Intramolecular electron transfer (IET) between a redox‐active organic ligand and a metal in a complex is of fundamental interest and used in a variety of applications. In this work it is demonstrated that secondary coordination sphere motifs can be applied to trigger a radical change in the electronic structure of copper complexes with a redox‐active guanidine ligand through ligand–metal IET. Hence, crown ether functions attached to the ligand allow the manipulation of the degree of IET between the guanidine ligand and the copper atom through metal encapsulation.

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Asymmetric optical multimode splitters based on optical waveguides were fabricated in glass substrates using a field-assisted ion exchange process. Accompanying simulations, conducted to study the light propagation, revealed the possibility to realize asymmetric splitters based on waveguides with different width. In the exchange process, broad mask openings in the blocking layer are compared to those consisting of closely spaced parallel lines with various widths. The waveguide profiles of the resulting splitters were recorded and the optical losses and splitting ratios were determined for a wavelength of 850 nm. Additionally data transmission tests were conducted and showed the suitability of the splitters for a bandwidth of 28 GBit/s.

Invited for the cover of this issue is the group of Hans‐Jörg Himmel at Ruprecht‐Karls‐Universität Heidelberg. The image depicts the electron transfer process using copper complexes with redox‐active guanidines. Read the full text of the article at 10.1002/chem.202003469.