Difference in Kinetic Behavior on the Photosensitized Decomposition of the Tris(oxalato)cobaltate(III) Ion by Tris(2,2′-bipyridine)ruthenium(II) and Bis(3,3′-biisoquinoline) (2,2′-bipyridine)ruthenium(II)
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/64/4/64_4_1401/_pdf
Reference7 articles.
1. Tris (2,2'-bipyridine)ruthenium(II) sensitized reactions of some oxalato complexes
2. Light-induced electron-transfer reactions. Part 2. Kinetics of the intra-molecular redox decomposition of tris(oxalato)-cobaltate(III) by irradiation with visible light of aqueous solution containing tris(2,2′-bipyridine)ruthenium(II) ion
3. Luminescence of ruthenium(II) tris chelate complexes containing the ligands 2,2'-bipyridine and 2,2'-biisoquinoline. Behavior of the Ru(bpy)2+ and Ru(bpy)22+ emitting units
4. 2,2'-Bipyridine Complexes. I. Polarized Crystal Spectra of Tris (2,2'-bipyridine)copper(II), -nickel(II), -cobalt(II), -iron(II), and -ruthenium(II)
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1. Ruthenium;Coordination Chemistry Reviews;1994-03
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