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Wolfram Sander

Chemiker

Name	Wolfram Sander
Ort	Bochum (Wirkungsort) Heidelberg (Geburtsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr. rer. nat.
Beruf	Chemiker (charakteristischer Beruf)
Variante	Wolfram W. Sander
Weitere Angaben	Ruhr-Universität Bochum, Fakultät für Chemie und Biochemie, Organische Chemie II
Datensatztyp	Person
GND-Nummer	14314622X
Datensatz-ID	14314622X
Beteiligt an alle anzeigen Vibrational Circular Dichroism of a Chiral Triplet Nitrene Investigated Under Matrix‐Isolation Conditions in Parahydrogen Heavy‐Atom Tunneling in Bicyclo (4.1.0) hepta‐2,4,6‐trienes Heavy‐Atom Tunneling in Bicyclo (4.1.0) hepta‐2,4,6‐trienes Surface Diffusion Aided by a Chirality Change of Self‐Assembled Oligomers under 2D Confinement Surface Diffusion Aided by a Chirality Change of Self‐Assembled Oligomers under 2D Confinement Sequential Hydrogen Tunneling in o ‐Tolylmethylene Frontispiece: Molecular Magnets: The Synthesis and Characterization of High‐Spin Nitrenes Competitive solvent-molecule interactions govern primary processes of diphenylcarbene in solvent mixtures Sequential hydrogen tunneling in o-tolylmethylene Heavy‐Atom Tunneling in Semibullvalenes: How Driving Force, Substituents, and Environment Influence the Tunneling Rates Heavy‐Atom Tunneling in Semibullvalenes: How Driving Force, Substituents, and Environment Influence the Tunneling Rates Front Cover: Heavy‐Atom Tunneling in Semibullvalenes: How Driving Force, Substituents, and Environment Influence the Tunneling Rates (Chem. Eur. J. 46/2020) The Mystery of the Benzene‐Oxide/Oxepin Equilibrium—Heavy‐Atom Tunneling Reversed by Solvent Interactions Frontispiece: The Mystery of the Benzene‐Oxide/Oxepin Equilibrium—Heavy‐Atom Tunneling Reversed by Solvent Interactions Heavy-atom tunneling in semibullvalenes : How driving force, substituents, and environment influence the tunneling rates Investigating quantum mechanical tunneling in semibullvalenes and reactive intermediates by matrix isolation Molecular magnets : The synthesis and characterization of high-spin nitrenes The mystery of the benzene-oxide/oxepin equilibrium Solvent‐Enhanced Conformational Flexibility of Cyclic Tetrapeptides Solvent‐Enhanced Conformational Flexibility of Cyclic Tetrapeptides Front Cover: Solvent‐Enhanced Conformational Flexibility of Cyclic Tetrapeptides (ChemPhysChem 13/2019) Rücktitelbild: Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene (Angew. Chem. 42/2019) Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene Persistent Organic High‐Spin Trinitrenes Innentitelbild: Persistent Organic High‐Spin Trinitrenes (Angew. Chem. 37/2019) Back Cover: Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene (Angew. Chem. Int. Ed. 42/2019) Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene Persistent Organic High‐Spin Trinitrenes Inside Cover: Persistent Organic High‐Spin Trinitrenes (Angew. Chem. Int. Ed. 37/2019) Matrix isolation study of aryl and cyclopentadienyl carbenes Persistent organic high-spin trinitrenes Light-controlled switching of the spin state of iron(III) Activation of Molecular Hydrogen by Arylcarbenes Reactions of Arylcarbenes with Lewis Acids Imaging the Solvation of a One‐Dimensional Solid on the Molecular Scale Imaging the Solvation of a One‐Dimensional Solid on the Molecular Scale Carbenes and nitrenes in reactive matrices High-spin nitrenes Über die Abbildung von Solvat-Solvens-Wechselwirkungen zwischen funktionalisierten organischen Molekülen und Wasser auf molekularer Ebene Lösungsmittelmoleküle als Reaktionshelfer The Cope Rearrangement of 1,5‐Dimethylsemibullvalene‐2 (4)‐d 1: Experimental Evidence for Heavy‐Atom Tunneling Activation of the B−F Bond by Diphenylcarbene: A Reversible 1,2‐Fluorine Migration between Boron and Carbon The Cope Rearrangement of 1,5‐Dimethylsemibullvalene‐2 (4)‐d 1: Experimental Evidence for Heavy‐Atom Tunneling Activation of the B−F Bond by Diphenylcarbene: A Reversible 1,2‐Fluorine Migration between Boron and Carbon Inside Back Cover: Azulenylcarbenes: Rearrangements on the C 11 H 8 Potential Energy Surface (Chem. Eur. J. 35/2016) Azulenylcarbenes: Rearrangements on the C 11 H 8 Potential Energy Surface ChemInform Abstract: Nitreno Radicals Activation of Molecular Hydrogen by a Singlet Carbene through Quantum Mechanical Tunneling † The Fluorenyl Cation † Titelbild: The Fluorenyl Cation (Angew. Chem. 9/2015) Activation of Molecular Hydrogen by a Singlet Carbene through Quantum Mechanical Tunneling † The Fluorenyl Cation † Cover Picture: The Fluorenyl Cation (Angew. Chem. Int. Ed. 9/2015) The Benzylperoxyl Radical as a Source of Hydroxyl and Phenyl Radicals Deuterium and Hydrogen Tunneling in the Hydrogenation of 4‐Oxocyclohexa‐2,5‐dienylidene Hydrogen Bonding Switches the Spin State of Diphenylcarbene from Triplet to Singlet † Hydrogen Bonding Switches the Spin State of Diphenylcarbene from Triplet to Singlet † Elusive Fluoro Sulfinyl Nitrite, FS (O) NO, Produced by Photolysis of Matrix‐isolated FS (O) 2 N † Matrix Isolation and Spectroscopic Characterization of 2,5,6‐Trifluoropyridylnitren‐3‐yl EPR Studies on Branched High‐Spin Arylnitrenes

