Triptycepenes: Synthesis, Metal Complexes, and Their Reactivity in Catalytic Reactions
An efficient protocol allows the convenient synthesis of substituted triptycepenes through the condensation of anthracene α-diketone with 3-pentanone or 1,3-diphenylpropan-2-one, finally yielding the corresponding cyclopentadienones. This approach offers a potential route toward sterically bulky cyclopentadienyl ligand frameworks. The methyl-substituted triptycepene was used to generate η<sup>5</sup>-coordinated Ru and Co complexes as well as an η<sup>4</sup>-coordinated Fe complex. These metal complexes were characterized by single-crystal X-ray diffraction, and their exemplary catalytic activity in metal-catalyzed reactions like cyclotrimerization, C-H functionalization, and transfer hydrogenation was investigated.
Authors
- Marko Hapke (ORCID: https://orcid.org/0000-0001-7454-9184)
- Uwe V. Monkowius (ORCID: https://orcid.org/0000-0003-0662-2866)
- Shyam Sundar Mothuku
Institutions
- Johannes Kepler University of Linz (AT)
- Leibniz Institute for Catalysis (DE)
- Linz Center of Mechatronics (Austria) (AT)
Publication Details
- Journal
- Organometallics
- Published
- 2025-05-29
- DOI
- https://doi.org/10.1021/acs.organomet.5c00102
- Primary Topic
- Porphyrin and Phthalocyanine Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Austrian Science Fund