4 results match your criteria: "Organisch-Chemisches Institut Ruprecht-Karls-Universität Heidelberg Im Neuenheimer Feld 270 69120 Heidelberg Germany.[Affiliation]"

We report the electron-beam induced crosslinking of cinnamate-substituted polythiophene proceeding excited state [2+2]-cycloaddition. Network formation in thin films is evidenced by infrared spectroscopy and film retention experiments. For the polymer studied herin, the electron-stimulated process appears to be superior to photo (UV)-induced crosslinking as it leads to less degradation.

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The variety of shape-persistent organic cages by imine bond formation has tremendously enlarged in recent years by using different building blocks (aldehydes and amines) in the condensation reactions. Here, we describe the use of a kinked tetraldehyde to generate pumpkin-shaped cages with concave walls, similar to cucurbiturils.

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The synthesis of a highly soluble triptycene end-capped indigo and its bay annulated derivative is reported. Both compounds have been studied by absorption and emission spectroscopy cyclic voltammetry, as well as theoretical calculations and compared to the parent indigo and bay annulated indigo. Besides a large improvement of solubility in organic solvents by the factor of approx.

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Article Synopsis
  • Three imine cages with tetrahedral geometry were tested for their ability to encapsulate different tetra-alkylammonium salts in various solvents.
  • In dichloromethane, the cage with the smallest window only captures NEt but not NMe, while larger cages accommodate both ions.
  • Kinetic experiments and molecular simulations were conducted to understand uptake mechanisms, and additional NMR studies were performed to explore the complexation of pharmaceutical compounds like acetylcholine and muscarine.
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