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Max M. Hansmann (1987-)

Chemiker

Name	Max M. Hansmann
Zeit	1987- (Lebensdaten)
Ort	Hamburg (Geburtsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr. rer. nat. (an der Universität Heidelberg) (2015)
Beruf	Chemiker (charakteristischer Beruf) Hochschullehrer
Variante	Max Hansmann Max Martin Hansmann
Beziehung	University of California, San Diego (Postdoktorand) (2015-2017) Organisch-Chemisches Institut (Heidelberg) (2012-2015) Technische Universität Dortmund. Organische Chemie (Professor) (2023-)
Quelle	Homepage: http://www.ccb.tu-dortmund.de/fb03/de/Forschung/OC/Hansmann/index.html (22.11.2019) Homepage: https://www.uni-goettingen.de/de/max+m.+hansmann/573687.html (22.11.2019)
Datensatztyp	Person
GND-Nummer	1025310926
Datensatz-ID	1025310926
Beteiligt an alle anzeigen From a P‐Bridging Phosphaketene to μ‐Phosphinidenide and μ‐Diphosphaurea Units at a Dinickel Core Spaltung von Carbodicarbenen mit N 2 O zu stabilen Diazoalkenen: Zweifacher Ligandenaustausch an einem C (0)‐Atom Cleavage of Carbodicarbenes with N 2 O for Accessing Stable Diazoalkenes: Two‐Fold Ligand Exchange at a C (0)‐Atom 2‐Methylene‐1,2‐dihydropyridines (2‐pyNHOs): Highly Nucleophilic Enamines Cycloadditionen von Diazoalkenen mit P 4 und t BuCP: Ein Zugang zu Diazaphospholen Cycloadditions of Diazoalkenes with P 4 and t BuCP: Access to Diazaphospholes para ‐Aminoazobenzole – Bipolare Redoxaktive Verbindungen para ‐Aminoazobenzenes—Bipolar Redox‐Active Molecules Mesoionic N‐Heterocyclic Olefins as Initiators for the Lewis Pair Polymerization of Epoxides Pyridinium‐abgeleitete mesoionische N ‐heterocyclische Olefine (py‐mNHOs) Pyridinium‐Derived Mesoionic N ‐Heterocyclic Olefins (py‐mNHOs) Self‐Assembled Monolayers of N‐Heterocyclic Olefins on Au (111) Self‐Assembled Monolayers of N‐Heterocyclic Olefins on Au (111) Mesoionische N ‐Heterocyclische Olefine verschieben die obere Grenze der Nucleophilie‐Skala Pushing the Upper Limit of Nucleophilicity Scales by Mesoionic N ‐Heterocyclic Olefins Diazoalkene – Von einem flüchtigen Intermediat zu einer neuen stabilen Substanzklasse in der Organischen Chemie Diazoalkenes: From an Elusive Intermediate to a Stable Substance Class in Organic Chemistry Raumtemperatur‐Stabile Diazoalkene mittels Diazotransfer von Aziden: Pyridin‐basierte Diazoalkene Room‐Temperature‐Stable Diazoalkenes by Diazo Transfer from Azides: Pyridine‐Derived Diazoalkenes Transition Metal‐Free Activation of Carbon Monoxide: Ketenyl Anions by PPh 3/CO Exchange Transition Metal‐Free Activation of Carbon Monoxide: Ketenyl Anions by PPh 3/CO Exchange Pushing the upper limit of nucleophilicity scales by mesoionic N‐heterocyclic olefins Organische Vier‐Elektronen Redox‐Systeme basierend auf Bipyridin‐ und Phenanthrolin‐Carben‐Architekturen Organic Four‐Electron Redox Systems Based on Bipyridine and Phenanthroline Carbene Architectures Organic four‐electron redox systems based on bipyridine and phenanthroline carbene architectures Singlet Fission in Carbene‐Derived Diradicaloids Titelbild: Singlet Fission in Carbene‐Derived Diradicaloids (Angew. Chem. 20/2020) Stable Mesoionic N‐Heterocyclic Olefins (mNHOs) Cover Picture: Singlet Fission in Carbene‐Derived Diradicaloids (Angew. Chem. Int. Ed. 20/2020) Stable Mesoionic N‐Heterocyclic Olefins (mNHOs) Singlet Fission in Carbene‐Derived Diradicaloids A μ‐Phosphido Diiron Dumbbell in Multiple Oxidation States A μ‐Phosphido Diiron Dumbbell in Multiple Oxidation States Synthesis of Azaphosphinines by Directed Inverse‐Electron‐Demand Hetero‐Diels–Alder Reactions with Na (OCP) Intercepting a Transient Phosphino‐Arsinidene Gold‐Catalyzed Formal Cyclisation/Dimerization of Thiophene‐Tethered Diynes Intramolecular anti ‐Phosphinoauration of Alkynes: An FLP‐Motivated Approach to Stable Aurated Phosphindolium Complexes New Pathways for the Dual Gold‐Catalyzed Cyclization of Diynes The Propargyl Rearrangement to Functionalised Allyl‐Boron and Borocation Compounds Erzeugung von Festkörperlumineszenz durch Koordination der Lewis‐Säure B (C 6 F 5) 3 an nicht‐emittierende Aldehyde B (C 6 F 5) 3: A Lewis Acid that Brings the Light to the Solid State Correlating the reactivity of gold and boron electrophiles Cyclisation versus 1,1‐Carboboration: Reactions of B (C 6 F 5) 3 with Propargyl Amides

