Rhodium(II) acetate is the
coordination compound with the
formula Rh2(AcO)
4, where AcO
− is the
acetate ion (). This dark green powder is slightly soluble in polar solvents, including water. It is used as a catalyst for
cyclopropanation
In organic chemistry, cyclopropanation refers to any chemical process which generates cyclopropane () rings. It is an important process in modern chemistry as many useful compounds bear this motif; for example pyrethroids and a number of quinolon ...
of
alkene
In organic chemistry, an alkene is a hydrocarbon containing a carbon–carbon double bond.
Alkene is often used as synonym of olefin, that is, any hydrocarbon containing one or more double bonds.H. Stephen Stoker (2015): General, Organic, an ...
s. It is a widely studied example of a
transition metal carboxylate complex.
Preparation
Rhodium(II) acetate is usually prepared by the heating of
hydrated
Drinking is the act of ingesting water or other liquids into the body through the mouth, proboscis, or elsewhere. Humans drink by swallowing, completed by peristalsis in the esophagus. The physiological processes of drinking vary widely among o ...
rhodium(III) chloride
Rhodium(III) chloride refers to inorganic compounds with the formula RhCl3(H2O)''n'', where ''n'' varies from 0 to 3. These are diamagnetic solids featuring octahedral Rh(III) centres. Depending on the value of ''n'', the material is either a den ...
in
acetic acid (CH
3COOH): Rhodium(II) acetate dimer undergoes
ligand exchange, the replacement of the acetate group by other
carboxylate
In organic chemistry, a carboxylate is the conjugate base of a carboxylic acid, (or ). It is an ion with negative charge.
Carboxylate salts are salts that have the general formula , where M is a metal and ''n'' is 1, 2,...; ''carboxylat ...
s and related groups.
:Rh
2(OAc)
4 + 4 HO
2CR → Rh
2(O
2CR)
4 + 4 HOAc
Structure and properties
The structure of rhodium(II) acetate features a pair of
rhodium
Rhodium is a chemical element with the symbol Rh and atomic number 45. It is a very rare, silvery-white, hard, corrosion-resistant transition metal. It is a noble metal and a member of the platinum group. It has only one naturally occurring i ...
atoms, each with
octahedral molecular geometry, defined by four acetate oxygen atoms, water, and a Rh–Rh bond of length 2.39
Å. The water
adduct
An adduct (from the Latin ''adductus'', "drawn toward" alternatively, a contraction of "addition product") is a product of a direct addition of two or more distinct molecules, resulting in a single reaction product containing all atoms of all co ...
is exchangeable, and a variety of other
Lewis bases bind to the axial positions.
Copper(II) acetate
Copper(II) acetate, also referred to as cupric acetate, is the chemical compound with the formula Cu(OAc)2 where AcO− is acetate (). The hydrated derivative, Cu2(OAc)4(H2O)2, which contains one molecule of water for each copper atom, is availab ...
and
chromium(II) acetate
Chromium(II) acetate hydrate, also known as chromous acetate, is the coordination compound with the formula Cr2(CH3CO2)4(H2O)2. This formula is commonly abbreviated Cr2(OAc)4(H2O)2. This red-coloured compound features a quadruple bond. The prepara ...
adopt
similar structures.
Chemical properties
The application of dirhodium tetraacetate to organic synthesis was pioneered by Teyssie and co-workers. An extensive range of reactions including insertion into bonds and the
cyclopropanation
In organic chemistry, cyclopropanation refers to any chemical process which generates cyclopropane () rings. It is an important process in modern chemistry as many useful compounds bear this motif; for example pyrethroids and a number of quinolon ...
of
alkenes
In organic chemistry, an alkene is a hydrocarbon containing a carbon–carbon double bond.
Alkene is often used as synonym of olefin, that is, any hydrocarbon containing one or more double bonds.H. Stephen Stoker (2015): General, Organic, an ...
and
aromatic
In chemistry, aromaticity is a chemical property of cyclic ( ring-shaped), ''typically'' planar (flat) molecular structures with pi bonds in resonance (those containing delocalized electrons) that gives increased stability compared to satur ...
systems. It selectively binds
ribonucleosides A ribonucleoside is a type of nucleoside including ribose as a component.
One example of a ribonucleoside is cytidine
Cytidine (symbol C or Cyd) is a nucleoside molecule that is formed when cytosine is attached to a ribose ring (also known as a ...
(vs.
deoxynucleosides
A deoxyribonucleotide is a nucleotide that contains deoxyribose. They are the monomeric units of the informational biopolymer, deoxyribonucleic acid ( DNA). Each deoxyribonucleotide comprises three parts: a deoxyribose sugar (monosaccharide), a n ...
) by binding selectively to ribonucleosides at their 2′ and 3′
–OH groups.
