| Literature DB >> 26013642 |
Volker Strauss1, Johannes T Margraf1,2, Konstantin Dirian1, Zois Syrgiannis3, Maurizio Prato3, Cordula Wessendorf1, Andreas Hirsch1, Timothy Clark2, Dirk M Guldi4.
Abstract
We describe the formation of charge-transfer complexes that feature electron-donating carbon nanodots (CND) and electron-accepting perylenediimides (PDI). The functionalities of PDIs have been selected to complement those of CNDs in terms of electrostatic and π-stacking interactions based on oppositely charged ionic head groups and extended π-systems, respectively. Importantly, the contributions from electrostatic interactions were confirmed in reference experiments, in which stronger interactions were found for PDIs that feature positively rather than negatively charged head groups. The electronic interactions between the components in the ground and excited state were characterized in complementary absorption and fluorescence titration assays that suggest charge-transfer interactions in both states with binding constants on the order of 8×10(4) M(-1) (25 L g(-1) ). Selective excitation of the two components in ultrafast pump probe experiments gave a 210 ps lived charge-separated state.Entities:
Keywords: carbon nanodots; charge transfer; donor-acceptor compounds; perylenediimides; transient absorption
Year: 2015 PMID: 26013642 DOI: 10.1002/anie.201502482
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336