[go: up one dir, main page]

Tarnowicz‐Ligus et al., 2019 - Google Patents

Incorporation of PdCl2P2 Complexes in Ni‐MOF for Catalyzing Heck Arylation of Functionalized Olefins

Tarnowicz‐Ligus et al., 2019

Document ID
12068535007596829998
Author
Tarnowicz‐Ligus S
Augustyniak A
Trzeciak A
Publication year
Publication venue
European Journal of Inorganic Chemistry

External Links

Snippet

Two palladium complexes of a PdCl2P2 type with P= tri (1‐piperidinyl) phosphine (Pd‐1) and triphenylphosphine (Pd‐2) were successfully immobilized on [Ni8 (OH) 4 (OH2) 2 (L) 6] n (Ni‐MOF) material [L= 4, 4′‐(benzene‐1, 4‐diyldiethyne‐2, 1‐diyl) bis (1‐H‐pyrazole)] to …
Continue reading at chemistry-europe.onlinelibrary.wiley.com (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
    • B01J31/22Organic complexes
    • B01J31/2282Unsaturated compounds used as ligands
    • B01J31/2295Cyclic compounds, e.g. cyclopentadienyls
    • 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
    • B01J31/181Cyclic ligands, including non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1825Ligands comprising condensed ring systems, e.g. acridine, carbazole
    • 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
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • 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
    • B01J31/02Catalysts 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
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/28Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
    • 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
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic 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
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds

Similar Documents

Publication Publication Date Title
Carson et al. Ruthenium complexation in an aluminium metal–organic framework and its application in alcohol oxidation catalysis
Heuzé et al. Copper‐Free Monomeric and Dendritic Palladium Catalysts for the Sonogashira Reaction: Substituent Effects, Synthetic Applications, and the Recovery and Re‐Use of the Catalysts
Corma et al. Cu and Au metal–organic frameworks bridge the gap between homogeneous and heterogeneous catalysts for alkene cyclopropanation reactions
Bloch et al. Capturing snapshots of post-synthetic metallation chemistry in metal–organic frameworks
Tarnowicz‐Ligus et al. Incorporation of PdCl2P2 Complexes in Ni‐MOF for Catalyzing Heck Arylation of Functionalized Olefins
Luz et al. Pd@ UiO‐66‐Type MOFs Prepared by Chemical Vapor Infiltration as Shape‐Selective Hydrogenation Catalysts
Garnovskii et al. Direct synthesis of coordination and organometallic compounds
Hurst et al. N-Heterocyclic carbene coated metal nanoparticles
Bézier et al. Applications of PC (sp3) P iridium complexes in transfer dehydrogenation of alkanes
Zhang et al. Chiral Bidentate Bis (N‐Heterocyclic Carbene)‐Based Palladium Complexes Bearing Carboxylate Ligands: Highly Effective Catalysts for the Enantioselective Conjugate Addition of Arylboronic Acids to Cyclic Enones
Morel et al. Synthesis and Characterization of Phosphine-Functionalized Metal–Organic Frameworks Based on MOF-5 and MIL-101 Topologies
Liori et al. A Sustainable, User‐Friendly Protocol for the Pd‐Free Sonogashira Coupling Reaction
WO2015149072A1 (en) Metal-organic frameworks containing nitrogen-donor ligands for efficient catalytic organic transformations
Zhu et al. Lanthanide metal-organic frameworks with six-coordinated ln (iii) ions and free functional organic sites for adsorptions and extensive catalytic activities
Shi et al. Development of a continuous‐flow system for asymmetric hydrogenation using self‐supported chiral catalysts
Perekalin et al. Synthesis of Ruthenium Half‐Sandwich Complexes by Naphthalene Replacement in [CpRu (C10H8)]+
CA2780010A1 (en) Metal colloids with accessible metal surfaces
Teci et al. N‐Heterocyclic Carbenes Functioning as Monoligating Clamps
Ojwach et al. (Pyridyl) benzoazole palladium (II) complexes as homogeneous catalysts in hydrogenation of alkenes and alkynes
Nagarjun et al. Copper (II)‐Doped ZIF‐8 as a Reusable and Size Selective Heterogeneous Catalyst for the Hydrogenation of Alkenes using Hydrazine Hydrate
Tubaro et al. Polynuclear Copper (I) Complexes with Chelating Bis‐and Tris‐N‐Heterocyclic Carbene Ligands: Catalytic Activity in Nitrene and Carbene Transfer Reactions
Kassie et al. Catalytic Activity of a Zr MOF Containing POCOP-Pd Pincer Complexes
Coulson et al. Carbon Nitride as a Ligand: Selective Hydrogenation of Terminal Alkenes Using [(η5‐C5Me5) IrCl (g‐C3N4‐κ2N, N’)] Cl
Hofmann et al. . eta. 2-(C, O) Ketene coordination at nickel (O). Synthesis, bonding, and molecular structure of (dtbpm) Ni [. eta. 2-(C, O)-Ph2C2O][dtbpm= bis (di-tert-butylphosphino) methane]
Sun et al. Synthesis, Structure, Reactivity, and Catalytic Activity of Cyclometalated (Phosphine)‐and (Phosphinite) ruthenium Complexes