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| | 1,1'-Bis(diisopropylphosphino)ferrocene Basic information | | Reaction |
| Product Name: | 1,1'-Bis(diisopropylphosphino)ferrocene | | Synonyms: | BIS[(DIISOPROPYLPHOSPHINO)CYCLOPENTADIENYL]IRON;1,1'-BIS(DIISOPROPYLPHOSPHINO)FERROCENE;-BIS(DIISOPROPYLPHOSPHINO)FERROCENE;1,1'-Bis(di-i-propylphosphino)ferrocene, min. 98%;1,1'-Bis(diisopropylphosphino)ferrocene,98%;1,1'-Bis(di-i-propylphosphino)ferrocene,min.98%;1,1'-Bis[bis(1-methylethyl)phosphino]ferrocene;Ferrocene,1,1'-bis[bis(1-Methylethyl)phosphino]- | | CAS: | 97239-80-0 | | MF: | C22H36FeP210* | | MW: | 418.31 | | EINECS: | 677-500-6 | | Product Categories: | Achiral Phosphine;Aryl Phosphine;Ligand;Ferrocenes;Metallocenes;Phosphine Ligands;Synthetic Organic Chemistry;Catalysis and Inorganic Chemistry;Phosphorus Compounds;Polydentate Phosphine Ligands | | Mol File: | 97239-80-0.mol |  |
| | 1,1'-Bis(diisopropylphosphino)ferrocene Chemical Properties |
| Melting point | 50-52 °C(lit.) | | Fp | >230 °F | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | form | Powder | | color | orange-yellow | | Water Solubility | Insoluble in water. | | InChI | InChI=1S/2C11H18P.Fe/c2*1-9(2)12(10(3)4)11-7-5-6-8-11;/h2*5-10H,1-4H3; | | InChIKey | LPBBEMRSRONKMN-UHFFFAOYSA-N | | SMILES | P(C(C)C)(C(C)C)[C]1[CH][CH][CH][CH]1.P(C(C)C)(C(C)C)[C]1[CH][CH][CH][CH]1.[Fe] |^1:7,8,9,10,11,19,20,21,22,23| | | CAS DataBase Reference | 97239-80-0(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 37/39-26 | | WGK Germany | 3 | | TSCA | No | | HS Code | 29319090 |
| | 1,1'-Bis(diisopropylphosphino)ferrocene Usage And Synthesis |
| Reaction |
- Ruthenium- catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes
- Ligand for palladium-catalyzed aminocarbonylation of Pyridyl Tosylates by means of ex situ generation of CO.
- Pd-catalyzed carbonylative ɑ-arylation of ketones with aryl iodides
- Ligand for palladium-catalyzed alkoxycarbonylation of aryl bromides for the preparation of tertiary esters
- Ligand for stereoselective palladium-catalyzed decarboxylative allylation ß-C-glycosylation
- Ligand for ruthenium-catalyzed C—C coupling reactions of fluorinated alcohols with allenes.
- Ligand for cobalt-catalyzed intermolecular formal hydroacylation reaction of olefins using N-3-picolin-2-yl aldimines as aldehyde equivalents.
 
| | Description | 1,1′-Bis(diisopropylphosphino)ferrocene (DiPPF) is a ferrocene-based phosphine ligand frequently is used in electrochemical reaction studies. DiPPF can help support high oxidation states of metal atoms by forming iron interactions and donating electrons via low-energy charge transfer from iron to nickel atoms. | | Chemical Properties | orange crystalline powder | | Uses | The general and efficient cross-coupling of thiols with aryl halides was developed utilizing Pd(OAc) 2 /1,1?-bis(diisopropylphosphino)ferrocene as the catalyst. The oxidative electrochemistry of dippf was examined, and it was found to follow an ECDim mechanism. Seven new compounds containing dippf were prepared and characterized spectroscopically. The crystal structures of [MCl2(dippf)] (M = Pt and Zn) were determined. | | reaction suitability | reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand |
| | 1,1'-Bis(diisopropylphosphino)ferrocene Preparation Products And Raw materials |
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