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Katalog der Deutschen Nationalbibliothek

Wolfram Sander

Vibrational Circular Dichroism of a Chiral Triplet Nitrene Investigated Under Matrix‐Isolation Conditions in Parahydrogen

Heavy‐Atom Tunneling in Bicyclo (4.1.0) hepta‐2,4,6‐trienes

Heavy‐Atom Tunneling in Bicyclo (4.1.0) hepta‐2,4,6‐trienes

Surface Diffusion Aided by a Chirality Change of Self‐Assembled Oligomers under 2D Confinement

Surface Diffusion Aided by a Chirality Change of Self‐Assembled Oligomers under 2D Confinement

Sequential Hydrogen Tunneling in o ‐Tolylmethylene

Frontispiece: Molecular Magnets: The Synthesis and Characterization of High‐Spin Nitrenes

Competitive solvent-molecule interactions govern primary processes of diphenylcarbene in solvent mixtures

Sequential hydrogen tunneling in o-tolylmethylene

Heavy‐Atom Tunneling in Semibullvalenes: How Driving Force, Substituents, and Environment Influence the Tunneling Rates

Heavy‐Atom Tunneling in Semibullvalenes: How Driving Force, Substituents, and Environment Influence the Tunneling Rates

Front Cover: Heavy‐Atom Tunneling in Semibullvalenes: How Driving Force, Substituents, and Environment Influence the Tunneling Rates (Chem. Eur. J. 46/2020)

The Mystery of the Benzene‐Oxide/Oxepin Equilibrium—Heavy‐Atom Tunneling Reversed by Solvent Interactions

Frontispiece: The Mystery of the Benzene‐Oxide/Oxepin Equilibrium—Heavy‐Atom Tunneling Reversed by Solvent Interactions

Heavy-atom tunneling in semibullvalenes : How driving force, substituents, and environment influence the tunneling rates

