1 to 6 of 6 Results
Apr 16, 2024 - SFB 1249: N-Heteropolyzyklen als Funktionsmaterialien - B: Theory & Structure
Stein, Arnulf; Rolf, Daniela; Lotze, Christian; Feldmann, Sascha; Gerbert, David; Günther, Benjamin; Jeindl, Andreas; Cartus, Johannes J.; Hofmann, Oliver T.; Gade, Lutz H.; Franke, Katharina J.; Tegeder, Petra, 2024, "Electronic Properties of Tetraazaperopyrene Derivatives on Au(111): Energy-Level Alignment and Interfacial Band Formation [research data]", https://doi.org/10.11588/data/0EK2MB, heiDATA, V1
N-heteropolycyclic aromatic compounds are promising organic electron-transporting semiconductors for applications in field-effect transistors. Here, we investigated the electronic properties of 1,3,8,10-tetraazaperopyrene derivatives adsorbed on Au(111) using a complementary expe... |
Mar 4, 2024 - Blasco Group
Eichelmann, Robert; Monti, Joël; Hsu, Li-Yun; Kröger, Finn; Ballmann, Joachim; Blasco, Eva; Gade, Lutz H., 2024, "Two-Photon Microprinting of 3D Emissive Structures Using Tetraazaperylene-Derived Fluorophores [data]", https://doi.org/10.11588/data/C6UIWL, heiDATA, V1
The application of a new class of fluorophores based on a twisted tetraazaperylene core in the fabrication of emissive organic 3D microstructures has been investigated. The synthesis of a series of tetraazaperyleneamines and their corresponding octaazaperopyrenedioxides (OAPPDOs)... |
Feb 20, 2024 - Gade Group
Eichelmann, Robert; Rippel, Daniel; Ballmann, Joachim; Gade, Lutz H., 2024, "Zipping up Tetraazaperylene: Synthesis of Tetraazacoronenes via Double Coupling in the Bay Positions [data]", https://doi.org/10.11588/data/HIERR9, heiDATA, V1
Substituted tetraazacoronene fluorophores have been obtained selectively by double Suzuki–Miyaura cross coupling of symmetrically substituted 1,2-bis(pinacolatoboryl)alkenes with a bay-substituted octaazaperopyrenedioxide (OAPPDO). Subsequent Scholl reaction of the dimethoxypheny... |
Feb 20, 2024 - Gade Group
Eichelmann, Robert; Jeudy, Pierre; Schneider, Lars; Zerhoch, Jonathan; Mayer, Paula R.; Ballmann, Joachim; Deschler, Felix; Gade, Lutz H., 2024, "Chiral Bay-Alkynylated Tetraazaperylenes: Photophysics and Chiroptical Properties", https://doi.org/10.11588/data/PGSVXO, heiDATA, V1
Fully bay-alkynylated octaazaperopyrene dioxide (OAPPDO) derivatives were accessible through Stille cross coupling reaction of the corresponding bay-chlorinated derivatives. This steric congestion of the bay area led to helically chiral fluorophores, and chiral resolution of two... |
Feb 20, 2024 - Gade Group
Eichelmann, Robert; Ballmann, Joachim; Gade, Lutz H., 2024, "Tetraazacoronenes and Their Dimers, Trimers and Tetramers [data]", https://doi.org/10.11588/data/ZT3AHN, heiDATA, V1
Tetraazacoronenes were synthesized from bay-functionalized tetraazaperylenes by Zr-mediated cyclization and four-fold Suzuki–Miyaura cross coupling. In the Zr-mediated approach, an η4-cyclobutadiene-zirconium(IV) complex was isolated as an intermediate to cyclobutene-annulated de... |
Feb 12, 2024 - SFB 1249: N-Heteropolyzyklen als Funktionsmaterialien - B: Theory & Structure
Stein, Arnulf; Rolf, Daniela; Lotze, Christian; Günther, Benjamin; Gade, Lutz H.; Franke, Katharina J.; Tegeder, Petra, 2024, "Band Formation at Interfaces Between N-Heteropolycycles and Gold Electrodes [research data]", https://doi.org/10.11588/data/QNAPNN, heiDATA, V1
Underlying data for figures in the paper "Band Formation at Interfaces Between N-Heteropolycycles and Gold Electrodes" |
