Dinitrogen-bridged diruthenium complexes bearing 2,6-pyridinedicarboxylate in the mixed-valence state
A dinitrogen-bridged diruthenium complex bearing 2,6-pyridine-dicarboxylate (pydc<sup>2-</sup>), which coordinates in a κ<sup>2</sup>-<i>ON</i> bidentate mode, with ammine and hydroxido ligands has been synthesized by reactions of ruthenium(III) and/or ruthenium(II) complexes with hydrazine or dinitrogen as a dinitrogen source. A reaction of the diruthenium complex with pyridine affords a pyridine-substituted diruthenium complex. The electronic structures of the diruthenium complexes in a mixed-valence state have been investigated using UV-vis-NIR and IR spectroscopy and electrochemical methods.
Authors
- Hirotaka Nagao (ORCID: https://orcid.org/0000-0001-9630-7602)
- Tomoyo Misawa‐Suzuki (ORCID: https://orcid.org/0000-0002-2848-5412)
- Nayoung Kim (ORCID: https://orcid.org/0000-0002-9397-0406)
- Masami Otsuka
- K. Uehara
- Aya Benzaki
Institutions
- Sophia University (JP)
Publication Details
- Journal
- Dalton Transactions
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5dt02337h
- Primary Topic
- Organometallic Complex Synthesis and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Society for the Promotion of Science