Tris(triphenylphosphine)rhodium(I) chloride 三(三苯基膦)氯化铑(I)

CAS 14694-95-2 MFCD00010016

化学结构图

14694-95-2
SMILES: [Cl-].[Rh].c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1

化学属性

Mol. FormulaC54H45ClP3Rh
Mol. Weight925.23
Melting Point245-250°C
SolubilitySoluble in most solvents (e.g. benzene, ethanol, chloroform, dichloromethane) but with phosphine dissociation. Reacts with O2 in solution
TSCAYes
Density1.422
Stability对光、空气、热敏感
Appearance maroon beads; 20-60 mesh maroon xtl.

别名和识别编码

Chemical NameTris(triphenylphosphine)rhodium(I) chloride
CAS Number14694-95-2
Synonym NSC 124140 RhCl(PPh3)3 Wilkinson 催化剂 三(三苯膦基)氯化铑(I) Chlorotris(triphenylphosphine) rhodium 三苯基膦氯铑 Tris(triphenylphosphine)chlororhodium(I) Tris(triphenylphosphino)chlororhodium ######## Chlorotris(triphenylphosphine)rhodium(I) 三(三苯基膦)氯化铑(I) Chlorotris(triphenylphosphine)rhodium(I); Tris(triphenylphosphine)rhodium(I) chloride; Wilkinson's catalyst 三(三苯基膦)氯化铑 tris(triphenylphosphine)rhodium (I) chloride Rhodium tris(triphenylphosphine) chloride Tris(triphenylphosphine)chlororhodium Tris(triphenylphosphine)rhodium monochloride Rhodiumtris-(triphenylphosphin)-chlorid Tris-(triphenylphosphin)-rhodium(I)-chlorid Wilkinson's catalystTris(triphenylphosphine)rhodium(I) chloride Chlorotris(triphenylphosphine)rhodium(I)Wilkinson's Catalyst 铑膦 Chlorotris(triphenylphosphin)-rhodium(I) Tris(triphenylphosphine)rhodium(I) chloride Chlorotris(triphenylphosphine)-rhodium Wilkinson's Katalysator Tris(triphenylphosphine)rhodium(I)chloride Polymer-bound chlorotris(triphenylphosphine)rhodium(I) on styrene-divinylbenzene copolymer(20% cross-linked) Chlorotris(triphenylphosphine)rhodium (I) Tris(triphenylphosphine)rhodium chloride Rhodium, chlorotris(triphenylphosphine)-, (SP-4-2)- Tris(triphenylphosphin)-rhodium(I)-chlorid Wilkinson's catalyst Chlorotris(triphenylphosphine)rhodium Wilkinson's catalyst
MDL NumberMFCD00010016
PubChem Substance ID84599
Beilstein Registry Number4581440
EC Number238-744-5
Merck Number9758
Reaxys-RN14664394
Chemical Name Translation三(三苯基膦)氯化铑(I)
InChIInChI=1S/3C18H15P.ClH.Rh/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;/h3*1-15H;1H;/p-1
LabNetwork Molecule IDLN00236013
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分类

  • Catalyst
  • Aromatics
  • {uni_hamburg} no charge; carbocycle; aromatic; 6RingOnly; 6ring; 1fragment
  • {SNA} Catalysis and Inorganic Chemistry, Chemical Synthesis, Rhodium

产品应用

  • 1. 石蜡加氢催化剂
  • 2. 在温和条件下进行催化加氢
  • 3. 醛脱羰基反应催化剂
  • 4. 丙烯的局部取代反应
  • 5. 氧化、异构化、羰基化、氢化、硅氢化等反应。

