene)RuCl2]2 with the chelating ligand TsDPENH gives (cymene)Ru(TsDPEN-H), a catalyst for asymmetric transfer hydrogenation.[2]

[(cymene)RuCl2]2 is also used to prepare catalysts (by monomerization with dppf) used in borrowing hydrogen catalysis,[3] a catalytic reaction that is based on the activation of alcohols towards nucleophilic attack.

References[edit]

  1. ^ Bennett, M. A.; Huang, T. N.; Matheson, T. W.; Smith, A. K. (1982). "(η6-Hexamethylbenzene)ruthenium Complexes". Inorganic Syntheses. 21: 74–78. doi:10.1002/9780470132524.ch16.
  2. ^ Takao Ikariya; Shohei Hashiguchi; Kunihiko Murata; Ryōji Noyori (2005). "Preparation of Optically Active (R,R)-Hydrobenzoin from Benzoin or Benzil". Organic Syntheses: 10.
  3. ^ Hamid et al.; Advanced Synthesis & Catalysis Volume 349, Issue 10, pages 1555–1575, July 2, 2007; doi:10.1002/adsc.200600638