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Martin K. Beyer (1969-)

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Name	Martin K. Beyer
Time	1969- (Date of birth and death)
Place	Ingolstadt (Geburtsort) Kiel (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Prof. Dr.
Profession	Physiker (characteristic profession)
Variant	M. K. Beyer Martin Beyer
Related	Christian-Albrechts-Universität zu Kiel. Institut für Physikalische Chemie
Further information	Diss. München 1999; Prof. für Physikalische Chemie an der Christian-Albrechts-Universität Kiel
Record type	Person
GND-Identifier	1016363753
Record ID	1016363753
Involved in show all X-ray absorption spectroscopy of FeH+ to aid its identification in astrochemical environments Proton Transfer Reactions from N 2 H + and ArH + to Small Molecules Thermally Activated vs. Photochemical Hydrogen Evolution Reactions–A Tale of Three Metals Frontispiece: Thermally Activated vs. Photochemical Hydrogen Evolution Reactions–A Tale of Three Metals Formation of Temporary Negative Ions and Their Subsequent Fragmentation upon Electron Attachment to CoQ 0 and CoQ 0 H 2 Formation of Temporary Negative Ions and Their Subsequent Fragmentation upon Electron Attachment to CoQ 0 and CoQ 0 H 2 Front Cover: Formation of Temporary Negative Ions and Their Subsequent Fragmentation upon Electron Attachment to CoQ 0 and CoQ 0 H 2 (ChemPhysChem 5/2022) Decomposition of halogenated molybdenum sulfide dianions [Mo3S7X6]2– (X = Cl, Br, I) Rearrangement and decomposition pathways of bare and hydrogenated molybdenum oxysulfides in the gas phase Photochemical Hydrogen Evolution at Metal Centers Probed with Hydrated Aluminium Cations, Al + (H 2 O) n , n =1–10 Photochemical Hydrogen Evolution at Metal Centers Probed with Hydrated Aluminium Cations, Al + (H 2 O) n , n =1–10 Auf zur Wasserstoffentwicklung: Das Infrarot‐Spektrum von hydratisiertem Aluminiumhydrid‐Hydroxid HAlOH + (H 2 O) n −1 , n= 9–14 Getting Ready for the Hydrogen Evolution Reaction: The Infrared Spectrum of Hydrated Aluminum Hydride–Hydroxide HAlOH + (H 2 O) n −1 , n= 9–14 Activation of a Copper Biscarbene Mechano‐Catalyst Using Single‐Molecule Force Spectroscopy Supported by Quantum Chemical Calculations Activation of a Copper Biscarbene Mechano‐Catalyst Using Single‐Molecule Force Spectroscopy Supported by Quantum Chemical Calculations Functionalization of Diamond‐Like Carbon Surfaces to Access High Rupture Forces in Single‐Molecule Force Spectroscopy of Covalent Bonds [Mo 3 S 13 ] 2− als Modellsystem für die katalytische Wasserstoffentwicklung durch MoS x : Untersuchung der Protonierungsstellen in der Gasphase durch Infrarot‐Mehrphotonendissoziationsspektroskopie Frontispiz: Auf zur Wasserstoffentwicklung: Das Infrarot‐Spektrum von hydratisiertem Aluminiumhydrid‐Hydroxid HAlOH + (H 2 O) n −1 , n= 9–14 [Mo 3 S 13 ] 2− as a Model System for Hydrogen Evolution Catalysis by MoS x : Probing Protonation Sites in the Gas Phase by Infrared Multiple Photon Dissociation Spectroscopy Frontispiece: Getting Ready for the Hydrogen Evolution Reaction: The Infrared Spectrum of Hydrated Aluminum Hydride–Hydroxide HAlOH + (H 2 O) n −1 , n= 9–14 [Mo 3 S 3] 2− als Modellsystem für die katalytische Wasserstoffentwicklung durch MoSx : : Untersuchung der Protonierungsstellen in der Gasphase durch Infrarot‐Mehrphotonendissoziationsspektroskopie [Mo3S13]2- as a model system for hydrogen evolution catalysis by MoSx: Probing protonation sites in the gas phase by infrared multiple photon dissociation spectroscopy Proton transfer reactivity of molybdenum oxysulfide dianions [Mo2O2S6]2- and [Mo2O2S5]2-: the role of Coulomb barriers Photochemical activation of carbon dioxide in Mg+(CO2)(H2O)0,1 UV/Vis Spectroscopy of Copper Formate Clusters: Insight into Metal‐Ligand Photochemistry Chemistry of NO x and HNO 3 Molecules with Gas‐Phase Hydrated O. − and OH − Ions Infrared Multiple Photon Dissociation Spectroscopy of Hydrated Cobalt Anions Doped with Carbon Dioxide