[go: up one dir, main page]

Hebrard et al., 2009 - Google Patents

Cobalt-catalyzed hydroformylation of alkenes: generation and recycling of the carbonyl species, and catalytic cycle

Hebrard et al., 2009

Document ID
2911330004568137455
Author
Hebrard F
Kalck P
Publication year
Publication venue
Chemical reviews

External Links

Snippet

In1938, whileOttoRoelenwasstudyingtheFischer-Tropsch reaction, which converts H2/CO into alkanes and alkenes, and was trying to improve the yields by recycling ethylene, the cobalt catalyst deposited on a ThO2/SiO2 support produced some propanal. Fortunately …
Continue reading at pubs.acs.org (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201Oxygen-containing compounds
    • B01J31/0204Ethers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/60Reduction reactions, e.g. hydrogenation
    • B01J2231/64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/40Regeneration or reactivation
    • B01J31/4015Regeneration or reactivation of catalysts containing metals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F17/00Metallocenes
    • C07F17/02Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32Addition reactions to C=C or C-C triple bonds
    • B01J2231/321Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System

Similar Documents

Publication Publication Date Title
Hebrard et al. Cobalt-catalyzed hydroformylation of alkenes: generation and recycling of the carbonyl species, and catalytic cycle
Marinkovic et al. Fifteen years of supported ionic liquid phase-catalyzed hydroformylation: material and process developments
Hagen Industrial catalysis: a practical approach
Vilches-Herrera et al. Isomerization–hydroformylation tandem reactions
Riisager et al. Stability and kinetic studies of supported ionic liquid phase catalysts for hydroformylation of propene
Haumann et al. Hydroformylation in room temperature ionic liquids (RTILs): catalyst and process developments
Huang et al. Insights into the bimetallic effects of a RhCo catalyst for ethene hydroformylation: experimental and DFT investigations
Rodrigues et al. Reusable catalysts for hydroformylation‐based reactions
JP6077590B2 (en) Method of hydroformylation
Künnemann et al. Continuous hydroformylation of 1-decene in an aqueous biphasic system enabled by methylated cyclodextrins
JP2016135794A (en) Relaxation of fouling in hydroformylation by addition of water.
Liu et al. Unmodified rhodium-catalyzed hydroformylation of alkenes using tetrarhodium dodecacarbonyl. The infrared characterization of 15 acyl rhodium tetracarbonyl intermediates
Nair et al. Kinetics of hydroformylation of styrene using homogeneous rhodium complex catalyst
Kubis et al. Investigation into the equilibrium of iridium catalysts for the hydroformylation of olefins by combining in situ high-pressure FTIR and NMR spectroscopy
Takahashi et al. Mechanistic investigations of the ruthenium-catalyzed synthesis of acrylate salt from ethylene and CO2
Kokkinos et al. Two-step conversion of LLCN olefins to strong anti-knocking alcohol mixtures catalysed by Rh, Ru/TPPTS complexes in aqueous media
Ma et al. Hydrocarboxylation of olefins catalyzed by polyoxometalate-anchored palladium single-atom catalysts
Wang et al. A single-atom Pd catalyst anchored on a porous organic polymer for highly efficient telomerization of 1, 3-butadiene with methanol
Kokkinos et al. A potential refinery process of light–light naphtha olefins conversion to valuable oxygenated products in aqueous media–Part 1: Biphasic hydroformylation
JP5493497B2 (en) Method for producing alcohol
Phillips et al. A new class of rhodium (I) κ1-P and κ2-P, N complexes with rigid PTN (R) ligands (PTN= 7-phospha-3-methyl-1, 3, 5-triazabicyclo [3.3. 1] nonane)
Ungváry Application of transition metals in hydroformylation. Annual survey covering the year 2000
Potier et al. Cyclodextrins as first and second sphere ligands for Rh (I) complexes of lower-rim PTA derivatives for use as catalysts in aqueous phase hydrogenation
Baricelli et al. Synthesis and characterization of [HRu (CO)(CH3CN)(TPPTS) 3] BF4: Catalytic properties in the aqueous-biphasic hydroformylation of olefins
Mirbach et al. Photochemical hydroformylation of olefins with cobalt catalysts. 1. Neutral cobalt carbonyls