A5058244746- Crystallization and Solubility Studies
- X-ray Diffraction in Crystallography
- Radical Photochemical Reactions
- Catalytic C–H Functionalization Methods
- Fluorine in Organic Chemistry
- Surfactants and Colloidal Systems
- Advanced Photocatalysis Techniques
- Curcumin's Biomedical Applications
- Spectroscopy and Quantum Chemical Studies
- Natural product bioactivities and synthesis
- Essential Oils and Antimicrobial Activity
- Ionic liquids properties and applications
- Biochemical and biochemical processes
- nanoparticles nucleation surface interactions
- Thermodynamic properties of mixtures
- Sulfur-Based Synthesis Techniques
- Material Dynamics and Properties
- Phytochemicals and Antioxidant Activities
- Innovative Microfluidic and Catalytic Techniques Innovation
- Enzyme Catalysis and Immobilization
- Polyoxometalates: Synthesis and Applications
- Physiological and biochemical adaptations
- Field-Flow Fractionation Techniques
- Mass Spectrometry Techniques and Applications
- Dental Erosion and Treatment
University of Regensburg
2002-2023
The amino alcohol meglumine solubilizes organic compounds in water and enforces the formation of electron donor acceptor (EDA) complexes haloarenes with indoles, anilines, anisoles or thiols, which are not observed solvents. UV-A photoinduced transfer within EDA induces mesolytic cleavage halide ion radical recombination arenes leading, after rearomatization proton loss to C-C C-S coupling products. Depending on substitution pattern selective unique cross-couplings observed. UV NMR...
Salting-in or salting-out tendencies depend on a balance between headgroup-specific ion effects and the hydrophobicity of tail.
Binary mixtures of ethanol and triacetin are studied by means COSMO-RS-based calculations, DLS, SWAXS, DRS. The findings related to the significant solubility (tetrahydro)curcumin in these mixtures.
Abstract The amino alcohol meglumine solubilizes organic compounds in water and enforces the formation of electron donor acceptor (EDA) complexes haloarenes with indoles, anilines, anisoles or thiols, which are not observed solvents. UV‐A photoinduced transfer within EDA induces mesolytic cleavage halide ion radical recombination arenes leading, after rearomatization proton loss to C−C C−S coupling products. Depending on substitution pattern selective unique cross‐couplings observed. UV NMR...
Graphical Abstract The sugar alcohol meglumine enhances the solubility of organic compounds in water and enforces formation electron donor–acceptor (EDA) complexes, enabling photochemical C−C C−S cross-coupling transformations without sensitizers. light-driven redox-neutral protocol connects haloarenes with indoles, anilines, anisoles, thiols, as reported by Burkhard König co-workers their Research Article (e202218775).