Investigating quantum mechanical tunneling in semibullvalenes and reactive intermediates by matrix isolation

Molecular magnets : The synthesis and characterization of high-spin nitrenes

The mystery of the benzene-oxide/oxepin equilibrium

Solvent‐Enhanced Conformational Flexibility of Cyclic Tetrapeptides

Solvent‐Enhanced Conformational Flexibility of Cyclic Tetrapeptides

Front Cover: Solvent‐Enhanced Conformational Flexibility of Cyclic Tetrapeptides (ChemPhysChem 13/2019)

Rücktitelbild: Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene (Angew. Chem. 42/2019)

Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene

Persistent Organic High‐Spin Trinitrenes

Innentitelbild: Persistent Organic High‐Spin Trinitrenes (Angew. Chem. 37/2019)

Back Cover: Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene (Angew. Chem. Int. Ed. 42/2019)

Conformational Spin Switching and Spin‐Selective Hydrogenation of a Magnetically Bistable Carbene

Persistent Organic High‐Spin Trinitrenes

Inside Cover: Persistent Organic High‐Spin Trinitrenes (Angew. Chem. Int. Ed. 37/2019)

Matrix isolation study of aryl and cyclopentadienyl carbenes

Persistent organic high-spin trinitrenes

Light-controlled switching of the spin state of iron(III)

Activation of Molecular Hydrogen by Arylcarbenes

Reactions of Arylcarbenes with Lewis Acids

Imaging the Solvation of a One‐Dimensional Solid on the Molecular Scale

Imaging the Solvation of a One‐Dimensional Solid on the Molecular Scale

Carbenes and nitrenes in reactive matrices

High-spin nitrenes

Über die Abbildung von Solvat-Solvens-Wechselwirkungen zwischen funktionalisierten organischen Molekülen und Wasser auf molekularer Ebene

Lösungsmittelmoleküle als Reaktionshelfer

The Cope Rearrangement of 1,5‐Dimethylsemibullvalene‐2 (4)‐d 1: Experimental Evidence for Heavy‐Atom Tunneling

Activation of the B−F Bond by Diphenylcarbene: A Reversible 1,2‐Fluorine Migration between Boron and Carbon

The Cope Rearrangement of 1,5‐Dimethylsemibullvalene‐2 (4)‐d 1: Experimental Evidence for Heavy‐Atom Tunneling

Activation of the B−F Bond by Diphenylcarbene: A Reversible 1,2‐Fluorine Migration between Boron and Carbon

Inside Back Cover: Azulenylcarbenes: Rearrangements on the C 11 H 8 Potential Energy Surface (Chem. Eur. J. 35/2016)

Azulenylcarbenes: Rearrangements on the C 11 H 8 Potential Energy Surface

ChemInform Abstract: Nitreno Radicals

Activation of Molecular Hydrogen by a Singlet Carbene through Quantum Mechanical Tunneling †

The Fluorenyl Cation †

Titelbild: The Fluorenyl Cation (Angew. Chem. 9/2015)

Activation of Molecular Hydrogen by a Singlet Carbene through Quantum Mechanical Tunneling †

The Fluorenyl Cation †

Cover Picture: The Fluorenyl Cation (Angew. Chem. Int. Ed. 9/2015)

The Benzylperoxyl Radical as a Source of Hydroxyl and Phenyl Radicals

Deuterium and Hydrogen Tunneling in the Hydrogenation of 4‐Oxocyclohexa‐2,5‐dienylidene

Hydrogen Bonding Switches the Spin State of Diphenylcarbene from Triplet to Singlet †

Hydrogen Bonding Switches the Spin State of Diphenylcarbene from Triplet to Singlet †

Elusive Fluoro Sulfinyl Nitrite, FS (O) NO, Produced by Photolysis of Matrix‐isolated FS (O) 2 N †

Matrix Isolation and Spectroscopic Characterization of 2,5,6‐Trifluoropyridylnitren‐3‐yl

EPR Studies on Branched High‐Spin Arylnitrenes