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
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
- 형식 전하
- 0
- 복잡도
- 181
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
- 안정성
- 흡습성
- InChI
- InChI=1S/4C2H4O2.2Rh/c4*1-2(3)4;;/h4*1H3,(H,3,4);;/q;;;;2*+2/p-4
- InChIKey
- ANSVJOOIUURYRN-UHFFFAOYSA-N
- SMILES
- CC1=O[Rh+2]234O=C(C)[O-][Rh+2]2(O=C(C)[O-]3)(O=C(C)[O-]4)[O-]1
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
- safety_code
- 37/39-26-15
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2
- 스토리지 클래스
- 11 - Combustible Solids
화학 및 산업
응용 분야
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
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%).
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