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Anne Staubitz

Chemikerin

Name	Anne Staubitz
Place	Kiel (Wirkungsort) Deutschland
Gender	weiblich
Academic degree	Prof. Dr.
Profession	Chemikerin (characteristic profession) Hochschullehrerin
Variant	Anne C. Staubitz A. Staubitz
Related	Christian-Albrechts-Universität zu Kiel. Institut für Organische Chemie
Record type	Person
GND-Identifier	1032749865
Record ID	1032749865
Involved in show all Bistable Dual‐Responsive Azobenzene‐co‐PNIPAM Soft Microactuators via Two‐Photon Direct Laser Writing Bistable Dual‐Responsive Azobenzene‐co‐PNIPAM Soft Microactuators via Two‐Photon Direct Laser Writing Dehydrocoupling of Phosphine‐Borane Adducts Under Ambient Conditions Using Aminoboranes as Hydrogen Acceptors Light and strain responsive polymeric materials Nanoporous Au/Ag Catalyzed Benzylic sp 3 C−H Oxidation of 9H‐Fluorene Derivatives and Similar Molecules with TBHP Centennial Isomers: A Unique Fluorinated Azobenzene Macrocyclus with Dual Stability Over 120 Years Kinetic stabilization of low valent main group compounds : Kinetische Stabilisierung von niedervalenten Hauptgruppen-Verbindungen Light Actuation: from synthesis to material A Photomechanical Film in which Liquid Crystal Design Shifts the Absorption into the Visible Light Range Modification of Azobenzene based switches Nanoporous Gold: From structure evolution to functional properties in catalysis and electrochemistry Organic photosensitizers for light-driven hydrogen evolution : synthesis, characterization and application Small molecule activation mediated by metal ligand cooperation via a dearomatization/rearomatization reaction sequence using redox active pyridine based ligand-systems in transition metal complexes : Aktivierung kleiner Moleküle mittels Metall-Ligand-Kooperation über eine dearomatisierungs/rearomatisierungs Reaktions-Sequenz mit redoxaktiven pyridinbasierenden Liganden-Systemen in Übergangsmetall-Komplexen Synthesis and characterization of diazocines and their Incorporation in polymers The Influence of 1,2-Boron-Nitrogen Substitutions on the Properties of Polycyclic Aromatic Hydrocarbons Azaborinine : Hybride aus Benzol und Borazin A Co-Polymerizable Linker for the Covalent Attachment of Fibronectin Makes pHEMA Hydrogels Cell-Adhesive Functional Nanomaterials for Environmentally Friendly Biofouling Control Ein nanoporöser Goldschwamm als Katalysator : Nanomaterialien Modification of Azobenzenes by Cross-Coupling Reactions Functionalization of nanoporous gold with macrocyclic metal complexes: a novel class of heterogeneous singlet oxygen photosensitizers Stannoles – unseen heterocycles with unique optoelectronic properties : Stannole – Nicht-gesehene Heterozyklen mit einzigartigen optoelektronischen Eigenschaften Synthesis and characterization of main group elements in organic structures π-Conjugated stannole copolymers synthesised by a tin-selective Stille cross-coupling reaction Novel ESIPT-based luminophores – synthesis and characterization : Neuartige ESIPT-basierte Luminophore – Synthese und Charakterisierung Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes Cover Feature: Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes (Chem. Eur. J. 58/2019) Living Materials Herald a New Era in Soft Robotics Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes Photo- and Mechanoresponsive Polymeric Systems Synthesis, Structure, Thermal Behavior and cis/trans Isomerization of 2,2'-(EMe₃)₂ (E = C, Si, Ge, Sn) Substituted Azobenzenes Syntheses and Properties of Tin‐Containing Conjugated Heterocycles Frontispiece: Syntheses and Properties of Tin‐Containing Conjugated Heterocycles Hochmolekulare Polymere mit diversen Substituenten durch eine ungewöhnliche, metallfreie Synthese von Poly (aminoboranen) Syntheses of Azaborine Polymers and Optimisation of Precursor Syntheses Nucleophile‐Selective Cross‐Coupling Reactions with Vinyl and Alkynyl Bromides on a Dinucleophilic Aromatic Substrate ChemInform Abstract: High‐Yield Lithiation of Azobenzenes by Tin—Lithium Exchange. ChemInform Abstract: Nucleophile‐Selective Cross‐Coupling Reactions with Vinyl and Alkynyl Bromides on a Dinucleophilic Aromatic Substrate. Challenges and Solutions for Joining Polymer Materials ChemInform Abstract: Tin‐Functionalized Azobenzenes as Nucleophiles in Stille Cross‐Coupling Reactions. ChemInform Abstract: Dual Selectivity: Electrophile and Nucleophile Selective Cross‐Coupling Reactions on a Single Aromatic Substrate. Highly Tin‐Selective Stille Coupling: Synthesis of a Polymer Containing a Stannole in the Main Chain † “Spontaneous” Ambient Temperature Dehydrocoupling of Aromatic Amine–Boranes Joining the Un‐Joinable: Adhesion Between Low Surface Energy Polymers Using Tetrapodal ZnO Linkers Scope and Selectivity of Heterogeneous Rh 0 ‐Catalyzed Tandem Dehydrocoupling/Hydrogenation Using Me 2 NH·BH 3 as a Stoichiometric H 2 Source Experimental and Theoretical Studies of the Potential Interconversion of the Amine–Borane i Pr 2 NH·BH (C 6 F 5) 2 and the Aminoborane i Pr 2 N=B (C 6 F 5) 2 Involving Hydrogen Loss and Uptake ChemInform Abstract: Ammonia‐Borane and Related Compounds as Dihydrogen Sources ChemInform Abstract: Amine‐ and Phosphine‐orane Adducts: New Interest in Old Molecules Iridium‐Catalyzed Dehydrocoupling of Primary Amine–Borane Adducts: A Route to High Molecular Weight Polyaminoboranes, Boron–Nitrogen Analogues of Polyolefins † Iridium‐Catalyzed Dehydrocoupling of Primary Amine–Borane Adducts: A Route to High Molecular Weight Polyaminoboranes, Boron–Nitrogen Analogues of Polyolefins †

