Tetrakis[μ-(acetato-O:O')]dirhodium

Acetic acid, rhodium salt (4:2)

HCID 423677CAS 15956-28-2

Grundinformationen

Standard-SMILES
CC(=O)O.CC(=O)O.CC(=O)O.CC(=O)O.[Rh].[Rh]
InChIKey
DRGVLUZIGUIMLB-UHFFFAOYSA-N
Summenformel
C8H16O8Rh2
Durchschnittliche Molmasse
446,02 g/mol

Namen und Bezeichner

Bevorzugter Name
Acetic acid, rhodium salt (4:2)
IUPAC
acetic acid;bis(rhodium)
Lokaler Name
Tetrakis[μ-(acetato-O:O')]dirhodium
Englischer Name
Rhodium(II) acetate dimer
Summenformel
C8H12O8Rh2
Molmasse
441.99

Namen und Synonyme

Acetic acid, rhodium salt (4:2)NSC156310Rh2(OAc)4RHODIUM ACETATE DIMERDIRHODIUM(II) TETRAACETATEdirhodiumtetraacetatetetrakis(acetato)dirhodiumtetraacRh2(CH3CO2)4Dimer acid rhodiumRHODIUM(11) ACETATErhodiumdiacetatedimer

Datenbank-Bezeichner

CAS
15956-28-2
PubChem CID
423677

Eigenschaften

Berechnete Struktureigenschaften

Polarare Oberfläche (TPSA)
149 Ų
H-Brücken-Donoren
4
H-Brücken-Akzeptoren
8
Frei drehbare Bindungen
0
Schwere Atome
18

Physikochemische Eigenschaften

Schmelzpunkt
205 °C · 205 °C
storage temp.
Inert atmosphere,Room Temperature
Löslichkeit
Methanol + Water (Slightly)
Aggregatzustand
powder
Farbe
Green to dark green
Wasserlöslichkeit
Soluble in aqueous solution like water. Slightly soluble in ethanol

Sicherheit und Regulatorisches

Sicherheitsdaten

wgk
3
tsca
No
hs_code
28439000
RTECS-Nr.
VI9361000
risk_code
36/38
hazard_code
Xi

Chemie und Industrie

Anwendungen · 1 Eintrag

VerwendenRhodium (II) Acetate Dimer is a effective catalyst for ylide formation and it is also catalyst for cyclopropanation of alkenes, oxidation of alcohols, cyclization reactions involving -diazo carbonyl groups, insertion into C-H and X-H bonds (X-H is NH or SH or OH). More reactive and useful in differentiating ribonucleosides and deoxynucleosides. It is also used in functionalizing fullerenes into polymers. Efficient catalyst for hydrogen transfer from 2-propanol to cyclohexanone and other unsaturated compounds.

Darstellung · 1 Eintrag

synthetischeRhodium(II) acetate dimer synthesis: A suspension of 10.0g. of Rh(OH)3.H20 in 400 ml. of glacial acetic acid dissolved upon refluxing for 18 hr. to give a deep emerald-green solution. Most of the acetic acid was evaporated on a steam bath; remaining traces mere removed by heating the residue at 120° for 1hr. The residue was then extracted with boiling acetone until the extract was colorless rather than bluish green. The extract was quickly passed through a fritted glass filter, concentrated on a steam bath to 1/3 its original volume, and placed in the freezing compartment of a refrigerator for 18hr. The resulting large dark green crystals were collected on a filter, washed with small portions of ice-cold acetone, and dried at 110°. When first collected, the product is the weak adduct [Rh(OOCCH3)2(CH3)2C0]2; however, acetone is lost fairly readily at room temperature and immediately in the drying oven; yield, 6.2g. (48%).

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