相关文献及参考

  • Electron-deficient olefins undergo Rh-catalyzed 1,4-addition with Bis(pinacolato)­diboron, L16088, e.g. 2-cyclohexen-1-one to the ß-borylcyclohexanone: Tetrahedron Lett., 43, 2323 (2002):
  • Homogeneous hydrogenation catalyst: J. Chem. Soc. (A), 1711 (1966), useful e.g. for the selective reduction of an unhindered alkene, of an unconjugated in the presence of a conjugated alkene: Org. Synth. Coll., 6, 459 (1988), or an alkene in the presence of a nitro-group: J. Org. Chem., 67, 3163 (2002). Hydroxyl groups protected as their allyl ethers may be deprotected by isomerization with Wilkinson's Catalyst to the more readily-hydrolyzed 1-propenyl ether: J. Org. Chem., 38, 3224 (1973).
  • Evans, D.A. et al.: J. Am. Chem. Soc., 110, 6917 (1988); Ojima, I. et al.: Tetrahedron Lett., 13, 5035 (1972); Birch, A.J. et al.: Org. React., 24 (1976);
  • Short: III/10b
  • Short: EINECS
  • Catalyst for hydrosilylation reactions, e.g. with Triethyl­silane, A10320, including ɑ&#
  • Catalyst for hydrosilylation reactions, e.g. with Triethyl­silane, A10320, including ɑß-unsaturated ketones to silyl enol ethers, which can be hydrolyzed to saturated ketones: Organometallics, 1, 1390 (1982), and ɑß-unsaturated esters to silyl ketene acetals with high (Z)-selectivity: Synth. Commun., 17, 1 (1989).
  • Homogeneous hydrogenation catalyst: J. Chem. Soc.(A), 1711 (1966), useful e.g. for the selective reduction of an unhindered alkene, of an unconjugated in the presence of a conjugated alkene: Org. Synth. Coll., 6, 459 (1988), or an alkene in the presence of a nitro group: J. Org. Chem., 67, 3163 (2002). Hydroxyl groups protected as their allyl ethers may be deprotected by isomerization with Wilkinson's Catalyst to the more readily-hydrolyzed 1-propenyl ether: J. Org. Chem., 38, 3224 (1973).
  • Co-catalyst giving improved results in intramolecular Heck coupling reactions catalyzed by Pd(OAc)2: J. Org. C

安全信息

WGK Germany1
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Safety Statements
  • S28 After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) 皮肤接触后,立即用大量…(由生产厂家指定)冲洗;
  • S26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 眼睛接触后,立即用大量水冲洗并征求医生意见;
  • S37/39 Wear suitable gloves and eye/face protection 穿戴适当的手套和眼睛/面保护;
  • S15 Keep away from heat 远离热源;
  • S36/37/39 Wear suitable protective clothing, gloves and eye/face protection 穿戴适当的防护服、手套和眼睛/面保护;
  • S60 This material and its container must be disposed of as hazardous waste 该物质及其容器必须作为危险废物处置;
  • S61 Avoid release to the environment. Refer to special instructions/safety data sheet 避免释放到环境中,参考特别指示/安全收据说明书;
Risk Statements
  • R36/37/38 Irritating to eyes, respiratory system and skin 对眼睛、呼吸系统和皮肤有刺激性
  • R53 May cause long-term adverse effects in the aquatic environment 对水生环境有长期的有害作用
  • R36/38 Irritating to eyes and skin 对眼睛和皮肤有刺激性
Signal word Warning
GHS Symbol
Precautionary statements
  • P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
  • P362 Take off contaminated clothing and wash before reuse. 脱掉污染的衣服,清洗后方可重新使用
  • P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
  • P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
  • P305+P351+P338
  • P332+P313
  • P305+P351+P338+P337+P313
  • P302+P350
  • P337+P313
  • P302+P352+P332+P313+P362+P364
Hazard Codes Xi
Hazard statements
  • H315 Causes skin irritation 会刺激皮肤
Storage condition 充氩储存 充氩储存。 Air Sensitive

其他信息

  • 空气中缓慢分解。不溶于水,溶于大多数溶剂,如苯、乙醇、丙酮、氯仿、二氯甲烷等,同时伴随膦的解离,溶液中会与氧发生反应。空气中缓慢分解。

系列性分类


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