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Katalog der Deutschen Nationalbibliothek

Anne Staubitz

Bistable Dual‐Responsive Azobenzene‐co‐PNIPAM Soft Microactuators via Two‐Photon Direct Laser Writing

Bistable Dual‐Responsive Azobenzene‐co‐PNIPAM Soft Microactuators via Two‐Photon Direct Laser Writing

Dehydrocoupling of Phosphine‐Borane Adducts Under Ambient Conditions Using Aminoboranes as Hydrogen Acceptors

Light and strain responsive polymeric materials

Nanoporous Au/Ag Catalyzed Benzylic sp 3 C−H Oxidation of 9H‐Fluorene Derivatives and Similar Molecules with TBHP

Centennial Isomers: A Unique Fluorinated Azobenzene Macrocyclus with Dual Stability Over 120 Years

Kinetic stabilization of low valent main group compounds : Kinetische Stabilisierung von niedervalenten Hauptgruppen-Verbindungen

Light Actuation: from synthesis to material

A Photomechanical Film in which Liquid Crystal Design Shifts the Absorption into the Visible Light Range

Modification of Azobenzene based switches

Nanoporous Gold: From structure evolution to functional properties in catalysis and electrochemistry

Organic photosensitizers for light-driven hydrogen evolution : synthesis, characterization and application

Synthesis and characterization of diazocines and their Incorporation in polymers

The Influence of 1,2-Boron-Nitrogen Substitutions on the Properties of Polycyclic Aromatic Hydrocarbons

