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A Stabilized μ-η2:η2 Peroxodicopper(II) Complex with a Secondary Diamine Ligand and Its Tyrosinase-like Reactivity

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Reversible Dioxygen Binding and Phenol Oxygenation in a Tyrosinase Model System

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Is the Bis(-oxo)dicopper Core Capable of Hydroxylating an Arene?

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Reactivity of Copper(I) Complexes Towards Dioxygen

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Copper-Dioxygen and Copper-Oxo Species Relevant to Copper Oxygenases and Oxidases

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Biomimetic modeling of copper oxidase reactivity

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Multicopper Oxidases and Oxygenases

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A New Cu(II) Side-on Peroxo Model Clarifies the Assignment of the Oxyhemocyanin Raman Spectrum

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Experimental Studies of the Interconversion of μ-η2:η2-Peroxo- and Bis(μ-oxo)dicopper Complexes

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A new model for dioxygen binding in hemocyanin. Synthesis, characterization, and molecular structure of the .mu.-.eta.2:.eta.2 peroxo dinuclear copper(II) complexes, [Cu(HB(3,5-R2pz)3)]2(O2) (R = isopropyl and Ph)

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Dioxygen-copper reactivity. Models for hemocyanin: Reversible O2 and CO binding to structurally characterized dicopper(I) complexes containing hydrocarbon-linked bis[2-(2-pyridyl)ethyl]amine units

inferredcites →https://doi.org/10.1021/ja002527hopenalex-snapshot

Differential Reactivity between Interconvertible Side-On Peroxo and Bis-μ-oxodicopper Isomers Using Peralkylated Diamine Ligands

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Contrasting Copper−Dioxygen Chemistry Arising from Alike Tridentate Alkyltriamine Copper(I) Complexes

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Oxygenation of Phenols to Catechols by A (μ-η2:η2-Peroxo)dicopper(II) Complex: Mechanistic Insight into the Phenolase Activity of Tyrosinase

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Fine-Tuning of Copper(I)-Dioxygen Reactivity by 2-(2-Pyridyl)ethylamine Bidentate Ligands

inferredcites →https://doi.org/10.1021/ja972946nopenalex-snapshot

Irreversible Reduction of Dioxygen by Simple Peralkylated Diamine−Copper(I) Complexes: Characterization and Thermal Stability of a [Cu2(μ-O)2]2+ Core

inferredcites →https://doi.org/10.1021/ja980687bopenalex-snapshot

Investigation of the Reactive Oxygen Intermediate in an Arene Hydroxylation Reaction Performed by Xylyl-Bridged Binuclear Copper Complexes

inferredcites →https://doi.org/10.1021/ja981283mopenalex-snapshot

Highly Regioselective Oxidative Polymerization of 4-Phenoxyphenol to Poly(1,4-phenylene oxide) Catalyzed by Tyrosinase Model Complexes

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Peroxo-, Oxo-, and Hydroxo-Bridged Dicopper Complexes: Observation of Exogenous Hydrocarbon Substrate Oxidation

inferredcites →https://doi.org/10.1021/ja983635vopenalex-snapshot

Exogenous Substrate Reactivity with a [Cu(III)2O2]2+ Core: Structural Implications

inferredcites →https://doi.org/10.1021/ja9918425openalex-snapshot

Spectroscopic and Electronic Structural Studies of the Cu(III)2Bis-μ-oxo Core and Its Relation to the Side-On Peroxo-Bridged Dimer

inferredcites →https://doi.org/10.1021/ja992017ropenalex-snapshot

Re-engineering Enzyme-Model Active Sites: Reversible Binding of Dioxygen at Ambient Conditions by a Bioinspired Copper Complex

inferredcites →https://doi.org/10.1021/ja992295qopenalex-snapshot

Crystal Structure and Reversible O2-Binding of a Room Temperature Stable μ-η2:η2-Peroxodicopper(II) Complex of a Sterically Hindered Hexapyridine Dinucleating Ligand

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Novel tert-Butyl Migration in Copper-Mediated Phenol Ortho-Oxygenation Implicates a Mechanism Involving Conversion of a 6-Hydroperoxy-2,4-cyclohexadienone Directly to an o-Quinone

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A Trinuclear Intermediate in the Copper-Mediated Reduction of O 2 : Four Electrons from Three Coppers

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Orbital Analysis Of Oxo And Peroxo Dicopper Complexes Via Quantum Chemical Workflows In Mosgrid

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Structure, Spectroscopy, and Function of Tyrosinase; Comparison with Hemocyanin and Catechol Oxidase

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Organic Synthetic Methods Using Copper Oxygen Chemistry

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Developing Molecular Copper Complexes for Water Oxidation

