TY - JOUR A1 - Bäumer, Nils A1 - Kartha, Kalathil K. A1 - Allampally, Naveen Kumar A1 - Yagai, Shiki A1 - Albuquerque, Rodrigo Q. A1 - Fernández, Gustavo T1 - Kontrolle über Selbstassemblierung durch Ausnutzung von Koordinationsisomerie JF - Angewandte Chemie N2 - Hierin wird die inhärente geometrische Isomerie eines PtII Komplexes als neues Werkzeug zur Kontrolle von supramolekularen Assemblierungsprozessen ausgenutzt. Bestrahlung mit UV‐Licht sowie die sorgfältige Auswahl des verwendeten Lösungsmittels, der Temperatur und Konzentration führen zu einer regelbaren Koordinationsisomerie. Dies ermöglicht ein vollständig reversibles Schalten zwischen zwei definierten aggregierten Spezies (1D Fasern ↔ 2D Lamellen) mit unterschiedlichem photoresponsivem Verhalten. Unsere Erkenntnisse erweitern nicht nur die Reichweite von Koordinationsisomerie, sondern eröffnen auch aufregende Möglichkeiten zur Entwicklung neuartiger stimuliresponsiver Materialien. KW - Koordinationsisomerie KW - Photoresponsives Verhalten KW - Selbstassemblierung KW - Supramolekulare Polymere KW - π-Konjugierte Systeme Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-212176 VL - 131 IS - 44 SP - 15772 EP - 15776 ER - TY - JOUR A1 - Rest, Christina A1 - Philips, Divya Susan A1 - Dünnebacke, Torsten A1 - Sutar, Papri A1 - Sampedro, Angel A1 - Droste, Jörn A1 - Stepanenko, Vladimir A1 - Hansen, Michael Ryan A1 - Albuquerque, Rodrigo Q. A1 - Fernández, Gustavo T1 - Tuning Aqueous Supramolecular Polymerization by an Acid‐Responsive Conformational Switch JF - Chemistry – A European Journal N2 - Besides their widespread use in coordination chemistry, 2,2’‐bipyridines are known for their ability to undergo cis–trans conformational changes in response to metal ions and acids, which has been primarily investigated at the molecular level. However, the exploitation of such conformational switching in self‐assembly has remained unexplored. In this work, the use of 2,2’‐bipyridines as acid‐responsive conformational switches to tune supramolecular polymerization processes has been demonstrated. To achieve this goal, we have designed a bipyridine‐based linear bolaamphiphile, 1, that forms ordered supramolecular polymers in aqueous media through cooperative aromatic and hydrophobic interactions. Interestingly, addition of acid (TFA) induces the monoprotonation of the 2,2’‐bipyridine moiety, leading to a switch in the molecular conformation from a linear (trans) to a V‐shaped (cis) state. This increase in molecular distortion along with electrostatic repulsions of the positively charged bipyridine‐H\(^{+}\) units attenuate the aggregation tendency and induce a transformation from long fibers to shorter thinner fibers. Our findings may contribute to opening up new directions in molecular switches and stimuli‐responsive supramolecular materials. KW - acid-sensitive KW - amphiphilic systems KW - π-conjugated systems KW - noncovalent interactions KW - self-assembly Y1 - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-218118 VL - 26 IS - 44 SP - 10005 EP - 10013 ER - TY - JOUR A1 - Bäumer, Nils A1 - Kartha, Kalathil K. A1 - Kumar Allampally, Naveen A1 - Yagai, Shiki A1 - Albuquerque, Rodrigo Q. A1 - Fernández, Gustavo T1 - Exploiting Coordination Isomerism for Controlled Self-Assembly JF - Angewandte Chemie International Edition N2 - We exploited the inherent geometrical isomerism of a PtII complex as a new tool to control supramolecular assembly processes. UV irradiation and careful selection of solvent, temperature, and concentration leads to tunable coordination isomerism, which in turn allows fully reversible switching between two distinct aggregate species (1D fibers↔2D lamellae) with different photoresponsive behavior. Our findings not only broaden the scope of coordination isomerism, but also open up exciting possibilities for the development of novel stimuli-responsive nanomaterials. KW - coordination isomerism KW - photoresponsive behavior KW - self-assembly KW - supramolecular polymers KW - p-conjugated systems Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-221362 VL - 58 ER -