| Literature DB >> 31210369 |
Lucas Ueberricke1, Daniel Holub2, Julian Kranz2, Frank Rominger1, Marcus Elstner2, Michael Mastalerz1.
Abstract
Triptycene end-capped quinoxalinophenanthrophenazine reveals a coplanar arrangement with a high overlap of the π planes. Four structurally related model compounds bearing electron-withdrawing or -donating groups were synthesized, and their optoelectronic properties were characterized by using cyclovoltammetry, absorption- and emission spectroscopy as well as theoretical calculations. The directional robustness of the triptycene end-capping of these compounds was tested by using single-crystal X-ray diffraction. The impact of solvents and crystallization conditions has also been investigated. In total, 17 single-crystal structures were obtained. Each structure was evaluated for its potential charge-transfer capability taking into account the overall molecular packing, solvent enclathration and the structural overlap of the π planes of adjacent molecules. For this purpose, charge-transfer integrals were also calculated for every π-stacked dimer.Entities:
Keywords: charge transfer; crystal engineering; heteroacenes; triptycenes; π stacking
Year: 2019 PMID: 31210369 DOI: 10.1002/chem.201902002
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236