Azaborinine : Hybride aus Benzol und Borazin

A Co-Polymerizable Linker for the Covalent Attachment of Fibronectin Makes pHEMA Hydrogels Cell-Adhesive

Functional Nanomaterials for Environmentally Friendly Biofouling Control

Ein nanoporöser Goldschwamm als Katalysator : Nanomaterialien

Modification of Azobenzenes by Cross-Coupling Reactions

Functionalization of nanoporous gold with macrocyclic metal complexes: a novel class of heterogeneous singlet oxygen photosensitizers

Stannoles – unseen heterocycles with unique optoelectronic properties : Stannole – Nicht-gesehene Heterozyklen mit einzigartigen optoelektronischen Eigenschaften

Synthesis and characterization of main group elements in organic structures

π-Conjugated stannole copolymers synthesised by a tin-selective Stille cross-coupling reaction

Novel ESIPT-based luminophores – synthesis and characterization : Neuartige ESIPT-basierte Luminophore – Synthese und Charakterisierung

Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes

Cover Feature: Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes (Chem. Eur. J. 58/2019)

Living Materials Herald a New Era in Soft Robotics

Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes

Photo- and Mechanoresponsive Polymeric Systems

Synthesis, Structure, Thermal Behavior and cis/trans Isomerization of 2,2'-(EMe₃)₂ (E = C, Si, Ge, Sn) Substituted Azobenzenes

Syntheses and Properties of Tin‐Containing Conjugated Heterocycles

Frontispiece: Syntheses and Properties of Tin‐Containing Conjugated Heterocycles

Hochmolekulare Polymere mit diversen Substituenten durch eine ungewöhnliche, metallfreie Synthese von Poly (aminoboranen)

Syntheses of Azaborine Polymers and Optimisation of Precursor Syntheses

Nucleophile‐Selective Cross‐Coupling Reactions with Vinyl and Alkynyl Bromides on a Dinucleophilic Aromatic Substrate

ChemInform Abstract: High‐Yield Lithiation of Azobenzenes by Tin—Lithium Exchange.

ChemInform Abstract: Nucleophile‐Selective Cross‐Coupling Reactions with Vinyl and Alkynyl Bromides on a Dinucleophilic Aromatic Substrate.

Challenges and Solutions for Joining Polymer Materials

ChemInform Abstract: Tin‐Functionalized Azobenzenes as Nucleophiles in Stille Cross‐Coupling Reactions.

ChemInform Abstract: Dual Selectivity: Electrophile and Nucleophile Selective Cross‐Coupling Reactions on a Single Aromatic Substrate.

Highly Tin‐Selective Stille Coupling: Synthesis of a Polymer Containing a Stannole in the Main Chain †

“Spontaneous” Ambient Temperature Dehydrocoupling of Aromatic Amine–Boranes

Joining the Un‐Joinable: Adhesion Between Low Surface Energy Polymers Using Tetrapodal ZnO Linkers

Scope and Selectivity of Heterogeneous Rh 0 ‐Catalyzed Tandem Dehydrocoupling/Hydrogenation Using Me 2 NH·BH 3 as a Stoichiometric H 2 Source

Experimental and Theoretical Studies of the Potential Interconversion of the Amine–Borane i Pr 2 NH·BH (C 6 F 5) 2 and the Aminoborane i Pr 2 N=B (C 6 F 5) 2 Involving Hydrogen Loss and Uptake

ChemInform Abstract: Ammonia‐Borane and Related Compounds as Dihydrogen Sources

ChemInform Abstract: Amine‐ and Phosphine‐orane Adducts: New Interest in Old Molecules

Iridium‐Catalyzed Dehydrocoupling of Primary Amine–Borane Adducts: A Route to High Molecular Weight Polyaminoboranes, Boron–Nitrogen Analogues of Polyolefins †

Iridium‐Catalyzed Dehydrocoupling of Primary Amine–Borane Adducts: A Route to High Molecular Weight Polyaminoboranes, Boron–Nitrogen Analogues of Polyolefins †