Mizuno et al., 2011 - Google Patents
Molecular design of polyoxometalate-based compounds for environmentally-friendly functional group transformations: From molecular catalysts to heterogeneous …Mizuno et al., 2011
- Document ID
- 11400757959163262569
- Author
- Mizuno N
- Yamaguchi K
- Kamata K
- Publication year
- Publication venue
- Catalysis surveys from Asia
External Links
Snippet
This review article summarizes our recent researches for molecular design of polyoxometalates (POMs) and their related compounds for environmentally-friendly functional group transformations. The divacant POM [γ-SiW10O34 (H2O) 2] 4− exhibits high …
- 239000003054 catalyst 0 title abstract description 35
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts 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
- B01J31/1805—Catalysts 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0201—Oxygen-containing compounds
- B01J31/0204—Ethers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
- B01J2531/64—Molybdenum
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/06—Cobalt compounds
- C07F15/065—Cobalt compounds without a metal-carbon linkage
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/122—Metal aryl or alkyl compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0213—Complexes without C-metal linkages
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/70—Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Mizuno et al. | Molecular design of polyoxometalate-based compounds for environmentally-friendly functional group transformations: From molecular catalysts to heterogeneous catalysts | |
Mizuno et al. | Green oxidation reactions by polyoxometalate-based catalysts: from molecular to solid catalysts | |
Ma et al. | Identifying catalytically active mononuclear peroxoniobate anion of ionic liquids in the epoxidation of olefins | |
Miceli et al. | Vanadium (V) catalysts with high activity for the coupling of epoxides and CO2: characterization of a putative catalytic intermediate | |
Bania et al. | Enhanced catalytic activity of zeolite encapsulated Fe (III)-Schiff-base complexes for oxidative coupling of 2-napthol | |
Zhang et al. | A new layered metal–organic framework as a promising heterogeneous catalyst for olefin epoxidation reactions | |
Ho et al. | Ruthenium nanoparticles supported on hydroxyapatite as an efficient and recyclable catalyst for cis-dihydroxylation and oxidative cleavage of alkenes | |
Goto et al. | Synthesis, structural characterization, and catalytic performance of dititanium-substituted γ-Keggin silicotungstate | |
Zhang et al. | Anion-induced 3d–4f luminescent coordination clusters: structural characteristics and chemical fixation of CO 2 under mild conditions | |
Luz et al. | Selective aerobic oxidation of activated alkanes with MOFs and their use for epoxidation of olefins with oxygen in a tandem reaction | |
JPWO2002072257A1 (en) | Catalyst for producing epoxy compound and method for producing epoxy compound using the same | |
Huang et al. | Solvent-induced assembly of sliver coordination polymers (CPs) as cooperative catalysts for synthesizing of cyclopentenone [b] pyrroles frameworks | |
Chen et al. | Highly efficient epoxidation of allylic alcohols with hydrogen peroxide catalyzed by peroxoniobate-based ionic liquids | |
Zheng et al. | Two copper-containing polyoxometalate-based metal–organic complexes as heterogeneous catalysts for the C–H bond oxidation of benzylic compounds and olefin epoxidation | |
Mirzaee et al. | Preparation and characterization of Fe3O4@ Boehmite core‐shell nanoparticles to support molybdenum or vanadium complexes for catalytic epoxidation of alkenes | |
Maiti et al. | Oxo-and oxoperoxo-molybdenum (VI) complexes with aryl hydroxamates: Synthesis, structure, and catalytic uses in highly efficient, selective, and ecologically benign peroxidic epoxidation of olefins | |
Griffith et al. | The crystal structures of [NMe 4] 2 [(PhPO 3){MoO (O 2) 2} 2-{MoO (O 2) 2 (H 2 O)}] and [NBu n 4] 2 [W 4 O 6 (O 2) 6 (OH 2)(H 2 O) 2] and their use as catalytic oxidants | |
Duarte et al. | Homogeneous catalytic oxidation of olefins with hydrogen peroxide in the presence of a manganese-substituted polyoxomolybdate | |
Toda et al. | A phosphonium ylide as a ligand for [3+ 2] coupling reactions of epoxides with heterocumulenes under mild conditions | |
Samanta et al. | A mononuclear copper (II) complex immobilized in mesoporous silica: an efficient heterogeneous catalyst for the aerobic oxidation of benzylic alcohols | |
Taghiyar et al. | New perspective to catalytic epoxidation of olefins by Keplerate containing Keggin polyoxometalates | |
WO2009155185A1 (en) | Ruthenium-containing polyoxotungstates, their preparation and use as catalysts in the oxidation of organic substrates | |
Ma et al. | Peroxotantalate‐Based Ionic Liquid Catalyzed Epoxidation of Allylic Alcohols with Hydrogen Peroxide | |
Vrdoljak et al. | Dioxotungsten (VI) complexes with isoniazid-related hydrazones as (pre) catalysts for olefin epoxidation: solvent and ligand substituent effects | |
Qiao et al. | Polyoxometalate-based solid and liquid salts for catalysis |