Michael Giese
Affiliations: | Chemisrty | Universitat Duisburg-Essen |
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Parents
Sign in to add mentor| Markus Albrecht | grad student | RWTH Aachen University | |
| Mark J. MacLachlan | post-doc | UBC |
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Publications
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| Malotke F, Thiele T, Gutmann JS, et al. (2023) Direct Digital Photonic Patterning of Hydrogen-Bonded Cholesteric Liquid-Crystalline Films. Acs Applied Materials & Interfaces |
| Blanke M, Neumann T, Gutierrez Suburu ME, et al. (2022) Tuning the Fluorescence in Dynamic Covalent Bonded Liquid Crystals. Acs Applied Materials & Interfaces. 14: 55864-55872 |
| Blanke M, Postulka L, Ciara I, et al. (2022) Manipulation of Liquid Crystalline Properties by Dynamic Covalent Chemistry─En Route to Adaptive Materials. Acs Applied Materials & Interfaces. 14: 16755-16763 |
| Nath S, Kappelt A, Spengler M, et al. (2021) Tuning the solid-state emission of liquid crystalline nitro-cyanostilbene by halogen bonding. Beilstein Journal of Organic Chemistry. 17: 124-131 |
| Kappelt A, Giese M. (2020) Photo-switchable Fluorescence in Hydrogen-bonded Liquid Crystals. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Giese M, Albrecht M. (2020) Alkyl-Alkyl Interactions in the Periphery of Supramolecular Entities: From the Evaluation of Weak Forces to Applications. Chempluschem. 85: 715-724 |
| Blanke M, Balszuweit J, Saccone M, et al. (2020) Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol. Chemical Communications (Cambridge, England) |
| Saccone M, Pfletscher M, Kather S, et al. (2019) Improving the mesomorphic behaviour of supramolecular liquid crystals by resonance-assisted hydrogen bonding Journal of Materials Chemistry C. 7: 8643-8648 |
| Kapf A, Eslahi H, Blanke M, et al. (2019) Alkyloxy modified pyrene fluorophores with tunable photophysical and crystalline properties New Journal of Chemistry. 43: 6361-6371 |
| Saccone M, Riebe S, Stelzer J, et al. (2019) Structure–property relationships in aromatic thioethers featuring aggregation-induced emission: solid-state structures and theoretical analysis Crystengcomm. 21: 3097-3105 |