Olefin epoxidation and alkane hydroxylation catalyzed by robust sulfonated manganese and iron porphyrins supported on cationic ion-exchange resins
- CNRS, Toulouse (France)
Robust sulfonated manganese and iron porphyrin supported on poly(vinylpyridinium) polymers have been used as catalysts in olefin epoxidation and alkane hydroxylation by iodosylbenzene. The metalloporphyrins are attached to protonated or methylated poly(vinylpyridine) polymers by the coordination of one pyridine unit, thus providing a proximal effect, and by additional interactions of the porphyrin sulfonato groups with the polymer pyridinium units. The best catalysts are the complexes containing halogen atoms at the pyrrole [beta]-positions. In all these oxygenation reactions manganese porphyrins are better catalysts than the corresponding iron complexes. From comparative studies with another ion-exchange resin without a potential axial ligand, it can be noted that the concept of the proximal effect is a key factor in metalloporphyrin-catalyzed reactions, not only for soluble complexes but also for supported catalysts.
- OSTI ID:
- 7180610
- Journal Information:
- Inorganic Chemistry; (United States), Journal Name: Inorganic Chemistry; (United States) Vol. 31:11; ISSN 0020-1669; ISSN INOCAJ
- Country of Publication:
- United States
- Language:
- English
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37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
ALKANES
ALKENES
CARBOXYLIC ACIDS
CATALYTIC EFFECTS
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
COMPLEXES
CYCLOALKENES
CYTOCHROMES
EPOXIDES
HETEROCYCLIC ACIDS
HETEROCYCLIC COMPOUNDS
HYDROCARBONS
HYDROXYLATION
ION EXCHANGE MATERIALS
IRON COMPLEXES
KINETICS
LIGANDS
MANGANESE COMPLEXES
MATERIALS
MOLECULAR STRUCTURE
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
OXIDATION
PIGMENTS
POLYMERS
PORPHYRINS
PROTEINS
REACTION KINETICS
SULFONATES
TRANSITION ELEMENT COMPLEXES