CoCO 2 (H 2 O) n −, n =1–10, in the C−O Stretch Region Aktivierung von Kohlenstoffdioxid an Metallzentren: Entwicklung des Ladungstransfers von Mg . + auf CO 2 in (MgCO 2 (H 2 O) n). +, n= 0–8 Carbon Dioxide Activation at Metal Centers: Evolution of Charge Transfer from Mg . + to CO 2 in (MgCO 2 (H 2 O) n). +, n= 0–8 Structural Properties of Gas-Phase Molybdenum Oxide Clusters [Mo4O13]2−, [HMo4O13]−, and [CH3Mo4O13]− Studied by Collision-Induced Dissociation Release of Formic Acid from Copper Formate: Hydride, Proton‐Coupled Electron and Hydrogen Atom Transfer All Play their Role Infrared Spectroscopy of Size‐Selected Hydrated Carbon Dioxide Radical Anions CO 2. − (H 2 O) n (n =2–61) in the C−O Stretch Region Mechanical Activation Drastically Accelerates Amide Bond Hydrolysis, Matching Enzyme Activity Photodissociation of Sodium Iodide Clusters Doped with Small Hydrocarbons Gas-Phase Reactivity Studies of Small Molybdenum Cluster Ions with Dimethyl Disulfide Electrons Mediate the Gas‐Phase Oxidation of Formic Acid with Ozone Mechanochemical Cycloreversion of Cyclobutane Observed at the Single Molecule Level Lokalisierung eines mechanochemischen Bindungsbruchs durch Einbettung des Mechanophors in einen Makrocyclus † Durch Schwarzkörperstrahlung angetriebene chemische Reaktivität auf Metallclustern in der Gasphase † Pinpointing Mechanochemical Bond Rupture by Embedding the Mechanophore into a Macrocycle † Chemical Reactivity on Gas‐Phase Metal Clusters Driven by Blackbody Infrared Radiation † Mechanically induced silyl ester cleavage under acidic conditions investigated by AFM-based single-molecule force spectroscopy in the force-ramp mode Reduction of Acetonitrile by Hydrated Magnesium Cations Mg + (H 2 O) n (n ≈20–60) in the Gas Phase Reactions of Hydrated Singly Charged First‐Row Transition‐Metal Ions M + (H 2 O) n (M=V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) toward Nitric Oxide in the Gas Phase Gas‐Phase Reactions of Cationic Vanadium‐Phosphorus Oxide Clusters with C 2 H x (x= 4, 6): A DFT‐Based Analysis of Reactivity Patterns ChemInform Abstract: Reactions of Hydrated Singly Charged First‐Row Transition‐Metal Ions M + (H 2 O) n (M: V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) Toward Nitric Oxide in the Gas Phase. Carboxylierung von Methylacrylat durch das Kohlendioxid‐Radikalanion in Wasserclustern † Innentitelbild: Carboxylierung von Methylacrylat durch das Kohlendioxid‐Radikalanion in Wasserclustern (Angew. Chem. 35/2013) Carboxylation of Methyl Acrylate by Carbon Dioxide Radical Anions in Gas‐Phase Water Clusters † Inside Cover: Carboxylation of Methyl Acrylate by Carbon Dioxide Radical Anions in Gas‐Phase Water Clusters (Angew. Chem. Int. Ed. 35/2013) Über die Rolle von (CuO) + bei spinselektiven Wasserstoff‐ und Sauerstoff‐Übertragungen in der Aktivierung von Methan † Rücktitelbild: Über die Rolle von (CuO) + bei spinselektiven Wasserstoff‐ und Sauerstoff‐Übertragungen in der Aktivierung von Methan (Angew. Chem. 21/2011) Darstellung, Reaktivität gegenüber Kohlenwasserstoffen und elektronische Struktur von heteronuclearen Vanadium‐Phosphor‐Sauerstoff‐Clusterionen † Diatomic (CuO) + and Its Role in the Spin‐Selective Hydrogen‐ and Oxygen‐Atom Transfers in the Thermal Activation of Methane † Back Cover: Diatomic (CuO) + and Its Role in the Spin‐Selective Hydrogen‐ and Oxygen‐Atom Transfers in the Thermal Activation of Methane (Angew. Chem. Int. Ed. 21/2011) Generation, Reactivity Towards Hydrocarbons, and Electronic Structure of Heteronuclear Vanadium Phosphorous Oxygen Cluster Ions † Mechanically activated rupture of single covalent bonds: evidence of force induced bond hydrolysis. Selective Formic Acid Synthesis from Nanoscale Electrochemistry † Selective Formic Acid Synthesis from Nanoscale Electrochemistry † ChemInform Abstract: Thermal N—H Bond Activation on Anionic and Cationic Platinum Clusters: Non‐Predetermined Reaction Pathways Indicate Transitions to a Bulk Surface Reactivity.

