Acetic acid, rhodium salt (4:2)

HCID 423677CAS 15956-28-2

기본 정보

표준 SMILES
CC(=O)O.CC(=O)O.CC(=O)O.CC(=O)O.[Rh].[Rh]
InChIKey
DRGVLUZIGUIMLB-UHFFFAOYSA-N
분자식
C8H16O8Rh2
평균 분자량
446.02 g/mol

이름 및 식별자

우선 이름
Acetic acid, rhodium salt (4:2)
IUPAC
acetic acid;bis(rhodium)
영어명
Rhodium(II) acetate dimer
분자식
C8H12O8Rh2
분자량
441.99

이름 및 동의어

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

데이터베이스 식별자

CAS
15956-28-2
PubChem CID
423677

물성

구조 계산 물성

극성 표면적
149 Ų
수소 결합 공여자 수
4
수소 결합 수용자 수
8
회전 가능 결합 수
0
무거운 원자 수
18

물리화학적 성질

녹는점
205 °C · 205 °C
저장 조건
Inert atmosphere,Room Temperature
용해도
메탄올 + 물(약간 용해됨)
물리적 상태
가루
색상
녹색에서 진한 녹색까지
수용성
수용액에 있는 가용. 에탄올에 약간 용해됨

화학적 성질

Rhodium(II) acetate dimer is Emerald Green Powder. Soluble in methanol. It is soluble in water, while the relative solubility of copper acetate in water is small.

안전 및 규제

안전 데이터

wgk
3
tsca
No
rtecs
VI9361000
HS 번호
28439000
risk_code
36/38
hazard_code
Xi

화학 및 산업

응용 분야 · 1건

용도Rhodium (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.

제조 방법 · 1건

Rhodium(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%).

공급사50 곳

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