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Quantitative 1,10-Phenanthroline Catalyst-Poisoning Kinetic Studies of Rh(0) Nanoparticle and Rh4Cluster Benzene Hydrogenation Catalysts: Estimates of the PoisonKassociationBinding Constants, of the Equivalents of Poison Bound and of the Number of Catalytically Active Sites for Each Catalyst
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0021-9517(86)90173-9openalex-snapshot
Dynamic response and poisoning studies of a liquid-solid catalytic reaction: Effects of metal content on adsorption and surface reaction rates
inferredcites →https://doi.org/10.1016/0021-9517(88)90328-4openalex-snapshot
Poisoning of thiophene hydrodesulfurization by nitrogen compounds
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Clusters and colloids: bridges between molecular and condensed material
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Binding of NAD+ to pertussis toxin
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Giant palladium clusters as catalysts of oxidative reactions of olefins and alcohols
inferredcites →https://doi.org/10.1016/j.cattod.2005.11.076openalex-snapshot
Combining operando techniques in one spectroscopic-reaction cell: New opportunities for elucidating the active site and related reaction mechanism in catalysis
inferredcites →https://doi.org/10.1016/j.molcata.2004.07.021openalex-snapshot
Phenanthroline-stabilized palladium nanoparticles in polyethylene glycol—an active and recyclable catalyst system for the selective hydrogenation of olefins using molecular hydrogen
inferredcites →https://doi.org/10.1016/j.molcata.2011.11.011openalex-snapshot
A review of the kinetics and mechanisms of formation of supported-nanoparticle heterogeneous catalysts
inferredcites →https://doi.org/10.1016/s0040-4039(00)90758-5openalex-snapshot
Homogeneous hydrogenation in the presence of sulphur compounds
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Effects of Surface Modifiers in the Liquid-Phase Hydrogenation of Olefins over Silica-Supported Pt, Pd and Rh Catalysts II. Thiophene and CS2
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Catalyst deactivation: How we cannot yet subvert nature
inferredcites →https://doi.org/10.1016/s0360-0564(08)60106-6openalex-snapshot
The Poisoning of Metallic Catalysts
inferredcites →https://doi.org/10.1016/s0360-0564(08)60454-xopenalex-snapshot
Sulfur Poisoning of Metals
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Mechanisms of catalyst deactivation
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A review of the problem of distinguishing true homogeneous catalysis from soluble or other metal-particle heterogeneous catalysis under reducing conditions
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(Pentamethylcyclopentadienyl)rhodium and -iridium complexes: approaches to new types of homogeneous catalysts
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Is There a Minimal Chemical Mechanism Underlying Classical Avrami-Erofe’ev Treatments of Phase-Transformation Kinetic Data?
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Hydrogenation of organic compounds using homogeneous catalysts
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Tuning the Chemoselectivity of Rh Nanoparticle Catalysts by Site-Selective Poisoning with Phosphine Ligands: The Hydrogenation of Functionalized Aromatic Compounds
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NaBr Poisoning of Au/TiO2 Catalysts: Effects on Kinetics, Poisoning Mechanism, and Estimation of the Number of Catalytic Active Sites
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Nanoclusters in Catalysis: A Comparison of CS2 Catalyst Poisoning of Polyoxoanion- and Tetrabutylammonium-Stabilized 40 ± 6 Å Rh(0) Nanoclusters to 5 Rh/Al2O3, Including an Analysis of the Literature Related to the CS2 to Metal Stoichiometry Issue
inferredcites →https://doi.org/10.1021/ie00020a012openalex-snapshot
Deactivation of methanol synthesis catalysts
inferredcites →https://doi.org/10.1021/ie040243qopenalex-snapshot
Hydrogenation of Polystyrene in CO2-Expanded Solvents: Catalyst Poisoning
inferredcites →https://doi.org/10.1021/j100529a011openalex-snapshot
Poisoning titration technique for determining the number of active centers in a supported platinum catalyst
inferredcites →https://doi.org/10.1021/ja00097a047openalex-snapshot
Novel Polyoxoanion- and Bu4N+-Stabilized, Isolable, and Redissolvable, 20-30-.ANG. Ir300-900 Nanoclusters: The Kinetically Controlled Synthesis, Characterization, and Mechanism of Formation of Organic Solvent-Soluble, Reproducible Size, and Reproducible Catalytic Activity Metal Nanoclusters
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THE CONSTITUTION AND FUNDAMENTAL PROPERTIES OF SOLIDS AND LIQUIDS. PART I. SOLIDS.
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Is It Homogeneous or Heterogeneous Catalysis Derived from [RhCp*Cl2]2?In OperandoXAFS, Kinetic, and Crucial Kinetic Poisoning Evidence for Subnanometer Rh4Cluster-Based Benzene Hydrogenation Catalysis
inferredcites →https://doi.org/10.1021/ja211658topenalex-snapshot
Iron Nanoparticles Catalyzing the Asymmetric Transfer Hydrogenation of Ketones
inferredcites →https://doi.org/10.1021/la101390eopenalex-snapshot
In Situ Formed “Weakly Ligated/Labile Ligand” Iridium(0) Nanoparticles and Aggregates as Catalysts for the Complete Hydrogenation of Neat Benzene at Room Temperature and Mild Pressures
inferredcites →https://doi.org/10.1021/la2049162openalex-snapshot
In Situ Formed Catalytically Active Ruthenium Nanocatalyst in Room Temperature Dehydrogenation/Dehydrocoupling of Ammonia-Borane from Ru(cod)(cot) Precatalyst
inferredcites →https://doi.org/10.1039/c39770000427openalex-snapshot
Stereoselective homogeneous hydrogenation of arenes to cyclohexanes catalysed by [Rh(η 5 -C 5 Me 5 )Cl 2 ] 2
inferredcites →https://doi.org/10.1063/1.1679027openalex-snapshot
Adsorbate interactions on a Pt(110) surface. I. Sulfur and carbon monoxide
inferredcites →https://doi.org/10.1080/00986440500191669openalex-snapshot
MODELING OF COMPETITIVE ADSORPTION OF NITROGEN SPECIES IN HYDRODESULFURIZATION
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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