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Martin K. Beyer (1969-)

Physiker

Name	Martin K. Beyer
Zeit	1969- (Lebensdaten)
Ort	Ingolstadt (Geburtsort) Kiel (Wirkungsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Physiker (charakteristischer Beruf)
Variante	M. K. Beyer Martin Beyer
Beziehung	Christian-Albrechts-Universität zu Kiel. Institut für Physikalische Chemie
Weitere Angaben	Diss. München 1999; Prof. für Physikalische Chemie an der Christian-Albrechts-Universität Kiel
Datensatztyp	Person
GND-Nummer	1016363753
Datensatz-ID	1016363753
Beteiligt an alle anzeigen 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 Structure and reactivity of solvated ions

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Katalog der Deutschen Nationalbibliothek

Martin K. Beyer (1969-)

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

Structure and reactivity of solvated ions