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Katalog der Deutschen Nationalbibliothek

Martin K. Beyer (1969-)

X-ray absorption spectroscopy of FeH+ to aid its identification in astrochemical environments

Proton Transfer Reactions from N 2 H + and ArH + to Small Molecules

Thermally Activated vs. Photochemical Hydrogen Evolution Reactions–A Tale of Three Metals

Frontispiece: Thermally Activated vs. Photochemical Hydrogen Evolution Reactions–A Tale of Three Metals

Formation of Temporary Negative Ions and Their Subsequent Fragmentation upon Electron Attachment to CoQ 0 and CoQ 0 H 2

Formation of Temporary Negative Ions and Their Subsequent Fragmentation upon Electron Attachment to CoQ 0 and CoQ 0 H 2

Front Cover: Formation of Temporary Negative Ions and Their Subsequent Fragmentation upon Electron Attachment to CoQ 0 and CoQ 0 H 2 (ChemPhysChem 5/2022)

Decomposition of halogenated molybdenum sulfide dianions [Mo3S7X6]2– (X = Cl, Br, I)

Rearrangement and decomposition pathways of bare and hydrogenated molybdenum oxysulfides in the gas phase

Photochemical Hydrogen Evolution at Metal Centers Probed with Hydrated Aluminium Cations, Al + (H 2 O) n , n =1–10

Photochemical Hydrogen Evolution at Metal Centers Probed with Hydrated Aluminium Cations, Al + (H 2 O) n , n =1–10

Auf zur Wasserstoffentwicklung: Das Infrarot‐Spektrum von hydratisiertem Aluminiumhydrid‐Hydroxid HAlOH + (H 2 O) n −1 , n= 9–14

Getting Ready for the Hydrogen Evolution Reaction: The Infrared Spectrum of Hydrated Aluminum Hydride–Hydroxide HAlOH + (H 2 O) n −1 , n= 9–14

Activation of a Copper Biscarbene Mechano‐Catalyst Using Single‐Molecule Force Spectroscopy Supported by Quantum Chemical Calculations

Activation of a Copper Biscarbene Mechano‐Catalyst Using Single‐Molecule Force Spectroscopy Supported by Quantum Chemical Calculations

Functionalization of Diamond‐Like Carbon Surfaces to Access High Rupture Forces in Single‐Molecule Force Spectroscopy of Covalent Bonds

[Mo 3 S 13 ] 2− als Modellsystem für die katalytische Wasserstoffentwicklung durch MoS x : Untersuchung der Protonierungsstellen in der Gasphase durch Infrarot‐Mehrphotonendissoziationsspektroskopie

Frontispiz: Auf zur Wasserstoffentwicklung: Das Infrarot‐Spektrum von hydratisiertem Aluminiumhydrid‐Hydroxid HAlOH + (H 2 O) n −1 , n= 9–14

[Mo 3 S 13 ] 2− as a Model System for Hydrogen Evolution Catalysis by MoS x : Probing Protonation Sites in the Gas Phase by Infrared Multiple Photon Dissociation Spectroscopy

Frontispiece: Getting Ready for the Hydrogen Evolution Reaction: The Infrared Spectrum of Hydrated Aluminum Hydride–Hydroxide HAlOH + (H 2 O) n −1 , n= 9–14

[Mo 3 S 3] 2− als Modellsystem für die katalytische Wasserstoffentwicklung durch MoSx : : Untersuchung der Protonierungsstellen in der Gasphase durch Infrarot‐Mehrphotonendissoziationsspektroskopie

[Mo3S13]2- as a model system for hydrogen evolution catalysis by MoSx: Probing protonation sites in the gas phase by infrared multiple photon dissociation spectroscopy

Proton transfer reactivity of molybdenum oxysulfide dianions [Mo2O2S6]2- and [Mo2O2S5]2-: the role of Coulomb barriers

Photochemical activation of carbon dioxide in Mg+(CO2)(H2O)0,1

UV/Vis Spectroscopy of Copper Formate Clusters: Insight into Metal‐Ligand Photochemistry

Chemistry of NO x and HNO 3 Molecules with Gas‐Phase Hydrated O. − and OH − Ions

Infrared Multiple Photon Dissociation Spectroscopy of Hydrated Cobalt Anions Doped with Carbon Dioxide CoCO 2 (H 2 O) n −, n =1–10, in the C−O Stretch Region

Aktivierung von Kohlenstoffdioxid an Metallzentren: Entwicklung des Ladungstransfers von Mg . + auf CO 2 in (MgCO 2 (H 2 O) n). +, n= 0–8

