Friedrich Alexandra
0000-0002-1411-7336
Julius-Maximilians-Universität Würzburg
15 papers found
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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)
Thermodynamic equilibrium between locally excited and charge-transfer states through thermally activated charge transfer in 1-(pyren-2′-yl)-o-carborane
Bithiophene‐Cored,mono‐,bis‐, andtris‐(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
Frontispiece: Bis(phenylethynyl)arene Linkers in Tetracationic Bis‐triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs
Bis(phenylethynyl)arene Linkers in Tetracationic Bis‐triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs
Role of Intermolecular Interactions in the Excited State Photophysics of Tetracene and 2,2’-Ditetracene
Persistent Room Temperature Phosphorescence from Triarylboranes: A Combined Experimental and Theoretical Study
Tetracationic Bis‐Triarylborane 1,3‐Butadiyne as a Combined Fluorimetric and Raman Probe for Simultaneous and Selective Sensing of Various DNA, RNA, and Proteins
Frontispiece: Triarylborane‐Based Helical Donor–Acceptor Compounds: Synthesis, Photophysical, and Electronic Properties
Triarylborane‐Based Helical Donor–Acceptor Compounds: Synthesis, Photophysical, and Electronic Properties
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)
Tetrabromtetraazapentacen: erhöhte Elektronenbeweglichkeit
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