Tetrakis[μ-(acetato-O:O')]dirhodium

Dirhodium tetraacetate

HCID 152122CAS 15956-28-2

Grundinformationen

Standard-SMILES
CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Rh+2].[Rh+2]
InChIKey
ANSVJOOIUURYRN-UHFFFAOYSA-N
Summenformel
C8H12O8Rh2
Durchschnittliche Molmasse
441,99 g/mol

Überblick

structure given in first source

Namen und Bezeichner

Bevorzugter Name
Dirhodium tetraacetate
IUPAC
bis(rhodium(2+));tetraacetate
Lokaler Name
Tetrakis[μ-(acetato-O:O')]dirhodium
Englischer Name
Rhodium(II) acetate dimer
Summenformel
C8H12O8Rh2
Molmasse
441.99

Namen und Synonyme

Dirhodium tetraacetate15956-28-2Rhodium diacetate dimerRhodium acetate, dimerTetraacetatodirhodiumTetrakis(acetato)dirhodium(II)Tetrakis(acetato)dirhodiumRh2(OAc)4NK3058Z56XRhodium(II) acetateNSC-156310DTXSID201314246
Weitere Namen anzeigen
RHODIUM ACETATE DIMERdirhodiumtetraacetatetetraacRh2(CH3CO2)4Dimer acid rhodiumRHODIUM(11) ACETATErhodiumdiacetatedimer
DRTARh2(II)(acetate)4RefChem:134894tetra-mu-acetatodirhodium(II)DTXCID501744056240-084-8Rhodium(II) acetate dimerDirhodium(II) Tetraacetate

Datenbank-Bezeichner

CAS
15956-28-2
PubChem CID
152122
UNII
NK3058Z56X
EC Number
240-084-8

Eigenschaften

Berechnete Struktureigenschaften

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

Experimentelle und physikochemische Eigenschaften

Chemical ClassesMetals -> Organic Acids, Metal Salts
Physical DescriptionGreen powder; Insoluble in water; [Alfa Aesar MSDS]

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

GHS-Klassifizierung

GHS Classification · 5 Einträge

This chemical does not meet GHS hazard criteria for 12.5% (1 of 8) of reports.

Warning

H315 (87.5%): Causes skin irritation [Warning Skin corrosion/irritation]

P264, P264+P265, P273, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, P362+P364, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 8 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Regulatory InformationDirhodium tetraacetate: Does not have an individual approval but may be used under an appropriate group standard
Hazards SummaryMay cause irritation; [Alfa Aesar MSDS] See Rhodium.
Hazard Classes and CategoriesSkin Irrit. 2 (87.5%)

Sicherheit und Schutzausrüstung

Threshold Limit Values (TLV)1.0 [mg/m3], as Rh
Permissible Exposure Limit (PEL)0.1 [mg/m3], as Rh

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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