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Structure, Spectroscopy, and Function of Tyrosinase; Comparison with Hemocyanin and Catechol Oxidase

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O 2 Reactivity at Model Copper Systems: Mimicking Tyrosinase Activity

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Katalytische Phenolhydroxylierung mit Sauerstoff: Substratvielfalt jenseits der Proteinmatrix von Tyrosinase

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Catalytic Phenol Hydroxylation with Dioxygen: Extension of the Tyrosinase Mechanism beyond the Protein Matrix

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Selective Ortho‐Hydroxylation–Defluorination of 2‐Fluorophenolates with a Bis(μ‐oxo)dicopper(III) Species

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Imidazolate‐Stabilized Cu(III): Dioxygen to Oxides at Type 3 Copper Sites

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Oxidative coupling of 2,6‐dimethylphenol catalyzed by copper(II) complexes in aqueous solution

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Quantitative Evaluation of d–π Interaction in Copper( i) Complexes and Control of Copper( i) –Dioxygen Reactivity

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Theoretical Study of the Oxidation of Phenolates by the [Cu 2 O 2 ( N , N ′‐di‐ tert ‐butylethylenediamine) 2 ] 2+ Complex

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Bioinspired Copper(I) Complexes that Exhibit Monooxygenase and Catechol Dioxygenase Activity

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Structure, Bonding, and Tyrosinase‐Like Reactivity of Copper Complexes Coordinated by Mononucleating Tridentate N−O−N Type Ligands

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Tuning of Copper( I )–Dioxygen Reactivity by Bis(guanidine) Ligands

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BOX Ligands in Biomimetic Copper‐Mediated Dioxygen Activation: A Hemocyanin Model

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Formation of Hybrid Guanidine‐Stabilized Bis(μ‐oxo)dicopper Cores in Solution: Electronic and Steric Perturbations

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Reactivity of Copper Complexes with Bis(piperidinyl)methane and Bis(quinolinyl)methane Ligands

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Anorganische Chemie 2002

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Organische Chemie 2002

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Aerial Oxidation of Alcohols by an Amide and Imidazole Functionalized Bioinspired Cu‐Complex and Its Switching with N‐Oxides

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Dioxygen-Binding in Metalloproteins and Corresponding Models

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O–O Bond Activation in Cu- and Fe-Based Coordination Complexes: Breaking It Makes the Difference

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Kinetic characterization of a bioinspired, heterogeneously active macromolecular catalyst for phenol oxidation and coupling reactions

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Hydroxylation of p-substituted phenols by tyrosinase: Further insight into the mechanism of tyrosinase activity

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The complexes of multiimidazole with copper(I) display tyrosinase activity

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Hydroxylation of a methyl group: synthesis of [Cu2(btmmO)2I]+ and of [Cu2(btmmO)2]2+ containing the novel ligand {bis(trimethylmethoxy)guanidino}propane (btmmO) by copper-assisted oxygen activation

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Spectrophotometric determination of formation constants for the Cu–ethylenediamine–halogen (chloride and bromide) system and their catalytic effect on the oxidative coupling of 2,6-di-tert-butyl-phenol

inferred← citeshttps://doi.org/10.1016/j.ica.2013.02.021openalex-snapshot

Spectrophotometric determination of the formation constants of the cupric halogen complexes with 1,3-propanediamine and 1,4-butanediamine in methanol solution and their activity on the oxidative coupling of the 2,6-di-tert-butylphenol

inferred← citeshttps://doi.org/10.1016/j.ica.2013.12.009openalex-snapshot

A comparative study of the speciation in methanol solution and activity in the oxidative coupling of 2,6-di-tert-butylphenol presented by the complexes: Copper(II)-N,N′-di-tert-butylethylenediamine-halogen and some copper(II)-diamine-halogen complexes

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Copper(II)-assisted hydrolysis of cyclic ureas: Transformation of 1-(pyridin-2-yl)-2,3,7,8-tetrahydro-1H-imidazo[2,1-b][1,3,5]triazepin-5(6H)-ones into N1-[1-(pyridin-2-yl)imidazolidin-2-ylidene]-ethane-1,2-diamine ligands

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Cu-ZSM-5: A biomimetic inorganic model for methane oxidation

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A room temperature catalyst for toluene aliphatic C–H bond oxidation: Tripodal tridentate copper complex immobilized in mesoporous silica

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Mechanism studies of oxidation and hydrolysis of Cu(I)–NHC and Ag–NHC in solution under air

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Adenine supported hydroxyl-bridged dicopper core as a catalytically competent unit for phenol oxidation

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15 Copper

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Alkane hydroperoxidation with peroxides catalysed by copper complexes

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Spectroscopic characterization of the oxo-transfer reaction from a bis(μ-oxo)dicopper( iii ) complex to triphenylphosphine

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