Rhodium(II) acetate dimer, compared to
copper(II) acetate
Copper(II) acetate, also referred to as cupric acetate, is the chemical compound with the formula Cu(OAc)2 where AcO− is acetate (). The hydrated derivative, Cu2(OAc)4(H2O)2, which contains one molecule of water for each copper atom, is availab ...
, is more reactive and useful in differentiating ribonucleosides and deoxynucleosides because it is soluble in
aqueous
An aqueous solution is a solution in which the solvent is water. It is mostly shown in chemical equations by appending (aq) to the relevant chemical formula. For example, a solution of table salt, or sodium chloride (NaCl), in water would be re ...
solution like water whereas copper(II) acetate only dissolves in non-aqueous solution.
Selected catalytic reactions
Dirhodium tetraacetate is also used as
catalyst
Catalysis () is the process of increasing the rate of a chemical reaction by adding a substance known as a catalyst (). Catalysts are not consumed in the reaction and remain unchanged after it. If the reaction is rapid and the catalyst recyc ...
for insertion into C–H and X–H bonds (X = N, S, O).
#Cyclopropanation
#:
through the
decomposition
Decomposition or rot is the process by which dead organic substances are broken down into simpler organic or inorganic matter such as carbon dioxide, water, simple sugars and mineral salts. The process is a part of the nutrient cycle and is e ...
of diazocarbonyl compounds, the intra- and intermolecular
cyclopropanation
In organic chemistry, cyclopropanation refers to any chemical process which generates cyclopropane () rings. It is an important process in modern chemistry as many useful compounds bear this motif; for example pyrethroids and a number of quinolon ...
reactions occurs.
#Aromatic cycloaddition
#:
Rhodium acetate catalyzes both two-component
cycloaddition
In organic chemistry, a cycloaddition is a chemical reaction in which "two or more unsaturated molecules (or parts of the same molecule) combine with the formation of a cyclic adduct in which there is a net reduction of the bond multiplicity". T ...
as well as three-component 1,3-dipolar cycloadditions.
#C–H insertion
#:
Rh(II)-catalyzed
regioselective
In chemistry, regioselectivity is the preference of chemical bonding or breaking in one direction over all other possible directions. It can often apply to which of many possible positions a reagent will affect, such as which proton a strong Base ( ...
intramolecular and regiospecific intermolecular
C–H insertion into
aliphatic
In organic chemistry, hydrocarbons ( compounds composed solely of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (; G. ''aleiphar'', fat, oil). Aliphatic compounds can be saturated, like hexane, ...
and
aromatic
In chemistry, aromaticity is a chemical property of cyclic ( ring-shaped), ''typically'' planar (flat) molecular structures with pi bonds in resonance (those containing delocalized electrons) that gives increased stability compared to satur ...
C–H bonds is a useful method for the synthesis of a diverse range of organic compounds.
#Oxidation of alcohols
#:
Allylic and
benzylic
In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure . Benzyl features a benzene ring () attached to a methylene group () group.
Nomenclature
In IUPAC nomenclature, the prefix benzyl refers to a subst ...
alcohols were oxidized to the corresponding carbonyl compounds using ''tert''-butyl hydroperoxide in
stoichiometric
Stoichiometry refers to the relationship between the quantities of reactants and products before, during, and following chemical reactions.
Stoichiometry is founded on the law of conservation of mass where the total mass of the reactants equ ...
amounts and Rh
2(OAc)
4 as catalyst in
dichloromethane at ambient temperature.
#X–H insertion (X = N, S, O)
#:
Rh(II)
carbenoid In chemistry a carbenoid is a reactive intermediate that shares reaction characteristics with a carbene. In the Simmons–Smith reaction the carbenoid intermediate is a zinc / iodine complex that takes the form of
:I-CH2-Zn-I
This complex reacts w ...
reacts with
amine
In chemistry, amines (, ) are compounds and functional groups that contain a basic nitrogen atom with a lone pair. Amines are formally derivatives of ammonia (), wherein one or more hydrogen
Hydrogen is the chemical element wi ...
s,
alcohols or
thiols
In organic chemistry, a thiol (; ), or thiol derivative, is any organosulfur compound of the form , where R represents an alkyl or other organic substituent. The functional group itself is referred to as either a thiol group or a sulfhydryl grou ...
to yield the product of a formal intra- or intermolecular X–H bond (X = N, S, O) insertion via the formation of an
ylide An ylide or ylid () is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached to a heteroatom with a formal positive charge (usually nitrogen, phosphorus or sulfur), and in which both atoms ...
intermediate.
References
{{DEFAULTSORT:Rhodium(II) Acetate
Rhodium compounds
Acetates
Dimers (chemistry)
Chemical compounds containing metal–metal bonds