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Tobias Adrian Engesser

Chemiker

Name	Tobias Adrian Engesser
Place	Karlsruhe (Geburtsort) Deutschland
Gender	männlich
Academic degree	Dr.
Profession	Chemiker (characteristic profession)
Variant	Tobias A. Engesser Tobias Engesser
Further information	Diss. 2016, Universität Freiburg, Fakultät für Chemie und Pharmazie
Record type	Person
GND-Identifier	1084023067
Record ID	1084023067
Involved in show all Chemokatalytische Umwandlung von Distickstoff zu Ammoniak vermittelt durch einen Wolframkomplex Chemocatalytic Conversion of Dinitrogen to Ammonia Mediated by a Tungsten Complex Nutzung des Perfluornaphthalin‐Radikalkations als selektiver Deelektronierer zur Erzeugung einer Vielzahl stark oxidierender reaktiver Kationen Utilizing the Perfluoronaphthalene Radical Cation as a Selective Deelectronator to Access a Variety of Strongly Oxidizing Reactive Cations From the Iron Pentacarbonyl Cation to Heteroleptic η 6 ‐arene Carbonyls and bis‐η 6 ‐arene Cations Dinucleating N ‐donor Ligands with 1,2‐Diethynylbenzene Backbone for the Copper‐Mediated Monooxygenation of Phenols Front Cover: Dinucleating N ‐donor Ligands with 1,2‐Diethynylbenzene Backbone for the Copper‐Mediated Monooxygenation of Phenols (Z. Anorg. Allg. Chem. 4/2024) From the iron pentacarbonyl cation to heteroleptic [my]6‐arene carbonyls and bis‐[my]6‐arene cations Nutzung des Perfluornaphthalin‐Radikalkations als selektiver Deelektronierer zur Erzeugung einer Vielzahl stark oxidierender reaktiver Kationen Utilizing the perfluoronaphthalene radical cation as a selective deelectronator to access a variety of strongly oxidizing reactive cations Oligodentate Aminotriazole Ligands for CuAAC and Copper‐Mediated Monooxygenation of Phenols: Influence of Denticity, Chain Length and N ‐Alkylation on Catalytic Activity Molybdenum Tricarbonyl Complexes Supported by Linear PNP Ligands: Influence of P ‐ and N ‐Substituents on Relative Stability, Stereoisomerism and on the Activation of Small Molecules Molybdenum Tricarbonyl Complexes Supported by Linear PNP Ligands: Influence of P ‐ and N ‐Substituents on Relative Stability, Stereoisomerism and on the Activation of Small Molecules Targeted Synthesis of an Highly Stable Aluminium Phosphonate Metal–Organic Framework Showing Reversible HCl Adsorption Targeted Synthesis of an Highly Stable Aluminium Phosphonate Metal–Organic Framework Showing Reversible HCl Adsorption N 2 Reduction versus H 2 Evolution in a Molybdenum‐ or Tungsten‐Based Small‐Molecule Model System of Nitrogenase N2 Reduction versus H2 Evolution in a Molybdenum- or Tungsten-Based Small-Molecule Model System of Nitrogenase Room‐Temperature Solid‐State Transformation of Na 4 SnS 4 ⋅ 14H 2 O into Na 4 Sn 2 S 6 ⋅ 5H 2 O: An Unusual Epitaxial Reaction Including Bond Formation, Mass Transport, and Ionic Conductivity Dinuclear Copper (I) Complexes Supported by Bis‐Tridentate N ‐Donor‐Ligands: Turning‐On Tyrosinase Activity Kupfer‐katalysierte Monooxygenierung von Phenolen: Evidenz für einen mononuklearen Reaktionsmechanismus Copper‐Catalyzed Monooxygenation of Phenols: Evidence for a Mononuclear Reaction Mechanism Copper-Catalyzed Monooxygenation of Phenols: Evidence for a Mononuclear Reaction Mechanism Copper‐catalyzed monooxygenation of phenols: evidence for a mononuclear reaction mechanism Dinuclear Copper(I) Complexes Supported by Bis‐Tridentate N‐Donor‐Ligands: Turning‐On Tyrosinase Activity Kupfer‐katalysierte Monooxygenierung von Phenolen : Evidenz für einen mononuklearen Reaktionsmechanismus Kupfer‐katalysierte Monooxygenierung von Phenolen: Evidenz für einen mononuklearen Reaktionsmechanismus Bonding and Activation of N 2 in Molybdenum(0) Complexes Supported by Tripod Ligands with Phospholane End Groups Metal‐Dependent and Selective Crystallization of CAU‐10 and MIL‐53 Frameworks through Linker Nitration Rhodium(III) and Ruthenium(II) Complexes with a Pentadentate Tetrapodal Phosphine Ligand Metal‐Dependent and Selective Crystallization of CAU‐10 and MIL‐53 Frameworks through Linker Nitration Oligodentate Phosphine Ligands with Phospholane End Groups: New Synthetic Access and Application to Molybdenum‐Based Synthetic Nitrogen Fixation A Chatt‐Type Catalyst with One Coordination Site for Dinitrogen Reduction to Ammonia A Chatt‐Type Catalyst with One Coordination Site for Dinitrogen Reduction to Ammonia Front Cover: A Chatt‐Type Catalyst with One Coordination Site for Dinitrogen Reduction to Ammonia (Chem. Eur. J. 65/2020) As–P vs. P–P Insertion in AsP 3: Kinetic Control of the Formation of (AsP 3 NO) + Employing Linear Tridentate Ligands with Pyrazole End Groups in Catalytic Tyrosinase Model Chemistry: Does Hemilability Matter? Homoleptic Trichloroacetonitrile Complexes Tyrosinase Model Systems Supported by Pyrazolylmethylpyridine Ligands: Electronic and Steric Factors Influencing the Catalytic Activity and Impact of Complex Equilibria in Solution Click. Coordinate. Catalyze. Using CuAAC Click Ligands in Small‐Molecule Model Chemistry of Tyrosinase Homoleptic Gold Acetonitrile Complexes with Medium to Very Weakly Coordinating Counterions: Effect on Aurophilicity? Reactive P-Block cations stabilized by weakly coordinating anions The synthesis of reactive gold(I) and phosphorus cations with nitrosyl salts of weakly coordinating anions (TeX 3) + Cations Stabilized by the Weakly Coordinating (Al (OR F) 4) − Anion: FIR Spectra, Raman Spectra, and Evaluation of an Abnormal Halogen Dependence of the 125 Te NMR Chemical Shifts † Endlich positiv: (P 9) + (Al{OC (CF 3) 3 } 4) −, das Salz eines homopolyatomaren Phosphorkations † Innentitelbild: Endlich positiv: (P 9) + (Al{OC (CF 3) 3 } 4) −, das Salz eines homopolyatomaren Phosphorkations (Angew. Chem. 26/2012) Inside Cover: (P 9) + (Al (OR F) 4) −, the Salt of a Homopolyatomic Phosphorus Cation (Angew. Chem. Int. Ed. 26/2012) Zwischen Komplex und Cluster: Ein 14‐eckiger Käfig in (Ag 2 Se 12) 2+ †

