Surface Coordination of Nitric Oxide to a Self-Assembled Monolayer of a Triruthenium Cluster: An in Situ Infrared Spectroscopic Study
Author:
Affiliation:
1. Catalysis Research Center, Hokkaido University, Sapporo 001-0021, Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810, and PRESTO, Japan Science and Technology Agency (JST), Tokyo 102-0075, Japan
Publisher
American Chemical Society (ACS)
Subject
Electrochemistry,Spectroscopy,Surfaces and Interfaces,Condensed Matter Physics,General Materials Science
Link
https://pubs.acs.org/doi/pdf/10.1021/la800374s
Reference42 articles.
1. Oxidation state properties of delocalized, ligand-bridged metal complexes. [Ru3O(CH3CO2)6L3]n+ and the pyrazine-bridged, cluster-cluster dimer, [Ru3O(CH3CO2)6(py)2]2pyzm+
2. Electronic structure and redox properties of the clusters [Ru3O(CH3CO2)6L3]n+
3. Spectroelectrochemistry and cyclic voltammetry of the trinuclear [Ru3O(O2CCH3)6(pyrazine)3] cluster
4. Reversible Multi-Step and Multielectron Redox Behavior of the Oxo-Centered Trinuclear Ruthenium Complex with Redox-Active Ligand, [Ru3(.mu.3-O)(.mu.-CH3CO2)6(mbpy+)3]4+ (mbpy+ = N-Methyl-4,4'-bipyridinium Ion) and Its Trirhodium and Diruthenium-Rhodium Derivatives
5. Oxo-Centered Mixed-Ligand Triruthenium Complexes Having Redox-Active N-Methyl-4,4‘-bipyridinium Ions (mbpy+). Reversible Multistep Electrochemical Properties of [RuIII2RuII(μ3-O)(μ-CH3CO2)6(mbpy+)2(CO)]2+ and [RuIII3(μ3-O)(μ-CH3CO2)6(mbpy+)2(L)]3+ (L = H2O and N-Heterocyclic Ligands)
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