| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7756717 | Journal of Organometallic Chemistry | 2015 | 6 Pages |
Abstract
A redox-induced intramolecular C-N bond was formed in an azopyridylruthenium complex with the terminal CO ligand. The reduction product was isolated and fully characterized. The reversible protection-deprotection of the CO moiety by redox reactions led to a large difference in photoreactivity of the coordinated carbonyl.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Dai Oyama, Bisa Mun, Tsugiko Takase,