1 to 10 of 38 Results
Mar 26, 2024
Hüßler, Christopher; Dietl, Martin C.; Kahle, Justin; Lopes, Eric F.; Kawamura, Miku; Krämer, Petra; Rominger, Frank; Rudolph, Matthias; Hachida, Iwao; Hashmi, A. Stephen K., 2024, "Synthesis and structural properties of para-diselenopyrazines [data]", https://doi.org/10.11588/data/UYS0N6, heiDATA, V1
Recently, dithienopyrazines have emerged as promising building blocks in the field of materials science, showcasing their potential as hole-transport materials in organic electronic devices. Herein, we report the synthesis of its heavier analogues, the diselenopyrazines, along wi... |
Mar 20, 2024 - Institute of Organic Chemistry - AK Mastalerz
Yang, Xuan; Brückner, Margit; Rominger, Frank; Kirschbaum, Tobias; Mastalerz, Michael, 2024, "Dispersion-Driven Formation of Chiral Twisted PAH Double Helices [Data]", https://doi.org/10.11588/data/BRM2DI, heiDATA, V1
Molecular double helices are ubiquitous in nature and have also been generated artificially. These are usually based on helical ribbons. Here, a new type of double helices based on twisted ribbons is introduced. The monomeric strands are polycyclic aromatic hydrocarbons of variou... |
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 22, 2024 - Institute of Organic Chemistry - AK Mastalerz
Keck, Christoph; Rominger, Frank; Mastalerz, Michael, 2024, "Synthesis of Chiral Pyrene-Based 1,4-Dithiins [Data]", https://doi.org/10.11588/data/NCRUAV, heiDATA, V1
The 1,4-dithiin motif is known for its reversible redox properties to generate radical cations and diradical dications and thus is interesting for organic electronic applications. However, examples where this motif is embedded into chiral larger fused aromatic compounds is very r... |
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 1, 2024 - Bunz Group
Zong, Wansheng; Hippchen, Nikolai; Nico, Zeitter; Maier, Steffen; Philipp, Ludwig; Rominger, Frank; Freudenberg, Jan; Bunz, Uwe H. F., 2024, "Stable Azaheptacenes", https://doi.org/10.11588/data/P9AVCU, heiDATA, V1
we have developed a novel access to stable azaheptacenes and investigated both their (air-stable) radical anions as well as dianions. The two azaheptacenes are significantly more stable than reported examples. We identified their structure through NMR, IR, MS and X-ray crystallog... |
Jan 31, 2024
Hashmi, A. Stephen K.; Hüßler, Christopher; Kahle, Justin; Dietl, Martin C.; Krämer, Petra; Rominger, Frank; Rudolph, Matthias, 2024, "Facile two-step Synthesis of para-Dithienopyrazines [data]", https://doi.org/10.11588/data/14RXKL, heiDATA, V1
N-Heteropolycyclic compounds are valuable building blocks in organic electronic devices. In this work, a convenient route for the synthesis of para-dithienopyrazines from readily available starting materials is described. A cascade of nucleophilic aromatic substitution and subseq... |
Jan 25, 2024 - Bunz Group
Ludwig, Philipp; Rominger, Frank; Freudenberg, Jan; Bunz, Uwe H. F., 2024, "Stabilization of Acenes: “Geländer”-Pentacenes [data]", https://doi.org/10.11588/data/NITIKZ, heiDATA, V1
We report soluble tetrakis-biphenyl substituted pentacenes comprised of sp2 carbons and synthesized from pentacene-5,7,12,14-tetraone. Intramolecular Yamamoto coupling of two tetrakis(chlorobiphenylyl)pentacenes yields helical, doubly wrapped pentacenes, in which the quaterphenyl... |