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Katalog der Deutschen Nationalbibliothek

Max M. Hansmann (1987-)

From a P‐Bridging Phosphaketene to μ‐Phosphinidenide and μ‐Diphosphaurea Units at a Dinickel Core

Spaltung von Carbodicarbenen mit N 2 O zu stabilen Diazoalkenen: Zweifacher Ligandenaustausch an einem C (0)‐Atom

Cleavage of Carbodicarbenes with N 2 O for Accessing Stable Diazoalkenes: Two‐Fold Ligand Exchange at a C (0)‐Atom

2‐Methylene‐1,2‐dihydropyridines (2‐pyNHOs): Highly Nucleophilic Enamines

Cycloadditionen von Diazoalkenen mit P 4 und t BuCP: Ein Zugang zu Diazaphospholen

Cycloadditions of Diazoalkenes with P 4 and t BuCP: Access to Diazaphospholes

para ‐Aminoazobenzole – Bipolare Redoxaktive Verbindungen

para ‐Aminoazobenzenes—Bipolar Redox‐Active Molecules

Mesoionic N‐Heterocyclic Olefins as Initiators for the Lewis Pair Polymerization of Epoxides

Pyridinium‐abgeleitete mesoionische N ‐heterocyclische Olefine (py‐mNHOs)

Pyridinium‐Derived Mesoionic N ‐Heterocyclic Olefins (py‐mNHOs)

Self‐Assembled Monolayers of N‐Heterocyclic Olefins on Au (111)

Self‐Assembled Monolayers of N‐Heterocyclic Olefins on Au (111)

Mesoionische N ‐Heterocyclische Olefine verschieben die obere Grenze der Nucleophilie‐Skala

Pushing the Upper Limit of Nucleophilicity Scales by Mesoionic N ‐Heterocyclic Olefins

Diazoalkene – Von einem flüchtigen Intermediat zu einer neuen stabilen Substanzklasse in der Organischen Chemie

Diazoalkenes: From an Elusive Intermediate to a Stable Substance Class in Organic Chemistry

Raumtemperatur‐Stabile Diazoalkene mittels Diazotransfer von Aziden: Pyridin‐basierte Diazoalkene

Room‐Temperature‐Stable Diazoalkenes by Diazo Transfer from Azides: Pyridine‐Derived Diazoalkenes

Transition Metal‐Free Activation of Carbon Monoxide: Ketenyl Anions by PPh 3/CO Exchange

Transition Metal‐Free Activation of Carbon Monoxide: Ketenyl Anions by PPh 3/CO Exchange

Pushing the upper limit of nucleophilicity scales by mesoionic N‐heterocyclic olefins

Organische Vier‐Elektronen Redox‐Systeme basierend auf Bipyridin‐ und Phenanthrolin‐Carben‐Architekturen

Organic Four‐Electron Redox Systems Based on Bipyridine and Phenanthroline Carbene Architectures

Organic four‐electron redox systems based on bipyridine and phenanthroline carbene architectures

Singlet Fission in Carbene‐Derived Diradicaloids

Titelbild: Singlet Fission in Carbene‐Derived Diradicaloids (Angew. Chem. 20/2020)

Stable Mesoionic N‐Heterocyclic Olefins (mNHOs)

Cover Picture: Singlet Fission in Carbene‐Derived Diradicaloids (Angew. Chem. Int. Ed. 20/2020)

Stable Mesoionic N‐Heterocyclic Olefins (mNHOs)

Singlet Fission in Carbene‐Derived Diradicaloids

A μ‐Phosphido Diiron Dumbbell in Multiple Oxidation States

A μ‐Phosphido Diiron Dumbbell in Multiple Oxidation States

Synthesis of Azaphosphinines by Directed Inverse‐Electron‐Demand Hetero‐Diels–Alder Reactions with Na (OCP)

Intercepting a Transient Phosphino‐Arsinidene

Gold‐Catalyzed Formal Cyclisation/Dimerization of Thiophene‐Tethered Diynes

Intramolecular anti ‐Phosphinoauration of Alkynes: An FLP‐Motivated Approach to Stable Aurated Phosphindolium Complexes

New Pathways for the Dual Gold‐Catalyzed Cyclization of Diynes

The Propargyl Rearrangement to Functionalised Allyl‐Boron and Borocation Compounds

Erzeugung von Festkörperlumineszenz durch Koordination der Lewis‐Säure B (C 6 F 5) 3 an nicht‐emittierende Aldehyde

B (C 6 F 5) 3: A Lewis Acid that Brings the Light to the Solid State

Correlating the reactivity of gold and boron electrophiles

Cyclisation versus 1,1‐Carboboration: Reactions of B (C 6 F 5) 3 with Propargyl Amides