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Matthias Ferger

Chemiker

Name	Matthias Ferger
Zeit	2019- (Wirkungsdaten)
Ort	Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr.
Beruf	Chemiker (charakteristischer Beruf)
Weitere Angaben	Dissertation an der Fakultät für Chemie und Pharmazie / Institut für Anorganische Chemie der Univ. Würzburg (2021)
Quelle	Development of New Methods for Triarylborane Synthesis and Investigation of Triarylborane Chromophores for DNA and RNA Sensing and Singlet Oxygen Sensitization - 2023
Datensatztyp	Person
GND-Nummer	1292596821
Datensatz-ID	1292596821
Beteiligt an alle anzeigen Development of New Methods for Triarylborane Synthesis and Investigation of Triarylborane Chromophores for DNA and RNA Sensing and Singlet Oxygen Sensitization Electron‐Rich EDOT Linkers in Tetracationic bis‐Triarylborane Chromophores: Influence on Water Stability, Biomacromolecule Sensing, and Photoinduced Cytotoxicity Methyl Viologens of Bis‐(4’‐Pyridylethynyl)Arenes – Structures, Photophysical and Electrochemical Studies, and their Potential Application in Biology Pure Boric Acid Does Not Show Room-Temperature Phosphorescence (RTP) Electron‐Rich EDOT Linkers in Tetracationic bis‐Triarylborane Chromophores: Influence on Water Stability, Biomacromolecule Sensing, and Photoinduced Cytotoxicity Methyl Viologens of Bis‐(4’‐Pyridylethynyl) Arenes – Structures, Photophysical and Electrochemical Studies, and their Potential Application in Biology Pure Boric Acid Does Not Show Room‐Temperature Phosphorescence (RTP) Pure Boric Acid Does Not Show Room‐Temperature Phosphorescence (RTP) Bis(phenylethynyl)arene Linkers in Tetracationic Bis-triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs Bithiophene-Cored, mono-, bis-, and tris-(Trimethylammonium)-Substituted, bis-Triarylborane Chromophores: Effect of the Number and Position of Charges on Cell Imaging and DNA/RNA Sensing Synthesis of Highly Functionalizable Symmetrically and Unsymmetrically Substituted Triarylboranes from Bench-Stable Boron Precursors Bithiophene‐Cored, mono‐ , bis‐ , and tris‐ (Trimethylammonium)‐Substituted, bis‐ Triarylborane Chromophores: Effect of the Number and Position of Charges on Cell Imaging and DNA/RNA Sensing Synthesis of Highly Functionalizable Symmetrically and Unsymmetrically Substituted Triarylboranes from Bench‐Stable Boron Precursors Bis(phenylethynyl)arene Linkers in Tetracationic Bis‐triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs Synthetic Approaches to Triarylboranes from 1885 to 2020 Frontispiece: Synthetic Approaches to Triarylboranes from 1885 to 2020 Frontispiece: Bis(phenylethynyl)arene Linkers in Tetracationic Bis‐triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs Synthetic Approaches to Triarylboranes from 1885 to 2020 Tetracationic Bis‐Triarylborane 1,3‐Butadiyne as a Combined Fluorimetric and Raman Probe for Simultaneous and Selective Sensing of Various DNA, RNA, and Proteins Optimization of Aqueous Stability versus π‐Conjugation in Tetracationic Bis (triarylborane) Chromophores: Applications in Live‐Cell Fluorescence Imaging Cover Feature: Optimization of Aqueous Stability versus π‐Conjugation in Tetracationic Bis (triarylborane) Chromophores: Applications in Live‐Cell Fluorescence Imaging (Chem. Eur. J. 32/2019)

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Katalog der Deutschen Nationalbibliothek

Matthias Ferger

Development of New Methods for Triarylborane Synthesis and Investigation of Triarylborane Chromophores for DNA and RNA Sensing and Singlet Oxygen Sensitization

Electron‐Rich EDOT Linkers in Tetracationic bis‐Triarylborane Chromophores: Influence on Water Stability, Biomacromolecule Sensing, and Photoinduced Cytotoxicity

Methyl Viologens of Bis‐(4’‐Pyridylethynyl)Arenes – Structures, Photophysical and Electrochemical Studies, and their Potential Application in Biology

Pure Boric Acid Does Not Show Room-Temperature Phosphorescence (RTP)

Electron‐Rich EDOT Linkers in Tetracationic bis‐Triarylborane Chromophores: Influence on Water Stability, Biomacromolecule Sensing, and Photoinduced Cytotoxicity

Methyl Viologens of Bis‐(4’‐Pyridylethynyl) Arenes – Structures, Photophysical and Electrochemical Studies, and their Potential Application in Biology

Pure Boric Acid Does Not Show Room‐Temperature Phosphorescence (RTP)

Pure Boric Acid Does Not Show Room‐Temperature Phosphorescence (RTP)

Bis(phenylethynyl)arene Linkers in Tetracationic Bis-triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs

Bithiophene-Cored, mono-, bis-, and tris-(Trimethylammonium)-Substituted, bis-Triarylborane Chromophores: Effect of the Number and Position of Charges on Cell Imaging and DNA/RNA Sensing

Synthesis of Highly Functionalizable Symmetrically and Unsymmetrically Substituted Triarylboranes from Bench-Stable Boron Precursors

Bithiophene‐Cored, mono‐ , bis‐ , and tris‐ (Trimethylammonium)‐Substituted, bis‐ Triarylborane Chromophores: Effect of the Number and Position of Charges on Cell Imaging and DNA/RNA Sensing

Synthesis of Highly Functionalizable Symmetrically and Unsymmetrically Substituted Triarylboranes from Bench‐Stable Boron Precursors

Bis(phenylethynyl)arene Linkers in Tetracationic Bis‐triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs

Synthetic Approaches to Triarylboranes from 1885 to 2020

Frontispiece: Synthetic Approaches to Triarylboranes from 1885 to 2020

Frontispiece: Bis(phenylethynyl)arene Linkers in Tetracationic Bis‐triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs

Synthetic Approaches to Triarylboranes from 1885 to 2020

Tetracationic Bis‐Triarylborane 1,3‐Butadiyne as a Combined Fluorimetric and Raman Probe for Simultaneous and Selective Sensing of Various DNA, RNA, and Proteins

Optimization of Aqueous Stability versus π‐Conjugation in Tetracationic Bis (triarylborane) Chromophores: Applications in Live‐Cell Fluorescence Imaging

Cover Feature: Optimization of Aqueous Stability versus π‐Conjugation in Tetracationic Bis (triarylborane) Chromophores: Applications in Live‐Cell Fluorescence Imaging (Chem. Eur. J. 32/2019)