Nothing Special   »   [go: up one dir, main page]

Mac Leod et al., 2012 - Google Patents

Copper (II) complexes of arylhydrazones of β-diketones immobilized on Zn–Al layered double hydroxides as effective recyclable catalysts for peroxidative oxidation of …

Mac Leod et al., 2012

View PDF
Document ID
12269029505771741945
Author
Mac Leod T
Kopylovich M
da Silva M
Mahmudov K
Pombeiro A
Publication year
Publication venue
Applied Catalysis A: General

External Links

Snippet

New CuII complexes [Cu (H2O)(μ-L1) Na (H2O)] n· 2nH2O (4),[Cu (H2O)(μ-HL2) Na (H2O)] n· 2nH2O (5) and [Cu (H2O)(μ-L3) Na (H2O)] n· 2nH2O (6), bearing the SO3− or COO−- functionalized arylhydrazones of β-diketones (AHBDs) 3-(2-hydroxy-3-sulfo-5 …
Continue reading at www.academia.edu (PDF) (other versions)

Classifications

    • 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
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • 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
    • 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
    • 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
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0213Complexes without C-metal linkages
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/48Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups
    • C07C29/50Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46Ruthenium, rhodium, osmium or iridium
    • B01J23/462Ruthenium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 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
    • B01J2231/70Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues

Similar Documents

Publication Publication Date Title
Mac Leod et al. Copper (II) complexes of arylhydrazones of β-diketones immobilized on Zn–Al layered double hydroxides as effective recyclable catalysts for peroxidative oxidation of alkanes
Rogge et al. Metal–organic and covalent organic frameworks as single-site catalysts
Ji et al. Tuning Lewis acidity of metal–organic frameworks via perfluorination of bridging ligands: spectroscopic, theoretical, and catalytic studies
Parida et al. Synthesis and characterization of a Fe (III)-Schiff base complex in a Zn-Al LDH host for cyclohexane oxidation
US10647733B2 (en) Metal-organic frameworks containing nitrogen-donor ligands for efficient catalytic organic transformations
Bhattacharjee et al. Synthesis and application of layered double hydroxide-hosted catalysts for stereoselective epoxidation using molecular oxygen or air
Guchhait et al. Oxo-and hydroxo-bridged diiron (III) porphyrin dimers: Inorganic and bio-inorganic perspectives and effects of intermacrocyclic interactions
Dhakshinamoorthy et al. Aerobic oxidation of cycloalkenes catalyzed by iron metal organic framework containing N-hydroxyphthalimide
Bhattacharjee et al. Comparison of the epoxidation of cyclohexene, dicyclopentadiene and 1, 5-cyclooctadiene over LDH hosted Fe and Mn sulfonato-salen complexes
Jin et al. Encapsulation of transition metal tetrahydro-Schiff base complexes in zeolite Y and their catalytic properties for the oxidation of cycloalkanes
Kirillov et al. Mild oxidative functionalization of alkanes and alcohols catalyzed by new mono-and dicopper (II) aminopolyalcoholates
Dhakshinamoorthy et al. Atmospheric‐Pressure, Liquid‐Phase, Selective Aerobic Oxidation of Alkanes Catalysed by Metal–Organic Frameworks
Liu et al. Synthesis, Structural Characterization, and Catalytic Performance of a Vanadium‐Based Metal–Organic Framework (COMOC‐3)
Liu et al. Bimetallic–Organic Framework as a Zero‐Leaching Catalyst in the Aerobic Oxidation of Cyclohexene
Angelescu et al. Epoxidation of cyclohexene with O2 and isobutyraldehyde catalysed by cobalt modified hydrotalcites
Kuźniarska-Biernacka et al. Manganese complexes with triazenido ligands encapsulated in NaY zeolite as heterogeneous catalysts
Moghadam et al. Molybdenum Schiff base-polyoxometalate hybrid compound: A heterogeneous catalyst for alkene epoxidation with tert-BuOOH
Tran et al. Deoxydehydration of polyols catalyzed by a molybdenum dioxo-complex supported by a dianionic ONO pincer ligand
Zamanifar et al. Synthesis, crystal structure and catalytic activity of a new Mo Schiff base complex with Mo histidine immobilized on Al-MCM-41 for oxidation of sulfides
Rostamnia et al. Pd (PrSO3) 2@ SBA-15 and Pd-NPs (PrSO3)@ SBA-15 hybrid materials: A highly active, reusable, and selective interface catalyst for C–X activations in air and water
Dasgupta et al. Ligand‐Flexibility Controlled and Solvent‐Induced Nuclearity Conversion in CuII‐Based Catecholase Models: A Deep Insight Through Combined Experimental and Theoretical Investigations
Dapurkar et al. Solvent-free allylic oxidation of cycloolefins over mesoporous CrMCM-41 molecular sieve catalyst at 1 atm dioxygen
Jin et al. Room temperature aqueous synthesis of Ce (IV)-MOFs with UiO-66 architecture and their photocatalytic decarboxylative oxygenation of arylacetic acids
Ionescu et al. Epoxidation of cyclohexene with H 2 O 2 and acetonitrile catalyzed by Mg–Al hydrotalcite and cobalt modified hydrotalcites
Mirkhani et al. Host (nanocavity of zeolite-Y)–guest (manganese (III) salophen complex) nanocomposite materials: an efficient catalyst for biomimetic alkene epoxidation and alkane hydroxylation with sodium periodate