Ren et al., 2016 - Google Patents

A heterometal (Pd–Pb) organic framework: synthesis, structure and heterogeneous catalytic application

Ren et al., 2016

Document ID
17402018036971350014
Author
Ren Y
Jiang O
Li J
Zeng H
Publication year
Publication venue
Applied Organometallic Chemistry

External Links

Snippet

A heterometallic organic framework {Pb [Pd (bpydc) Cl2] DMF} n (1)(H2bpydc= 2, 2′‐ bipyridine‐5, 5′‐dicarboxylic acid) was synthesized via a one‐pot solvothermal method and characterized using thermogravimetric analysis, X‐ray photoelectron spectroscopy as …
Continue reading at onlinelibrary.wiley.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic System
    • C07F5/02Boron 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
    • B01J31/16Catalysts 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
    • 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

Similar Documents

Publication Publication Date Title
Shyshkanov et al. In situ formation of frustrated lewis pairs in a water‐tolerant metal‐organic framework for the transformation of CO2
Li et al. A Reusable MOF‐Supported Single‐Site Zinc (II) Catalyst for Efficient Intramolecular Hydroamination of o‐Alkynylanilines
Tu et al. Rational design of catalytic centers in crystalline frameworks
Dhakshinamoorthy et al. Formation of C–C and C–heteroatom bonds by C–H activation by metal organic frameworks as catalysts or supports
Zhou et al. Conjugated microporous polymer as heterogeneous ligand for highly selective oxidative Heck reaction
Chan et al. A Radical Process towards the Development of Transition‐Metal‐Free Aromatic Carbon Carbon Bond‐Forming Reactions
Shang et al. Graphene oxide supported N-heterocyclic carbene-palladium as a novel catalyst for the Suzuki–Miyaura reaction
Huang et al. A Rhenium‐Functionalized Metal–Organic Framework as a Single‐Site Catalyst for Photochemical Reduction of Carbon Dioxide
Dutta et al. Encapsulation of Silver Nanoparticles in an Amine‐Functionalized Porphyrin Metal–Organic Framework and Its Use as a Heterogeneous Catalyst for CO2 Fixation under Atmospheric Pressure
Mousavi et al. CO2 cycloaddition to epoxides by using M‐DABCO metal–Organic frameworks and the influence of the synthetic method on catalytic reactivity
Yuan et al. N‐Heterocyclic Carbene–Ytterbium Amide as a Recyclable Homogeneous Precatalyst for Hydrophosphination of Alkenes and Alkynes
Diyali et al. Metal–organic framework: An emergent catalyst in C–N cross-coupling reactions
García-García et al. Organic–inorganic supramolecular solid catalyst boosts organic reactions in water
Zhao et al. Shape-controllable formation of poly-imidazolium salts for stable palladium N-heterocyclic carbene polymers
Kempasiddhaiah et al. Magnetite tethered mesoionic carbene‐palladium (II): An efficient and reusable nanomagnetic catalyst for Suzuki‐Miyaura and Mizoroki‐Heck cross‐coupling reactions in aqueous medium
Dong et al. Crosslinked resin‐supported bifunctional organocatalyst for conversion of CO2 into cyclic carbonates
Sadhasivam et al. Incorporating Pd (OAc) 2 on Imine Functionalized Microporous Covalent Organic Frameworks: A Stable and Efficient Heterogeneous Catalyst for Suzuki‐Miyaura Coupling in Aqueous Medium
Nayan Sharma et al. Thioether–NHC‐Ligated PdII Complex for Crafting a Filtration‐Free Magnetically Retrievable Catalyst for Suzuki–Miyaura Coupling in Water
Ma et al. Dinuclear Pd (II)–NHC complex derived from proline and its application toward Mizoroki–Heck reaction performed in water
Zhang et al. Highly Regioselective Cobalt‐Catalyzed Hydroboration of Internal Alkynes
Gholinejad et al. Active palladium catalyst supported by bulky diimine ligand catalyzed Suzuki–Miyaura coupling reaction in water under phosphane‐free and low catalyst loading conditions
Tang et al. Amino‐Induced 2D Cu‐Based Metal–Organic Framework as an Efficient Heterogeneous Catalyst for Aerobic Oxidation of Olefins
Penafiel et al. (NHC) Palladium Complexes from Hydroxy‐Functionalized Imidazolium Salts as Catalyst for the Microwave‐Accelerated Fluorine‐Free Hiyama Reaction
Wen et al. A Triptycene‐Based Microporous Organic Polymer Bearing Tridentate Ligands and Its Application in Suzuki–Miyaura Cross‐Coupling Reaction
Xiong et al. One‐Pot Palladium‐Catalyzed Carbonylative Sonogashira Coupling using Carbon Dioxide as Carbonyl Source