Mehendale et al., 2006 - Google Patents
Novel silica immobilized NCN-pincer palladium (II) and platinum (II) complexes: Application as Lewis acid catalystsMehendale et al., 2006
View PDF- Document ID
- 12473936337016280354
- Author
- Mehendale N
- Bezemer C
- van Walree C
- Gebbink R
- van Koten G
- Publication year
- Publication venue
- Journal of Molecular Catalysis A: Chemical
External Links
Snippet
2, 6-Bis [(dimethylamino) methyl] phenyl (NCN-pincer) palladium (II) and platinum (II) complexes tethered to a trialkoxysilane coupling agent through a carbamate linkage were immobilized on various types of silica using a grafting or a sol–gel process. The resulting …
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide 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O=[Si]=O 0 title abstract description 171
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- 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
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- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C-Si linkages
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- 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
- B01J31/2282—Unsaturated compounds used as ligands
- B01J31/2295—Cyclic compounds, e.g. cyclopentadienyls
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- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/1608—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes the ligands containing silicon
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- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
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- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/1616—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts
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- C07F17/00—Metallocenes
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- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating; Solid sorbent compositions obtained from processes involving impregnating or coating
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/002—Osmium compounds
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- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
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- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/281—Sorbents specially adapted for preparative, analytical or investigative chromatography
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- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/46—Ruthenium, rhodium, osmium or iridium
- B01J23/462—Ruthenium
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- 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
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Wang et al. | Divalent silicon-assisted activation of dihydrogen in a bis (N-heterocyclic silylene) xanthene nickel (0) complex for efficient catalytic hydrogenation of olefins | |
Park et al. | Development and mechanistic investigation of a highly efficient iridium (V) silyl complex for the reduction of tertiary amides to amines | |
Piers et al. | Mechanistic aspects of bond activation with perfluoroarylboranes | |
Kleij et al. | A “dendritic effect” in homogeneous catalysis with carbosilane-supported arylnickel (II) catalysts: observation of active-site proximity effects in atom-transfer radical addition | |
Hashimoto et al. | Synthesis of bis (N-heterocyclic carbene) complexes of iron (II) and their application in hydrosilylation and transfer hydrogenation | |
Borowski et al. | Versatile Reactivity of the Bis (dihydrogen) Complex RuH2 (H2) 2 (PCy3) 2 toward Functionalized Olefins: Olefin Coordination versus Hydrogen Transfer via the Stepwise Dehydrogenation of the Phosphine Ligand | |
Maddock et al. | Insertion of Ethyne into the Ru− Si Bonds of Coordinatively Unsaturated Ruthenium Silyl Complexes. X-ray Crystal Structures of Ru (CH CHSiMe2OEt) Cl (CO) 2 (PPh3) 2 and [Ru (CH CHSiMe2OH)(CN-p-tolyl)(CO)(PPh3) 2] ClO4 | |
Sandee et al. | Solid‐phase synthesis of homogeneous ruthenium catalysts on silica for the continuous asymmetric transfer hydrogenation reaction | |
Molander et al. | Sequential cyclization/silylation of enynes catalyzed by an organoyttrium complex | |
Gorczyński et al. | The cobalt (II) complex of a new tridentate Schiff-base ligand as a catalyst for hydrosilylation of olefins | |
Monge-Marcet et al. | Sol–gel immobilized Hoveyda–Grubbs complex through the NHC ligand: A recyclable metathesis catalyst | |
Bhattacharya et al. | Activation of dihydrogen and silanes by cationic iron bis (phosphinite) pincer complexes | |
Royo | Recent advances in catalytic hydrosilylation of carbonyl groups mediated by well-defined first-row late transition metals | |
Michalska et al. | Synthesis and catalytic activity of the transition metal complex catalysts supported on the branched functionalized polysiloxanes grafted on silica | |
Adams et al. | Catalytic Hydrosilylation of Diarylalkynes by Layer-Segregated Platinum− Ruthenium Cluster Complexes Pt3Ru6 (CO) 20 (μ3-RC2R)(μ3-H)(μ-H) | |
Jakoobi et al. | Developing a highly active catalytic system based on cobalt nanoparticles for terminal and internal alkene hydrosilylation | |
Liu et al. | Iron-Catalyzed Regiodivergent Hydrostannation of Alkynes: Intermediacy of Fe (IV)–H versus Fe (II)–Vinylidene | |
Chang et al. | (NHC) Ni (0)-catalyzed branched-selective alkene hydrosilylation with secondary and tertiary silanes | |
Chen et al. | Noncovalent anchoring of homogeneous catalysts to silica supports with well-defined binding sites | |
Goni et al. | A methods study of immobilization of PONOP pincer transition metal complexes on silica polyamine composites (SPC) | |
Hu et al. | MCM-41-supported mercapto platinum complex as a highly efficient catalyst for the hydrosilylation of olefins with triethoxysilane | |
Gauvin et al. | Well‐Defined Silica‐Supported Calcium Reagents: Control of Schlenk Equilibrium by Grafting | |
Matsubara et al. | Homoleptic Cobalt (II) Phenoxyimine Complexes for Hydrosilylation of Aldehydes and Ketones without Base Activation of Cobalt (II) | |
Anjali et al. | Iridium Tetra (4‐carboxyphenyl) Porphyrin, Calix [4] pyrrole and Tetraphenyl Porphyrin Complexes as Potential Hydrogenation Catalysts |