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Katalog der Deutschen Nationalbibliothek

Tobias Adrian Engesser

Chemokatalytische Umwandlung von Distickstoff zu Ammoniak vermittelt durch einen Wolframkomplex

Chemocatalytic Conversion of Dinitrogen to Ammonia Mediated by a Tungsten Complex

Nutzung des Perfluornaphthalin‐Radikalkations als selektiver Deelektronierer zur Erzeugung einer Vielzahl stark oxidierender reaktiver Kationen

Utilizing the Perfluoronaphthalene Radical Cation as a Selective Deelectronator to Access a Variety of Strongly Oxidizing Reactive Cations

From the Iron Pentacarbonyl Cation to Heteroleptic η 6 ‐arene Carbonyls and bis‐η 6 ‐arene Cations

Dinucleating N ‐donor Ligands with 1,2‐Diethynylbenzene Backbone for the Copper‐Mediated Monooxygenation of Phenols

Front Cover: Dinucleating N ‐donor Ligands with 1,2‐Diethynylbenzene Backbone for the Copper‐Mediated Monooxygenation of Phenols (Z. Anorg. Allg. Chem. 4/2024)

From the iron pentacarbonyl cation to heteroleptic [my]6‐arene carbonyls and bis‐[my]6‐arene cations

Nutzung des Perfluornaphthalin‐Radikalkations als selektiver Deelektronierer zur Erzeugung einer Vielzahl stark oxidierender reaktiver Kationen

Utilizing the perfluoronaphthalene radical cation as a selective deelectronator to access a variety of strongly oxidizing reactive cations

Oligodentate Aminotriazole Ligands for CuAAC and Copper‐Mediated Monooxygenation of Phenols: Influence of Denticity, Chain Length and N ‐Alkylation on Catalytic Activity

Molybdenum Tricarbonyl Complexes Supported by Linear PNP Ligands: Influence of P ‐ and N ‐Substituents on Relative Stability, Stereoisomerism and on the Activation of Small Molecules

Molybdenum Tricarbonyl Complexes Supported by Linear PNP Ligands: Influence of P ‐ and N ‐Substituents on Relative Stability, Stereoisomerism and on the Activation of Small Molecules

