Abstract
Catalytic methane oxidation was conducted using a μ-nitrido-bridged dinuclear iron complex of a four-fold rotaxane heterodimer of a porphyrin and a phthalocyanine. Extension of the π-stacked structure of the four-fold rotaxane-based μ-nitrido-bridged iron porphyrinoid dimer by supramolecular complexation with an additional tetraanionic porphyrin apparently increased the methane conversion ability.
| Original language | English |
|---|---|
| Pages (from-to) | 11477-11482 |
| Number of pages | 6 |
| Journal | New Journal of Chemistry |
| Volume | 43 |
| Issue number | 29 |
| DOIs | |
| Publication status | Published - 2019 |
All Science Journal Classification (ASJC) codes
- Catalysis
- Chemistry(all)
- Materials Chemistry
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Cite this
Yamada, Y., Morita, K., Mihara, N., Igawa, K., Tomooka, K., & Tanaka, K. (2019). Catalytic methane oxidation by a supramolecular conjugate based on a μ-nitrido-bridged iron porphyrinoid dimer. New Journal of Chemistry, 43(29), 11477-11482. https://doi.org/10.1039/c9nj02210d