Exploring the localized to delocalized transition in non-symmetric bimetallic ruthenium polypyridines
Author:
Affiliation:
1. Universidad de Buenos Aires
2. Facultad de Ciencias Exactas y Naturales
3. Departamento de Química Inorgánica
4. Analítica y Química Física
5. Buenos Aires
Abstract
Modification of the ligand L in the mixed-valence cyanide-bridged complexes [Ru(tpy)(bpy)(μ-CN)Ru(bpy)2(L)]3+/4+ (L= Cl− (12+), NCS− (23+), 4-dimethylaminopyridine (34+) or acetonitrile (44+)) reduces the difference between the redox potentials of the ruthenium ions and leads to a transition from a localized to a delocalized configuration.
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/DT/C7DT02422C
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