Yersin, Hartmut and Humbs, W. and Strasser, J. (1997) Low-lying electronic states of [Rh(bpy)₃]³⁺, [Pt(bpy)₂]²⁺, and [Ru(bpy)₃]²⁺. A comparative study based on highly resolved and time-resolved spectra. Coordination Chemistry Reviews 159, pp. 325-358.
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Optical emission and excitation spectra of [Rh(bpy-h₈)₃]³⁺, [Rh(bpy-h₈)₂(bpy-d₈)]³⁺, [Rh(bpy-d₈)₃]³⁺, [Pt(bpy-h₈)₂]²⁺, [Pt(bpy-h₈)(bpy-d₈)]²⁺, [Pt(bpy-d₈)₂]²⁺, [Ru(bpy-h₈)₃]²⁺ [Ru(bpy-h₈)₂(bpy-d₈)]²⁺, and [Ru(bpy-d₈)₃]²⁺ are discussed. A series of trends - also including [Os(bpy)₃]²⁺ - is uncovered. These trends, which are connected with an increase in metal-d or MLCT character in the lowest triplet states, can for instance be seen in transition energies, emission lifetimes, zero-field splittings, rates of spin-lattice relaxation, vibronic satellite structures, and changes of nuclear equilibrium positions on excitation. Moreover, the compounds investigated are also appropriate for consideration of the concept of "dual emission", the relation between MLCT character and covalency, as well as the current models of localization/delocalization. In particular, a comparison of the properties of [Rh(bpy)₃]³⁺- and [Ru(bpy)₃]²⁺- doped [Zn(bpy)₃](ClO₄)₂ provides illustrative and very strong evidence for covalent delocalization in the lowest excited states of [Ru(bpy)₃]²⁺, while ligand-centered localization is found in the states of [Rh(bpy)₃]³⁺. Misinterpretations might occur if the aggregation effects of the chromophores are not taken into account.
|Institutions:||Chemistry and Pharmacy > Institut für Physikalische und Theoretische Chemie > Chair of Chemistry III - Physical Chemistry (Light and Matter) > Prof. Dr. Hartmut Yersin|
|Subjects:||500 Science > 540 Chemistry & allied sciences|
|Refereed:||Yes, this version has been refereed|
|Created at the University of Regensburg:||Yes|
|Owner:||Prof. Dr. Hartmut Yersin|
|Deposited On:||11 Feb 2011 11:30|
|Last Modified:||11 Feb 2011 11:30|
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