Targeted Synthesis of an Highly Stable Aluminium Phosphonate Metal–Organic Framework Showing Reversible HCl Adsorption

Targeted Synthesis of an Highly Stable Aluminium Phosphonate Metal–Organic Framework Showing Reversible HCl Adsorption

N 2 Reduction versus H 2 Evolution in a Molybdenum‐ or Tungsten‐Based Small‐Molecule Model System of Nitrogenase

N2 Reduction versus H2 Evolution in a Molybdenum- or Tungsten-Based Small-Molecule Model System of Nitrogenase

Room‐Temperature Solid‐State Transformation of Na 4 SnS 4 ⋅ 14H 2 O into Na 4 Sn 2 S 6 ⋅ 5H 2 O: An Unusual Epitaxial Reaction Including Bond Formation, Mass Transport, and Ionic Conductivity

Dinuclear Copper (I) Complexes Supported by Bis‐Tridentate N ‐Donor‐Ligands: Turning‐On Tyrosinase Activity

Kupfer‐katalysierte Monooxygenierung von Phenolen: Evidenz für einen mononuklearen Reaktionsmechanismus

Copper‐Catalyzed Monooxygenation of Phenols: Evidence for a Mononuclear Reaction Mechanism

Copper-Catalyzed Monooxygenation of Phenols: Evidence for a Mononuclear Reaction Mechanism

Copper‐catalyzed monooxygenation of phenols: evidence for a mononuclear reaction mechanism

Dinuclear Copper(I) Complexes Supported by Bis‐Tridentate N‐Donor‐Ligands: Turning‐On Tyrosinase Activity

Kupfer‐katalysierte Monooxygenierung von Phenolen : Evidenz für einen mononuklearen Reaktionsmechanismus

Kupfer‐katalysierte Monooxygenierung von Phenolen: Evidenz für einen mononuklearen Reaktionsmechanismus

Bonding and Activation of N 2 in Molybdenum(0) Complexes Supported by Tripod Ligands with Phospholane End Groups

Metal‐Dependent and Selective Crystallization of CAU‐10 and MIL‐53 Frameworks through Linker Nitration

Rhodium(III) and Ruthenium(II) Complexes with a Pentadentate Tetrapodal Phosphine Ligand

Metal‐Dependent and Selective Crystallization of CAU‐10 and MIL‐53 Frameworks through Linker Nitration

Oligodentate Phosphine Ligands with Phospholane End Groups: New Synthetic Access and Application to Molybdenum‐Based Synthetic Nitrogen Fixation

A Chatt‐Type Catalyst with One Coordination Site for Dinitrogen Reduction to Ammonia

A Chatt‐Type Catalyst with One Coordination Site for Dinitrogen Reduction to Ammonia

Front Cover: A Chatt‐Type Catalyst with One Coordination Site for Dinitrogen Reduction to Ammonia (Chem. Eur. J. 65/2020)

As–P vs. P–P Insertion in AsP 3: Kinetic Control of the Formation of (AsP 3 NO) +

Employing Linear Tridentate Ligands with Pyrazole End Groups in Catalytic Tyrosinase Model Chemistry: Does Hemilability Matter?

Homoleptic Trichloroacetonitrile Complexes

Tyrosinase Model Systems Supported by Pyrazolylmethylpyridine Ligands: Electronic and Steric Factors Influencing the Catalytic Activity and Impact of Complex Equilibria in Solution

Click. Coordinate. Catalyze. Using CuAAC Click Ligands in Small‐Molecule Model Chemistry of Tyrosinase

Homoleptic Gold Acetonitrile Complexes with Medium to Very Weakly Coordinating Counterions: Effect on Aurophilicity?

Reactive P-Block cations stabilized by weakly coordinating anions

The synthesis of reactive gold(I) and phosphorus cations with nitrosyl salts of weakly coordinating anions

(TeX 3) + Cations Stabilized by the Weakly Coordinating (Al (OR F) 4) − Anion: FIR Spectra, Raman Spectra, and Evaluation of an Abnormal Halogen Dependence of the 125 Te NMR Chemical Shifts †

Endlich positiv: (P 9) + (Al{OC (CF 3) 3 } 4) −, das Salz eines homopolyatomaren Phosphorkations †

Innentitelbild: Endlich positiv: (P 9) + (Al{OC (CF 3) 3 } 4) −, das Salz eines homopolyatomaren Phosphorkations (Angew. Chem. 26/2012)

Inside Cover: (P 9) + (Al (OR F) 4) −, the Salt of a Homopolyatomic Phosphorus Cation (Angew. Chem. Int. Ed. 26/2012)

Zwischen Komplex und Cluster: Ein 14‐eckiger Käfig in (Ag 2 Se 12) 2+ †