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  2. Rhodium - Wikipedia

    en.wikipedia.org/wiki/Rhodium

    Heating a methanolic solution of hydrated rhodium trichloride with sodium acetate give the blue-green rhodium(II) acetate, Rh 2 (O 2 CCH 3) 4, which features a Rh-Rh bond. This complex and related rhodium(II) trifluoroacetate have attracted attention as catalysts for cyclopropanation reactions.

  3. Pentamethylcyclopentadienyl rhodium dichloride dimer

    en.wikipedia.org/wiki/Pentamethylcyclopentadieny...

    This complex was first prepared from hexamethyl Dewar benzene and RhCl 3 (H 2 O) 3. [3] [4] [5] The hydrohalic acid necessary for the ring-contraction rearrangement is generated in situ in methanolic solutions of the rhodium salt, and the second step has been carried out separately, confirming this mechanistic description. [6]

  4. Chlorobis (ethylene)rhodium dimer - Wikipedia

    en.wikipedia.org/wiki/Chlorobis(ethylene)rhodium...

    Chlorobis(ethylene)rhodium dimer is an organorhodium compound with the formula Rh 2 Cl 2 (C 2 H 4) 4. It is a red-orange solid that is soluble in nonpolar organic solvents. The molecule consists of two bridging chloride ligands and four ethylene ligands. The ethylene ligands are labile and readily displaced even by other alkenes.

  5. Organorhodium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organorhodium_chemistry

    Organorhodium chemistry is the chemistry of organometallic compounds containing a rhodium-carbon chemical bond, and the study of rhodium and rhodium compounds as catalysts in organic reactions. [ 1 ] Stable organorhodium compounds and transient organorhodium intermediates are used as catalyst such as in olefin hydroformylation , olefin ...

  6. Wilkinson's catalyst - Wikipedia

    en.wikipedia.org/wiki/Wilkinson's_catalyst

    Wilkinson's catalyst (chlorido­tris(triphenylphosphine)­rhodium(I)) is a coordination complex of rhodium with the formula [RhCl(PPh 3)], where 'Ph' denotes a phenyl group. It is a red-brown colored solid that is soluble in hydrocarbon solvents such as benzene, and more so in tetrahydrofuran or chlorinated solvents such as dichloromethane .

  7. Rhodium (III) chloride - Wikipedia

    en.wikipedia.org/wiki/Rhodium(III)_chloride

    Thus, ethanolic solutions of hydrated rhodium trichloride react with diethyl sulfide: [11] "RhCl 3 (H 2 O) 3" + 3 S(C 2 H 5) 2 → RhCl 3 (S(C 2 H 5) 2) 3 + 3H 2 O. This complex has been used as source of anhydrous rhodium trichloride that is soluble in lipophilic solvents. Both fac and mer stereoisomers of such complexes have been isolated. [3]

  8. Rhodocene - Wikipedia

    en.wikipedia.org/wiki/Rhodocene

    Cotton and Wilkinson demonstrated [11] that the 18-valence electron rhodium(III) rhodocenium cation [Rh(η 5-C 5 H 5) 2] + can be reduced in aqueous solution to the monomeric form; they were unable to isolate the neutral product as not only can it dimerise, the rhodium(II) radical monomer can also spontaneously form the mixed-hapticity stable ...

  9. Tetrarhodium dodecacarbonyl - Wikipedia

    en.wikipedia.org/wiki/Tetrarhodium_dodecacarbonyl

    Because of their relevance to hydroformylation catalysis, rhodium carbonyls have been systematically studied to a high degree. The instability of Rh 2 (CO) 8 has been a source of curiosity. The analogous binary carbonyl of cobalt, Co 2 (CO) 8, is well known. Solutions of Rh 4 (CO) 12 under high pressures of CO convert to the dirhodium compound: [5]