Carbon Dioxide Activation at Metal Centers: Evolution of Charge Transfer from Mg . + to CO 2 in (MgCO 2 (H 2 O) n). +, n= 0–8

Structural Properties of Gas-Phase Molybdenum Oxide Clusters [Mo4O13]2−, [HMo4O13]−, and [CH3Mo4O13]− Studied by Collision-Induced Dissociation

Release of Formic Acid from Copper Formate: Hydride, Proton‐Coupled Electron and Hydrogen Atom Transfer All Play their Role

Infrared Spectroscopy of Size‐Selected Hydrated Carbon Dioxide Radical Anions CO 2. − (H 2 O) n (n =2–61) in the C−O Stretch Region

Mechanical Activation Drastically Accelerates Amide Bond Hydrolysis, Matching Enzyme Activity

Photodissociation of Sodium Iodide Clusters Doped with Small Hydrocarbons

Gas-Phase Reactivity Studies of Small Molybdenum Cluster Ions with Dimethyl Disulfide

Electrons Mediate the Gas‐Phase Oxidation of Formic Acid with Ozone

Mechanochemical Cycloreversion of Cyclobutane Observed at the Single Molecule Level

Lokalisierung eines mechanochemischen Bindungsbruchs durch Einbettung des Mechanophors in einen Makrocyclus †

Durch Schwarzkörperstrahlung angetriebene chemische Reaktivität auf Metallclustern in der Gasphase †

Pinpointing Mechanochemical Bond Rupture by Embedding the Mechanophore into a Macrocycle †

Chemical Reactivity on Gas‐Phase Metal Clusters Driven by Blackbody Infrared Radiation †

Mechanically induced silyl ester cleavage under acidic conditions investigated by AFM-based single-molecule force spectroscopy in the force-ramp mode

Reduction of Acetonitrile by Hydrated Magnesium Cations Mg + (H 2 O) n (n ≈20–60) in the Gas Phase

Reactions of Hydrated Singly Charged First‐Row Transition‐Metal Ions M + (H 2 O) n (M=V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) toward Nitric Oxide in the Gas Phase

Gas‐Phase Reactions of Cationic Vanadium‐Phosphorus Oxide Clusters with C 2 H x (x= 4, 6): A DFT‐Based Analysis of Reactivity Patterns

ChemInform Abstract: Reactions of Hydrated Singly Charged First‐Row Transition‐Metal Ions M + (H 2 O) n (M: V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) Toward Nitric Oxide in the Gas Phase.

Carboxylierung von Methylacrylat durch das Kohlendioxid‐Radikalanion in Wasserclustern †

Innentitelbild: Carboxylierung von Methylacrylat durch das Kohlendioxid‐Radikalanion in Wasserclustern (Angew. Chem. 35/2013)

Carboxylation of Methyl Acrylate by Carbon Dioxide Radical Anions in Gas‐Phase Water Clusters †

Inside Cover: Carboxylation of Methyl Acrylate by Carbon Dioxide Radical Anions in Gas‐Phase Water Clusters (Angew. Chem. Int. Ed. 35/2013)

Über die Rolle von (CuO) + bei spinselektiven Wasserstoff‐ und Sauerstoff‐Übertragungen in der Aktivierung von Methan †

Rücktitelbild: Über die Rolle von (CuO) + bei spinselektiven Wasserstoff‐ und Sauerstoff‐Übertragungen in der Aktivierung von Methan (Angew. Chem. 21/2011)

Darstellung, Reaktivität gegenüber Kohlenwasserstoffen und elektronische Struktur von heteronuclearen Vanadium‐Phosphor‐Sauerstoff‐Clusterionen †

Diatomic (CuO) + and Its Role in the Spin‐Selective Hydrogen‐ and Oxygen‐Atom Transfers in the Thermal Activation of Methane †

Back Cover: Diatomic (CuO) + and Its Role in the Spin‐Selective Hydrogen‐ and Oxygen‐Atom Transfers in the Thermal Activation of Methane (Angew. Chem. Int. Ed. 21/2011)

Generation, Reactivity Towards Hydrocarbons, and Electronic Structure of Heteronuclear Vanadium Phosphorous Oxygen Cluster Ions †

Mechanically activated rupture of single covalent bonds: evidence of force induced bond hydrolysis.

Selective Formic Acid Synthesis from Nanoscale Electrochemistry †

Selective Formic Acid Synthesis from Nanoscale Electrochemistry †

ChemInform Abstract: Thermal N—H Bond Activation on Anionic and Cationic Platinum Clusters: Non‐Predetermined Reaction Pathways Indicate Transitions to a Bulk Surface Reactivity.